TGF-β-induced epithelial to mesenchymal transition
Open accessAbstract
During development and in the context of different morphogenetic events, epithelial cells undergo a process called epithelial to mesenchymal transition or transdifferentiation (EMT). In this process, the cells lose their epithelial characteristics, including their polarity and specialized cell-cell contacts, and acquire a migratory behavior, allowing them to move away from their epithelial cell community and to integrate into surrounding tissue, even at remote locations. EMT illustrates the differentiation plasticity during development and is complemented by another process, called mesenchymal to epithelial transition (MET). While being an integral process during development, EMT is also recapitulated under pathological conditions, prominently in fibrosis and in invasion and metastasis of carcinomas. Accordingly, EMT is considered as an important step in tumor progression. TGF-beta signaling has been shown to play an important role in EMT. In fact, adding TGF-beta to epithelial cells in culture is a convenient way to induce EMT in various epithelial cells. Although much less characterized, epithelial plasticity can also be regulated by TGF-beta-related bone morphogenetic proteins (BMPs), and BMPs have been shown to induce EMT or MET depending on the developmental context. In this review, we will discuss the induction of EMT in response to TGF-beta, and focus on the underlying signaling and transcription mechanisms.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
EMT plays an important role in cancer progression and is induced by TGFβ.
“EMT plays an important role in cancer progression and is induced by TGFβ [23].”
Adding TGF-β induces EMT in diverse epithelial cell cultures via the SMAD signaling pathway.
“Adding TGF-β induces EMT in diverse epithelial cell cultures via the SMAD signaling pathway (56).”
From Tumor-Induced Inflammatory Cytokines and the Emerging Diagnostic Devices for Cancer Detection and Prognosis (2021) · cites this paper as [56]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
1 retracted
Han, S., Ritzenthaler, J. D., Sitaraman, S. V., & Roman, J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m604013200 · Cited by 98 · see citing works
RetractedSmad-dependent and Smad-independent pathways in TGF-β family signalling
Derynck, R., & Zhang, Y. E. (2003) · Nature · doi:10.1038/nature02006 · Cited by 5,370 · see citing works
Self-citationTwist, a Master Regulator of Morphogenesis, Plays an Essential Role in Tumor Metastasis
Yang, J., Mani, S. A., Donaher, J. L., Ramaswamy, S., Itzykson, R., Côme, C., Savagner, P., Gitelman, I., Richardson, A. L., & Weinberg, R. A. (2004) · Cell · doi:10.1016/j.cell.2004.06.006 · Cited by 3,856 · see citing works
Gregory, P. A., Bert, A. G., Paterson, E. L., Barry, S. C., Tsykin, A., Farshid, G., Vadas, M. A., Khew‐Goodall, Y., & Goodall, G. J. (2008) · Nature Cell Biology · doi:10.1038/ncb1722 · Cited by 3,852 · see citing works
Cano, A., Pérez‐Moreno, M., Rodrigo, I., Locascio, A., Blanco, M. J., Barrio, M. G. D., Portillo, F., & Nieto, M. A. (2000) · Nature Cell Biology · doi:10.1038/35000025 · Cited by 3,672 · see citing works
Snail, Zeb and bHLH factors in tumour progression: An alliance against the epithelial phenotype?
Peinado, H., Olmeda, D., & Cano, A. (2007) · Nature reviews. Cancer · doi:10.1038/nrc2131 · Cited by 3,121 · see citing works
Batlle, E., Sancho, E., Francı́, C., Dominguez-Sola, D., Monfar, M., Baulida, J., & de Herreros, A. G. (2000) · Nature Cell Biology · doi:10.1038/35000034 · Cited by 2,671 · see citing works
Convergence of Wnt, ß-Catenin, and Cadherin Pathways
Nelson, W. J., & Nusse, R. (2004) · Science · doi:10.1126/science.1094291 · Cited by 2,515 · see citing works
Multifunctional strands in tight junctions
Tsukita, S., Furuse, M., & Itoh, M. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35067088 · Cited by 2,514 · see citing works
TGF-β Signaling in Tumor Suppression and Cancer Progression
Derynck, R., Akhurst, R. J., & Balmain, A. (2001) · Nature Genetics · doi:10.1038/ng1001-117 · Cited by 2,275 · see citing works
Self-citationPark, S.-M., Gaur, A. B., Lengyel, E., & Peter, M. E. (2008) · Genes & Development · doi:10.1101/gad.1640608 · Cited by 2,272 · see citing works
Endothelial-to-mesenchymal transition contributes to cardiac fibrosis
Zeisberg, E. M., Tarnavski, O., Zeisberg, M., Dorfman, A. L., McMullen, J. R., Gustafsson, E., Chandraker, A. K., Yuan, X., Pu, W. T., Roberts, A. B., et al. (2007) · Nature Medicine · doi:10.1038/nm1613 · Cited by 2,224 · see citing works
The epithelial–mesenchymal transition: new insights in signaling, development, and disease
Lee, J. M., Dedhar, S., Kalluri, R., & Thompson, E. W. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200601018 · Cited by 2,018 · see citing works
SPECIFICITY AND VERSATILITY IN TGF-β SIGNALING THROUGH SMADS
Feng, X.-H., & Derynck, R. (2005) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.21.022404.142018 · Cited by 1,869 · see citing works
Self-citationEvidence that fibroblasts derive from epithelium during tissue fibrosis
Iwano, M., Plieth, D., Danoff, T. M., Xue, C., Okada, H., & Neilson, E. G. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15518 · Cited by 1,809 · see citing works
Helix-Loop-Helix Proteins: Regulators of Transcription in Eucaryotic Organisms
Massari, M. E., & Murre, C. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.2.429-440.2000 · Cited by 1,800 · see citing works
The snail superfamily of zinc-finger transcription factors
Nieto, M. A. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm757 · Cited by 1,719 · see citing works
Korpal, M., Lee, E. S., Hu, G., & Kang, Y. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.c800074200 · Cited by 1,642 · see citing works
Evidence that fibroblasts derive from epithelium during tissue fibrosis
Iwano, M., Plieth, D., Danoff, T. M., Xue, C., Okada, H., & Neilson, E. G. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215518 · Cited by 1,589 · see citing works
TGF-β and epithelial-to-mesenchymal transitions
Zavadil, J., & Böttinger, E. P. (2005) · Oncogene · doi:10.1038/sj.onc.1208927 · Cited by 1,580 · see citing works
Growing roles for the mTOR pathway
Sarbassov, D. D., Ali, S. M., & Sabatini, D. M. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.09.009 · Cited by 1,556 · see citing works
The two-handed E box binding zinc finger protein SIP1 downregulates E-cadherin and induces invasion.
Comijn, J., Berx, G., Vermassen, P., Verschueren, K., van Grunsven, L. V., Bruyneel, E., Mareel, M., Huylebroeck, D., & van Roy, F. (2001) · Molecules and Cells · doi:10.1016/s1097-2765(01)00260-x · Cited by 1,464 · see citing works
The Snail genes as inducers of cell movement and survival: implications in development and cancer
Barrallo‐Gimeno, A., & Nieto, M. A. (2005) · Development · doi:10.1242/dev.01907 · Cited by 1,396 · see citing works
Cell adhesion and signalling by cadherins and Ig-CAMs in cancer
Cavallaro, U., & Christofori, G. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1276 · Cited by 1,314 · see citing works
Bolós, V., Peinado, H., Pérez‐Moreno, M., Fraga, M. F., Esteller, M., & Cano, A. (2002) · Journal of Cell Science · doi:10.1242/jcs.00224 · Cited by 1,100 · see citing works
Epithelial—mesenchymal and mesenchymal—epithelial transitions in carcinoma progression
Hugo, H. J., Ackland, M. L., Blick, T., Lawrence, M. G., Clements, J. A., Williams, E. D., & Thompson, E. W. (2007) · Journal of Cellular Physiology · doi:10.1002/jcp.21223 · Cited by 1,091 · see citing works
Bhowmick, N., Ghiassi, M., Bakin, A. V., Aakre, M., Lundquist, C., Engel, M., Arteaga, C., & Moses, H. (2001) · Molecular Biology of the Cell · doi:10.1091/mbc.12.1.27 · Cited by 1,087 · see citing works
TGF-β-induced EMT: mechanisms and implications for fibrotic lung disease
Willis, B. C., & Borok, Z. (2007) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00163.2007 · Cited by 1,044 · see citing works
The SLUG zinc-finger protein represses E-cadherin in breast cancer.
Hajra, K. M., Chen, D. Y., & Fearon, E. R. (2002) · PubMed · Cited by 1,004 · see citing works
A mechanism of repression of TGFbeta / Smad signaling by oncogenic RasPreprint
Kretzschmar, M., Doody, J. F., Timokhina, I., & Massagué, J. (1999) · Genes & Development · doi:10.1101/gad.13.7.804 · Cited by 997 · see citing works
Bakin, A. V., Tomlinson, A. K., Bhowmick, N. A., Moses, H. L., & Arteaga, C. L. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m005912200 · Cited by 993 · see citing works
Timmerman, L., Grego‐Bessa, J., Raya, Á., Bertrán, E., Pérez-Pomares, J. M., Díez, J., Aranda, S., Palomo‐Ponce, S., McCormick, F., Izpisúa‐Belmonte, J. C., et al. (2003) · Genes & Development · doi:10.1101/gad.276304 · Cited by 986 · see citing works
Miettinen, P. J., Ebner, R., Lopez, A. R., & Derynck, R. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.127.6.2021 · Cited by 939 · see citing works
Self-citationMice lacking Smad3 show accelerated wound healing and an impaired local inflammatory response
Ashcroft, G. S., Yang, X., Glick, A. B., Weinstein, M., Letterio, J. J., Mizel, D. E., Anzano, M., Greenwell-Wild, T., Wahl, S. M., Deng, C., et al. (1999) · Nature Cell Biology · doi:10.1038/12971 · Cited by 911 · see citing works
Regulation of the Polarity Protein Par6 by TGFß Receptors Controls Epithelial Cell Plasticity
Ozdamar, B., Bose, R., Barrios-Rodiles, M., Wang, H.-R., Zhang, Y., & Wrana, J. L. (2005) · Science · doi:10.1126/science.1105718 · Cited by 881 · see citing works
Sato, M., Muragaki, Y., Saika, S., Roberts, A. B., & Ooshima, A. (2003) · Journal of Clinical Investigation · doi:10.1172/jci19270 · Cited by 831 · see citing works
Eger, A., Aigner, K., Sonderegger, S., Dampier, B., Oehler, S., Schreiber, M., Berx, G., Cano, A., Beug, H., & Foisner, R. (2005) · Oncogene · doi:10.1038/sj.onc.1208429 · Cited by 808 · see citing works
Moustakas, A., & Heldin, C. (2007) · Cancer Science · doi:10.1111/j.1349-7006.2007.00550.x · Cited by 798 · see citing works
Roles of TGF-beta in hepatic fibrosis
Gressner, A. M. (2002) · Frontiers in bioscience · doi:10.2741/a812 · Cited by 785 · see citing works
Structure and Function of the Cell Surface (Tethered) Mucins
Hattrup, C. L., & Gendler, S. J. (2007) · Annual Review of Physiology · doi:10.1146/annurev.physiol.70.113006.100659 · Cited by 781 · see citing works
Peritoneal Dialysis and Epithelial-to-Mesenchymal Transition of Mesothelial Cells
Yáñez‐Mó, M., Lara‐Pezzi, E., Selgas, R., Ramírez‐Huesca, M., Domı́nguez-Jiménez, C., Jiménez-Heffernan, J. A., Aguilera, A. I., Sánchez-Tomero, J. A., Bajo, M. A., Álvarez, V., et al. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa020809 · Cited by 778 · see citing works
Control of Cell Behavior During Vertebrate Development by Slug , a Zinc Finger Gene
Nieto, M. A., Sargent, M. G., Wilkinson, D. G., & Cooke, J. (1994) · Science · doi:10.1126/science.7513443 · Cited by 770 · see citing works
Integration of TGF‐β/Smad and Jagged1/Notch signalling in epithelial‐to‐mesenchymal transition
Zavadil, J., C̆ermák, L., Soto-Nieves, N., & Böttinger, E. P. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600069 · Cited by 747 · see citing works
TGF‐β receptor‐activated p38 MAP kinase mediates Smad‐independent TGF‐β responses
Yu, L., DeRouen, M. C., & Zhang, Y. E. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf366 · Cited by 721 · see citing works
Ansieau, S., Bastid, J., Doreau, A., Morel, A., Bouchet, B. P., Thomas, C., Fauvet, F., Puisieux, I., Doglioni, C., Piccinin, S., et al. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.06.005 · Cited by 713 · see citing works
Ras and TGFβ cooperatively regulate epithelial cell plasticity and metastasis
Janda, E., Lehmann, K. E., Killisch, I., Jechlinger, M., Herzig, M., Downward, J., Beug, H., & Grünert, S. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200109037 · Cited by 702 · see citing works
Pellegrin, S., & Mellor, H. (2007) · Journal of Cell Science · doi:10.1242/jcs.018473 · Cited by 700 · see citing works
Sato, M., Muragaki, Y., Saika, S., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319270 · Cited by 686 · see citing works
Ikenouchi, J., Matsuda, M., Furuse, M., & Tsukita, S. (2003) · Journal of Cell Science · doi:10.1242/jcs.00389 · Cited by 678 · see citing works
Diverse cellular and molecular mechanisms contribute to epithelial plasticity and metastasis
Grünert, S., Jechlinger, M., & Beug, H. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1175 · Cited by 677 · see citing works
Bardeesy, N., Cheng, K.-H., Berger, J. H., Chu, G. C., Pahler, J., Olson, P., Hezel, A. F., Horner, J., Lauwers, G. Y., Hanahan, D., et al. (2006) · Genes & Development · doi:10.1101/gad.1478706 · Cited by 674 · see citing works
Cadherins as Modulators of Cellular Phenotype
Wheelock, M. J., & Johnson, K. R. (2003) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.19.011102.111135 · Cited by 673 · see citing works
Armstrong, E. J., & Bischoff, J. E. (2004) · Circulation Research · doi:10.1161/01.res.0000141146.95728.da · Cited by 648 · see citing works
Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome
Howard, T. D., Paznekas, W. A., Green, E. D., Chiang, L. C., Ma, N. S. F., Luna, R. I. O. D., Delgado, C. G., Gonzalez-Ramos, M., Kline, A. D., & Jabs, E. W. (1997) · Nature Genetics · doi:10.1038/ng0197-36 · Cited by 645 · see citing works
Transforming Growth Factor β-1 Induces Snail Transcription Factor in Epithelial Cell Lines
Peinado, H., Quintanilla, M., & Cano, A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211304200 · Cited by 642 · see citing works
Mutations of the TWIST gene in the Saethre-Chotzene syndrome
Ghouzzi, V. E., Merrer, M. F. L., Perrin‐Schmitt, F., Lajeunie, E., Bénit, P., Rénier, D., Bourgeois, P., Bolcato‐Bellemin, A., Münnich, A., & Bonaventure, J. (1997) · Nature Genetics · doi:10.1038/ng0197-42 · Cited by 639 · see citing works
Cui, W., Fowlis, D. J., Bryson, S., Duffie, E., Ireland, H., Balmain, A., & Akhurst, R. J. (1996) · Cell · doi:10.1016/s0092-8674(00)80127-0 · Cited by 628 · see citing works
TGFβ signaling is necessary for carcinoma cell invasiveness and metastasis
Oft, M., Heider, K., & Beug, H. (1998) · Current Biology · doi:10.1016/s0960-9822(07)00533-7 · Cited by 624 · see citing works
The Mouse Snail Gene Encodes a Key Regulator of the Epithelial-Mesenchymal Transition
Carver, E. A., Jiang, R., Lan, Y., Oram, K. F., & Gridley, T. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.23.8184-8188.2001 · Cited by 624 · see citing works
Aigner, K., Dampier, B., Descovich, L., Mikula, M., Sultan, A., Schreiber, M., Mikulits, W., Brabletz, T., Strand, D., Obrist, P., et al. (2007) · Oncogene · doi:10.1038/sj.onc.1210508 · Cited by 618 · see citing works
twist is required in head mesenchyme for cranial neural tube morphogenesis.Preprint
Chen, Z., & Behringer, R. R. (1995) · Genes & Development · doi:10.1101/gad.9.6.686 · Cited by 616 · see citing works
Valcourt, U., Kowanetz, M., Niimi, H., Heldin, C., & Moustakas, A. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-08-0658 · Cited by 611 · see citing works
Desmosome structure, composition and function
Garrod, D. R., & Chidgey, M. (2007) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2007.07.014 · Cited by 581 · see citing works
TGF‐β activates Erk MAP kinase signalling through direct phosphorylation of ShcA
Lee, M. K., Pardoux, C., Hall, M. C., Lee, P. S., Warburton, D., Qing, J., Smith, S. M., & Derynck, R. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601818 · Cited by 580 · see citing works
Self-citationMechanisms, mechanics and function of epithelial–mesenchymal transitions in early development
Shook, D. R., & Keller, R. E. (2003) · Mechanisms of Development · doi:10.1016/j.mod.2003.06.005 · Cited by 577 · see citing works
Lamouille, S., & Derynck, R. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200611146 · Cited by 573 · see citing works
Self-citationTRAF6 Mediates Smad-Independent Activation of JNK and p38 by TGF-β
Yamashita, M., Fátyol, K., Jin, C., Wang, X., Liu, Z.-G., & Zhang, Y. E. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.09.002 · Cited by 559 · see citing works
The type I TGF-β receptor engages TRAF6 to activate TAK1 in a receptor kinase-independent manner
Sorrentino, A., Thakur, N., Grimsby, S., Marcusson, A., von Bülow, V., Schuster, N., Zhang, S., Heldin, C., & Landström, M. (2008) · Nature Cell Biology · doi:10.1038/ncb1780 · Cited by 553 · see citing works
A Self-Enabling TGFβ Response Coupled to Stress Signaling
Kang, Y., Chen, C.-R., & Massagué, J. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00109-6 · Cited by 548 · see citing works
SIP1/ZEB2 induces EMT by repressing genes of different epithelial cell-cell junctions
Vandewalle, C. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki965 · Cited by 546 · see citing works
The Transcriptional Repressor ZEB1 Promotes Metastasis and Loss of Cell Polarity in Cancer
Spaderna, S., Schmalhofer, O., Wahlbuhl, M., Dimmler, A. W., Bauer, K., Sultan, A., Hlubek, F., Jung, A., Strand, D. J., Eger, A., et al. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-5682 · Cited by 532 · see citing works
Activation of the Erk Pathway Is Required for TGF-β1-Induced EMT In Vitro
Xie, L., Law, B. K., Chytil, A. M., Brown, K. A., Aakre, M. E., & Moses, H. L. (2004) · Neoplasia · doi:10.1593/neo.04241 · Cited by 523 · see citing works
Savagner, P., Yamada, K. M., & Thiery, J. P. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.137.6.1403 · Cited by 520 · see citing works
Guaita, S., Puig, I., Francı́, C., Garrido, M., Dominguez-Sola, D., Batlle, E., Sancho, E., Dedhar, S., de Herreros, A. G., & Baulida, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m206400200 · Cited by 501 · see citing works
Transforming growth factor-β employs HMGA2 to elicit epithelial–mesenchymal transition
Thuault, S., Valcourt, U., Petersen, M., Manfioletti, G., Heldin, C., & Moustakas, A. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200512110 · Cited by 500 · see citing works
Assémat, E., Bazellières, E., Pallesi‐Pocachard, E., Bivic, A. L., & Massey‐Harroche, D. (2007) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2007.08.029 · Cited by 471 · see citing works
Pérez‐Moreno, M., Locascio, A., Rodrigo, I., Dhondt, G., Portillo, F., Nieto, M. A., & Cano, A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100827200 · Cited by 440 · see citing works
Bakin, A. V., Rinehart, C., Tomlinson, A. K., & Arteaga, C. L. (2002) · Journal of Cell Science · doi:10.1242/jcs.115.15.3193 · Cited by 430 · see citing works
Piek, E., Moustakas, A., Kurisaki, A., Heldin, C., & ten Dijke, P. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.24.4557 · Cited by 427 · see citing works
Postigo, A. A., Depp, J. L., Taylor, J. J., & Kroll, K. L. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg226 · Cited by 388 · see citing works
Deckers, M., van Dinther, M., Buijs, J., Que, I., Löwik, C., van der Pluijm, G., & ten Dijke, P. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-3560 · Cited by 379 · see citing works
Liebner, S., Cattelino, A., Gallini, R., Rudini, N., Iurlaro, M., Piccolo, S., & Dejana, E. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200403050 · Cited by 376 · see citing works
Metastasis is driven by sequential elevation of H-ras and Smad2 levels
Oft, M., Akhurst, R. J., & Balmain, A. (2002) · Nature Cell Biology · doi:10.1038/ncb807 · Cited by 372 · see citing works
Hepatocyte growth factor induces cell scattering through MAPK/Egr‐1‐mediated upregulation of Snail
Grotegut, S., von Schweinitz, D., Christofori, G., & Lehembre, F. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601213 · Cited by 364 · see citing works
Evidence for a function of CtBP in epithelial gene regulation and anoikis
Grooteclaes, M., & Frisch, S. M. (2000) · Oncogene · doi:10.1038/sj.onc.1203721 · Cited by 355 · see citing works
Kaimori, A., Potter, J. J., Kaimori, J.-Y., Wang, C., Mezey, E., & Koteish, A. A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700998200 · Cited by 354 · see citing works
Kowanetz, M., Valcourt, U., Bergström, R., Heldin, C., & Moustakas, A. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.10.4241-4254.2004 · Cited by 346 · see citing works
ATF-2 Is a Common Nuclear Target of Smad and TAK1 Pathways in Transforming Growth Factor-β Signaling
Sano, Y., Harada, J., Tashiro, S., Goto‐Mandeville, R., Maekawa, T., & Ishii, S. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.13.8949 · Cited by 345 · see citing works
Kajita, M., McClinic, K. N., & Wade, P. A. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.17.7559-7566.2004 · Cited by 334 · see citing works
Snail activation disrupts tissue homeostasis and induces fibrosis in the adult kidney
Boutet, A., de Frutos, C. A., Maxwell, P. H., Mayol, M. J., Romero, J., & Nieto, M. A. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601421 · Cited by 327 · see citing works
Ohkubo, T., & Ozawa, M. (2004) · Journal of Cell Science · doi:10.1242/jcs.01004 · Cited by 322 · see citing works
Shirakihara, T., Saitoh, M., & Miyazono, K. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-03-0249 · Cited by 322 · see citing works
Moreno‐Bueno, G., Cubillo, E., Sarrió, D., Peinado, H., Rodríguez-Pinilla, S. M., Villa, S., Bolós, V., Jordà, M., Fabra, À., Portillo, F., et al. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-0479 · Cited by 320 · see citing works
TGF-β signal transduction and mesangial cell fibrogenesis
Schnaper, H. W., Hayashida, T., Hubchak, S. C., & Poncelet, A.-C. (2003) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00300.2002 · Cited by 312 · see citing works
Exploring a New Twist on Tumor Metastasis
Yang, J., Mani, S. A., & Weinberg, R. A. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-3850 · Cited by 297 · see citing works
Opposing functions of ZEB proteins in the regulation of the TGFβ/BMP signaling pathway
Postigo, A. A. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg225 · Cited by 295 · see citing works
Lehmann, K. E., Janda, E., Pierreux, C. E., Rytömaa, M., Schulze, A., McMahon, M., Hill, C. S., Beug, H., & Downward, J. (2000) · Genes & Development · doi:10.1101/gad.181700 · Cited by 287 · see citing works
Molecular components of the adherens junction
Niessen, C. M., & Gottardi, C. J. (2008) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2007.12.015 · Cited by 283 · see citing works
Dooley, S., Hamzavi, J., Ciuclan, L. I., Godoy, P., Ilkavets, I., Ehnert, S., Ueberham, E., Gebhardt, R., Kanzler, S., Geier, A., et al. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.04.038 · Cited by 280 · see citing works
Snail silencing effectively suppresses tumour growth and invasiveness
Olmeda, D., Jordà, M., Peinado, H., Fabra, À., & Cano, A. (2006) · Oncogene · doi:10.1038/sj.onc.1209997 · Cited by 265 · see citing works
BMP signaling and early embryonic patterning
Kishigami, S., & Mishina, Y. M. (2005) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2005.04.002 · Cited by 265 · see citing works
Morita, T., Mayanagi, T., & Sobue, K. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200708174 · Cited by 262 · see citing works
Snail and Slug are major determinants of ovarian cancer invasiveness at the transcription level
Kurrey, N. K., Amit, K., & Bapat, S. A. (2005) · Gynecologic Oncology · doi:10.1016/j.ygyno.2004.12.043 · Cited by 261 · see citing works
Regulation of cell polarity during epithelial morphogenesis
Martín‐Belmonte, F., & Mostov, K. E. (2008) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2008.01.001 · Cited by 257 · see citing works
Craene, B. D., Gilbert, B., Stove, C. P., Bruyneel, E. A., Roy, F. M. V., & Berx, G. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-3545 · Cited by 254 · see citing works
Davies, M., Robinson, M., Smith, E., Huntley, S. P., Prime, S. S., & Paterson, I. C. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20458 · Cited by 250 · see citing works
Galliher, A. J., & Schiemann, W. P. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-3851 · Cited by 249 · see citing works
Jordà, M., Olmeda, D., Vinyals, A., Valero, E., Cubillo, E., Llorens, A., Cano, A., & Fabra, À. (2005) · Journal of Cell Science · doi:10.1242/jcs.02465 · Cited by 234 · see citing works
Type I Transforming Growth Factor β Receptor Binds to and Activates Phosphatidylinositol 3-Kinase
Yi, J. Y., Shin, I., & Arteaga, C. L. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413223200 · Cited by 228 · see citing works
Transforming growth factor beta in cardiovascular development and function
Azhar, M., Schultz, J. E. J., Grupp, I. L., Dorn, G. W., Meneton, P., Molin, D. G. M., Groot, A. C. G., & Doetschman, T. (2003) · Cytokine & Growth Factor Reviews · doi:10.1016/s1359-6101(03)00044-3 · Cited by 228 · see citing works
Han, G. (2005) · Journal of Clinical Investigation · doi:10.1172/jci24399 · Cited by 224 · see citing works
Grände, M., Franzén, Å., Karlsson, J.-O., Ericson, L. E., Heldin, N., & Nilsson, M. (2002) · Journal of Cell Science · doi:10.1242/jcs.00091 · Cited by 215 · see citing works
Hoot, K. E., Lighthall, J. G., Han, G., Lu, S., Li, A., Ju, W., Kulesz-Martin, M. F., Böttinger, E. P., & Wang, X.-J. (2008) · Journal of Clinical Investigation · doi:10.1172/jci33713 · Cited by 209 · see citing works
Regulation of desmosome assembly and adhesion
Yin, T., & Green, K. J. (2004) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2004.09.005 · Cited by 199 · see citing works
Modulation of Smad2-mediated Signaling by Extracellular Signal-regulated Kinase
Funaba, M., Zimmerman, C. M., & Mathews, L. S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204597200 · Cited by 196 · see citing works
Whiteman, E. L., Liu, C.-J., Fearon, E. R., & Margolis, B. L. (2008) · Oncogene · doi:10.1038/onc.2008.9 · Cited by 195 · see citing works
Differential expression of genes encoding TGFs β1, β2, and β3 during murine palate formation
Pelton, R. W., Hogan, B. L. M., Miller, D. A., & Moses, H. L. (1990) · Developmental Biology · doi:10.1016/0012-1606(90)90401-4 · Cited by 192 · see citing works
Nawshad, A., LaGamba, D., & Hay, E. D. (2004) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2004.05.007 · Cited by 189 · see citing works
Wang, W., Zhou, G., Hu, M. C. ‐., Yao, Z., & Tan, T. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.36.22771 · Cited by 188 · see citing works
Portella, G., Cumming, S. A., Liddell, J., Cui, W., Ireland, H., Akhurst, R. J., & Balmain, A. (1998) · PubMed · Cited by 185 · see citing works
Slug is an Essential Target of TGFβ2 Signaling in the Developing Chicken Heart
Romano, L. A., & Runyan, R. B. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9750 · Cited by 184 · see citing works
Vardouli, L., Moustakas, A., & Stournaras, C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m402651200 · Cited by 182 · see citing works
Regulation of vimentin by SIP1 in human epithelial breast tumor cells
Bindels, S., Mestdagt, M., Vandewalle, C., Jacobs, N., Volders, L., Noël, A., Roy, F. M. V., Berx, G., Foidart, J. M., & Gilles, C. (2006) · Oncogene · doi:10.1038/sj.onc.1209511 · Cited by 182 · see citing works
Cho, H. J., Baek, K. E., Saika, S., Jeong, M., & Yoo, J. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.12.035 · Cited by 177 · see citing works
Nawshad, A., Medici, D., Liu, C.-C., & Hay, E. D. (2007) · Journal of Cell Science · doi:10.1242/jcs.003129 · Cited by 156 · see citing works
Deletion of Smad2 in Mouse Liver Reveals Novel Functions in Hepatocyte Growth and Differentiation
Ju, W., Ogawa, A., Heyer, J., Nierhof, D., Yu, L., Kucherlapati, R., Shafritz, D. A., & Böttinger, E. P. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.26.2.654-667.2006 · Cited by 153 · see citing works
Mercado-Pimentel, M. E., & Runyan, R. B. (2007) · Cells Tissues Organs · doi:10.1159/000101315 · Cited by 152 · see citing works
Long, J., Zuo, D., & Park, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504477200 · Cited by 150 · see citing works
Eger, A., Stockinger, A., Park, J., Langkopf, E., Mikula, M., Gotzmann, J., Mikulits, W., Beug, H., & Foisner, R. (2004) · Oncogene · doi:10.1038/sj.onc.1207416 · Cited by 148 · see citing works
A Signaling Pathway Involving TGF-β2 and Snail in Hair Follicle Morphogenesis
Jamora, C., Lee, P., Kocieniewski, P., Azhar, M., Hosokawa, R., Chai, Y., & Fuchs, E. V. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0030011 · Cited by 148 · see citing works
Uttamsingh, S., Bao, X., Nguyen, K. T., Bhanot, M., Gong, J., Chan, J., Liu, F., Chu, T.-Y., & Wang, L. (2007) · Oncogene · doi:10.1038/sj.onc.1210915 · Cited by 146 · see citing works
δEF1 Mediates TGF-β Signaling in Vascular Smooth Muscle Cell Differentiation
Nishimura, G., Manabe, I., Tsushima, K., Fujiu, K., Oishi, Y., Imai, Y., Maemura, K., Miyagishi, M., Higashi, Y., Kondoh, H., et al. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.05.011 · Cited by 143 · see citing works
A role for Id in the regulation of TGF-β-induced epithelial–mesenchymal transdifferentiation
Kondo, M., Cubillo, E., Tobiume, K., Shirakihara, T., Fukuda, N., Suzuki, H. I., Shimizu, K., Takehara, K., Cano, A., Saitoh, M., et al. (2004) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401467 · Cited by 143 · see citing works
Human Slug Is a Repressor That Localizes to Sites of Active Transcription
Hemavathy, K. C., Guru, S. C., Harris, J., Chen, J. D., & Ip, Y. T. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.14.5087-5095.2000 · Cited by 136 · see citing works
Regulation of desmosome assembly and adhesion
Yin, T., & Green, K. J. (2004) · Seminars in Cell and Developmental Biology · doi:10.1016/s1084-9521(04)00091-6 · Cited by 135 · see citing works
Kattla, J. J., Carew, R. M., Heljić, M., Godson, C., & Brazil, D. P. (2008) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00548.2007 · Cited by 130 · see citing works
Jun N-terminal kinase 1 regulates epithelial-to-mesenchymal transition induced by TGF-β1
Alcorn, J. F., Guala, A. S., van der Velden, J. L. J., McElhinney, B., Irvin, C. G., Davis, R. J., & Janssen-Heininger, Y. M. W. (2008) · Journal of Cell Science · doi:10.1242/jcs.019455 · Cited by 128 · see citing works
Grego-Bessa, J., Díez, J., & de la Pompa, J. L. (2004) · Cell Cycle · doi:10.4161/cc.3.6.949 · Cited by 120 · see citing works
Zeisberg, E. M., Tarnavski, O., Zeisberg, M., Dorfman, A. L., McMullen, J. R., Gustafsson, E., Chandraker, A. K., Yuan, X., Pu, W. T., Roberts, A. B., et al. (2007) · Cited by 119 · see citing works
Snail family members and cell survival in physiological and pathological cleft palates
Martínez‐Álvarez, C., Blanco, M. J., Pérez-Gómez, R., Rabadán, M. A., Aparicio, M. E., Resel, E., Martı́nez, T., & Nieto, M. A. (2003) · Developmental Biology · doi:10.1016/j.ydbio.2003.09.022 · Cited by 117 · see citing works
Pon, Y. L., Zhou, H. Y., Cheung, A., Ngan, H., & Wong, A. S. T. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-6302 · Cited by 115 · see citing works
Santibanez, J. F. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.09.003 · Cited by 108 · see citing works
Taki, M., Verschueren, K., Yokoyama, K., Nagayama, M., & Kamata, N. (2006) · International Journal of Oncology · doi:10.3892/ijo.28.2.487 · Cited by 93 · see citing works
TGFβ Activated Kinase-1: New Insights into the Diverse Roles of TAK1 in Development and Immunity
Delaney, J. R., & Mlodzik, M. (2006) · Cell Cycle · doi:10.4161/cc.5.24.3558 · Cited by 91 · see citing works
Rodríguez‐Barbero, A., Dorado, F., Velasco, S., Pandiella, A., Banas, B., & López-Novoa, J. M. (2006) · Kidney International · doi:10.1038/sj.ki.5001626 · Cited by 89 · see citing works
Saika, S., Ikeda, K., Yamanaka, O., Sato, M., Muragaki, Y., Ohnishi, Y., Ooshima, A., Nakajima, Y., Namikawa, K., Kiyama, H., et al. (2004) · Laboratory Investigation · doi:10.1038/labinvest.3700151 · Cited by 88 · see citing works
Desgrosellier, J. S., Mundell, N. A., McDonnell, M. A., Moses, H. L., & Barnett, J. V. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2004.12.037 · Cited by 88 · see citing works
Llorens, A., Rodrigo, I., Lopez-Barcons, L. A., González-Garrigues, M., Lozano, E., Vinyals, A., Quintanilla, M., Cano, A., & Fabra, À. (1998) · PubMed · Cited by 86 · see citing works
Lien, S.-C., Usami, S., Chien, S., & Chiu, J. (2005) · Cellular Signalling · doi:10.1016/j.cellsig.2005.10.013 · Cited by 84 · see citing works
Imamichi, Y., & Menke, A. (2007) · Cells Tissues Organs · doi:10.1159/000101319 · Cited by 84 · see citing works
Cho, H. J., & Yoo, J. (2007) · Cell Biology International · doi:10.1016/j.cellbi.2007.04.006 · Cited by 82 · see citing works
Wang, Z., Wade, P. A., Mandell, K. J., Akyildiz, A., Parkos, C. A., Mrsny, R. J., & Nusrat, A. (2006) · Oncogene · doi:10.1038/sj.onc.1209902 · Cited by 79 · see citing works
Tavares, A. L. P., Mercado-Pimentel, M. E., Runyan, R. B., & Kitten, G. T. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20771 · Cited by 76 · see citing works
Snail controls differentiation of hepatocytes by repressing HNF4α expression
Cicchini, C., Filippini, D., Coen, S., Marchetti, A., Cavallari, C., Laudadio, I., Spagnoli, F. M., Alonzi, T., & Tripodi, M. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20730 · Cited by 75 · see citing works
Endoglin and Alk5 regulate epithelial–mesenchymal transformation during cardiac valve formation
Mercado-Pimentel, M. E., Hubbard, A. D., & Runyan, R. B. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.12.038 · Cited by 75 · see citing works
Navarro, P., Lozano, E., & Cano, A. (1993) · Journal of Cell Science · doi:10.1242/jcs.105.4.923 · Cited by 70 · see citing works
Yeh, Y.-Y., Chiao, C.-C., Kuo, W.-Y., Hsiao, Y., Chen, Y., Wei, Y., Lai, T.-H., Fong, Y., & Tang, C. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.11.017 · Cited by 70 · see citing works
Zhao, Y., Min, C., Vora, S. R., Trackman, P. C., Sonenshein, G. E., & Kirsch, K. H. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m802612200 · Cited by 65 · see citing works
The Müllerian Duct: Recent Insights into Its Development and Regression
Klattig, J., & Englert, C. (2007) · Sexual Development · doi:10.1159/000108929 · Cited by 64 · see citing works
Lin, C.-C., Chiang, L.-L., Lin, C., Shih, C.-H., Liao, Y., Hsu, M., & Chen, B.-C. (2007) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.01.025 · Cited by 62 · see citing works
Liu, Q., Mao, H., Nie, J., Chen, W., Yang, Q., Dong, X., & Yu, X. (2008) · Peritoneal Dialysis International · doi:10.1177/089686080802803s18 · Cited by 60 · see citing works
Lee, Y.-I., Kwon, Y.-J., & Joo, C. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.02.150 · Cited by 53 · see citing works
Takano, S., Kanai, F., Jazag, A., Ijichi, H., Yao, J. Q., Ogawa, H., Enomoto, N., Omata, M., & Nakao, A. (2006) · The Journal of Biochemistry · doi:10.1093/jb/mvm039 · Cited by 48 · see citing works
Reactivation of Snail Genes in Renal Fibrosis and Carcinomas: A Process of Reversed Embryogenesis?
Boutet, A., Esteban, M. A., Maxwell, P. H., & Nieto, M. A. (2007) · Cell Cycle · doi:10.4161/cc.6.6.4022 · Cited by 47 · see citing works
Marchetti, A., Colletti, M., Cozzolino, A. M., Steindler, C., Lunadei, M., Mancone, C., & Tripodi, M. (2008) · Cellular Signalling · doi:10.1016/j.cellsig.2008.08.002 · Cited by 45 · see citing works
Activity‐induced fiber regeneration in rat soleus muscle
Wanek, L., & Snow, M. H. (2000) · The Anatomical Record · doi:10.1002/(sici)1097-0185(20000201)258:2 · Cited by 43 · see citing works
Schmidt, C. R., Gi, Y. J., Patel, T. A., Coffey, R. J., Beauchamp, R. D., & Pearson, A. S. (2005) · Surgery · doi:10.1016/j.surg.2005.06.007 · Cited by 36 · see citing works
Frame, M. C., & Inman, G. J. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.09.016 · Cited by 29 · see citing works
Xu, G., Li, Q., Cao, X.-X., Chen, Q., Zhao, Z., Diao, Z.-Q., & Xu, Z. (2007) · Cellular & Molecular Biology Letters · doi:10.2478/s11658-007-0018-x · Cited by 19 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [1]Akhurst R Derynck R Miyazono K TGF-β signaling in epithelial-mesenchymal transition and invasion and metastasis. The TGF-beta family 2007 939 964 Cold Spring Harbor Laboratory Press New York
Cited by
Sorted by citations
Molecular mechanisms of epithelial–mesenchymal transition
Lamouille, S., Xu, J., & Derynck, R. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3758 · Cited by 8,091 · see citing works
Self-citationThe extracellular matrix at a glance
Frantz, C., Stewart, K. M., & Weaver, V. M. (2010) · Journal of Cell Science · doi:10.1242/jcs.023820 · Cited by 4,334 · see citing works
New insights into the mechanisms of epithelial–mesenchymal transition and implications for cancer
Dongre, A., & Weinberg, R. A. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0080-4 · Cited by 3,876 · see citing works
EMT, CSCs, and drug resistance: the mechanistic link and clinical implications
Shibue, T., & Weinberg, R. A. (2017) · Nature Reviews Clinical Oncology · doi:10.1038/nrclinonc.2017.44 · Cited by 2,539 · see citing works
Brabletz, T., Kalluri, R., Nieto, M. A., & Weinberg, R. A. (2018) · Nature Reviews Cancer · doi:10.1038/nrc.2017.118 · Cited by 1,961 · see citing works
Chronic inflammation and cytokines in the tumor microenvironment
Landskron, G., De la Fuente, M., Thuwajit, P., Thuwajit, C., & Hermoso, M. A. (2014) · Journal of Immunology Research · doi:10.1155/2014/149185 · Cited by 1,765 · see citing works
Long-Term Culture of Genome-Stable Bipotent Stem Cells from Adult Human Liver
Huch, M., Gehart, H., van Boxtel, R., Hamer, K., Blokzijl, F., Verstegen, M. M. A., Ellis, E., van Wenum, M., Fuchs, S. A., de Ligt, J., et al. (2015) · Cell · doi:10.1016/j.cell.2014.11.050 · Cited by 1,619 · see citing works
Loh, C.-Y., Chai, J., Tang, T. F., Wong, W. F., Sethi, G., Shanmugam, M. K., Chong, P. P., & Looi, C. Y. (2019) · Cells · doi:10.3390/cells8101118 · Cited by 1,323 · see citing works
Biernacka, A., Dobaczewski, M. P., & Frangogiannis, N. G. (2011) · Growth Factors · doi:10.3109/08977194.2011.595714 · Cited by 1,175 · see citing works
TGFβ signalling: a complex web in cancer progression
Ikushima, H., & Miyazono, K. (2010) · Nature reviews. Cancer · doi:10.1038/nrc2853 · Cited by 1,170 · see citing works
Exosomes in cancer development, metastasis, and drug resistance: a comprehensive review
Azmi, A. S., Bao, B., & Sarkar, F. H. (2013) · Cancer and Metastasis Reviews · doi:10.1007/s10555-013-9441-9 · Cited by 1,159 · see citing works
Epithelial-Mesenchymal Transition in Cancer: A Historical Overview
Ribatti, D., Tamma, R., & Annese, T. (2020) · Translational Oncology · doi:10.1016/j.tranon.2020.100773 · Cited by 1,012 · see citing works
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome
Huttlin, E. L., Bruckner, R. J., Navarrete-Perea, J., Cannon, J. R., Baltier, K., Gebreab, F., Gygi, M. P., Thornock, A., Zarraga, G., Tam, S., et al. (2020) · doi:10.1101/2020.01.19.905109 · Cited by 960 · see citing works
Wei, S. C., Fattet, L., Tsai, J. H., Guo, Y., Pai, V. H., Majeski, H. E., Chen, A. C., Sah, R. L., Taylor, S. S., Engler, A. J., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3157 · Cited by 934 · see citing works
The Role of Snail in EMT and Tumorigenesis
Wang, Y., Shi, J., Chai, K., Ying, X., & Zhou, B. P. (2013) · Current Cancer Drug Targets · doi:10.2174/15680096113136660102 · Cited by 871 · see citing works
Proteogenomic Characterization Reveals Therapeutic Vulnerabilities in Lung Adenocarcinoma
Gillette, M. A., Satpathy, S., Cao, S., Dhanasekaran, S. M., Vasaikar, S. V., Krug, K., Petralia, F., Li, Y., Liang, W.-W., Reva, B., et al. (2020) · Cell · doi:10.1016/j.cell.2020.06.013 · Cited by 820 · see citing works
Pathogenic mechanisms in HBV- and HCV-associated hepatocellular carcinoma
Arzumanyan, A. L., Reis, H. M. G. P. V., & Feitelson, M. A. (2013) · Nature reviews. Cancer · doi:10.1038/nrc3449 · Cited by 801 · see citing works
TGF-β signaling and epithelial–mesenchymal transition in cancer progression
Katsuno, Y., Lamouille, S., & Derynck, R. (2012) · Current Opinion in Oncology · doi:10.1097/cco.0b013e32835b6371 · Cited by 785 · see citing works
Self-citationSkin Acute Wound Healing: A Comprehensive Review
Cañedo‐Dorantes, L., & Cañedo-Ayala, M. (2019) · International Journal of Inflammation · doi:10.1155/2019/3706315 · Cited by 712 · see citing works
Metastatic Stem Cells: Sources, Niches, and Vital Pathways
Óskarsson, T., Batlle, E., & Massagué, J. (2014) · Cell stem cell · doi:10.1016/j.stem.2014.02.002 · Cited by 702 · see citing works
Epithelial-to-mesenchymal transition in cancer: complexity and opportunities
Zhang, Y., & Weinberg, R. A. (2018) · Frontiers of Medicine · doi:10.1007/s11684-018-0656-6 · Cited by 660 · see citing works
Georgoudaki, A.-M., Prokopec, K. E., Boura, V. F., Hellqvist, E., Sohn, S., Östling, J., Dahan, R., Harris, R. A., Rantalainen, M., Klevebring, D., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.04.084 · Cited by 609 · see citing works
Wang, L., Cho, K. B., Li, Y., Tao, G., Xie, Z.-X., & Guo, B. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20225758 · Cited by 552 · see citing works
Subramanyam, D., Lamouille, S., Judson, R. L., Liu, J. Y., Bucay, N., Derynck, R., & Blelloch, R. H. (2011) · Nature Biotechnology · doi:10.1038/nbt.1862 · Cited by 594 · see citing works
Self-citationTGF-β/BMP signaling and other molecular events: regulation of osteoblastogenesis and bone formation
Rahman, M. S., Akhtar, N., Jamil, H. M., Banik, R. S., & Asaduzzaman, S. M. (2015) · Bone Research · doi:10.1038/boneres.2015.5 · Cited by 585 · see citing works
Zhang, F., Wang, H., Wang, X., Jiang, G., Liu, H., Zhang, G., Wang, H., Fang, R., Bu, X., Cai, S., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.10561 · Cited by 580 · see citing works
Epithelial-mesenchymal transition in tissue repair and fibrosis
Stone, R. C., Pastar, I., Ojeh, N. O., Chen, V., Liu, S., Garzon, K. I., & Tomic‐Canic, M. (2016) · Cell and Tissue Research · doi:10.1007/s00441-016-2464-0 · Cited by 577 · see citing works
Erin, N., Grahovac, J., Brozovic, A., & Efferth, T. (2020) · Drug Resistance Updates · doi:10.1016/j.drup.2020.100715 · Cited by 527 · see citing works
Regulation of Transforming Growth Factor-β1–driven Lung Fibrosis by Galectin-3
MacKinnon, A. C., Gibbons, M., Farnworth, S. L., Leffler, H., Nilsson, U. J., Delaine, T., Simpson, A. J., Forbes, S. J., Hirani, N., Gauldie, J., et al. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201106-0965oc · Cited by 520 · see citing works
A Comprehensive Roadmap of Murine Spermatogenesis Defined by Single-Cell RNA-Seq
Green, C. D., Ma, Q., Manske, G. L., Shami, A. N., Zheng, X., Marini, S., Moritz, L., Sultan, C., Gurczynski, S. J., Moore, B. B., et al. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.07.025 · Cited by 515 · see citing works
TGF-β Family Signaling in Tumor Suppression and Cancer ProgressionPreprint
Seoane, J., & Gomis, R. R. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a022277 · Cited by 512 · see citing works
The Role of Cytokines in Breast Cancer Development and Progression
Esquivel‐Velázquez, M., Ostoa‐Saloma, P., Arreola, M. I. P., Castro, K. E. N., Castro, J. I., & Morales‐Montor, J. (2014) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2014.0026 · Cited by 495 · see citing works
Mechanisms of vasculogenic mimicry in hypoxic tumor microenvironments
Wei, X., Chen, Y., Jiang, X., Miao, P., Liu, Y., Mo, Y., Ren, D., Hua, Y., Yu, B., Zhou, Y., et al. (2021) · Molecular Cancer · doi:10.1186/s12943-020-01288-1 · Cited by 465 · see citing works
Yuan, S., Norgard, R. J., & Stanger, B. Z. (2019) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-0015 · Cited by 458 · see citing works
Tubuloids derived from human adult kidney and urine for personalized disease modeling
Schutgens, F., Rookmaaker, M. B., Margaritis, T., Rios, A. C., Ammerlaan, C. M. E., Jansen, J., Gijzen, L., Vormann, M. K., Vonk, A. M., Viveen, M. C., et al. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0048-8 · Cited by 450 · see citing works
The Role of the Anti-Inflammatory Cytokine Interleukin-10 in Tissue Fibrosis
Steen, E. H., Wang, X., Balaji, S., Butte, M. J., Bollyky, P. L., & Keswani, S. G. (2019) · Advances in Wound Care · doi:10.1089/wound.2019.1032 · Cited by 442 · see citing works
TGF-β signalling and its role in cancer progression and metastasis
Drabsch, Y., & ten Dijke, P. (2012) · Cancer and Metastasis Reviews · doi:10.1007/s10555-012-9375-7 · Cited by 430 · see citing works
Ortiz-Montero, P., Londoño-Vallejo, A., & Vernot, J.-P. (2017) · Cell Communication and Signaling · doi:10.1186/s12964-017-0172-3 · Cited by 428 · see citing works
Immune evasion in cancer: mechanisms and cutting-edge therapeutic approaches
Tufail, M., Jiang, C., & Li, N. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02280-1 · Cited by 424 · see citing works
Transforming growth factor‐β in stem cells and tissue homeostasis
Xu, X., Zheng, L., Yuan, Q., Zhen, G., Crane, J. L., Zhou, X., & Cao, X. (2018) · Bone Research · doi:10.1038/s41413-017-0005-4 · Cited by 414 · see citing works
The dynamic roles of TGF‐β in cancer
Meulmeester, E., & ten Dijke, P. (2010) · The Journal of Pathology · doi:10.1002/path.2785 · Cited by 391 · see citing works
Right Versus Left Colon Cancer Biology: Integrating the Consensus Molecular Subtypes
Lee, M. S., Menter, D. G., & Kopetz, S. (2017) · Journal of the National Comprehensive Cancer Network · doi:10.6004/jnccn.2017.0038 · Cited by 386 · see citing works
Genome-scale epigenetic reprogramming during epithelial-to-mesenchymal transition
McDonald, O. G., Wu, H., Timp, W., Doi, A., & Feinberg, A. P. (2011) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2084 · Cited by 380 · see citing works
Mi, S., Li, Z., Yang, H.-Z., Liu, H., Wang, J.-P., Ma, Y.-G., Wang, X.-X., Liu, H.-Z., Sun, W., & Hu, Z.-W. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1004081 · Cited by 370 · see citing works
TGF-β-Induced Endothelial-Mesenchymal Transition in Fibrotic Diseases
Pardali, E., Sánchez‐Duffhues, G., Gomez‐Puerto, M. C., & ten Dijke, P. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102157 · Cited by 360 · see citing works
Roles of macrophages in tumor development: a spatiotemporal perspective
Bied, M., Ho, W. W., Ginhoux, F., & Blériot, C. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-01061-6 · Cited by 360 · see citing works
The ID proteins: master regulators of cancer stem cells and tumour aggressiveness
Lasorella, A., Benezra, R., & Iavarone, A. (2014) · Nature reviews. Cancer · doi:10.1038/nrc3638 · Cited by 356 · see citing works
The Dual Role of TGFβ in Human Cancer: From Tumor Suppression to Cancer Metastasis
Neel, J.-C., Humbert, L., & Lebrun, J. J. (2012) · ISRN Molecular Biology · doi:10.5402/2012/381428 · Cited by 353 · see citing works
Dávalos, V., Moutinho, C., Villanueva, A., Boqué-Sastre, R., Silva, P., Carneiro, F., & Esteller, M. (2011) · Oncogene · doi:10.1038/onc.2011.383 · Cited by 349 · see citing works
Tumor-associated macrophages: an effective player of the tumor microenvironment
Basak, U., Sarkar, T., Mukherjee, S., Chakraborty, S., Dutta, A., Dutta, S., Nayak, D., Kaushik, S., Das, T., & Sa, G. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1295257 · Cited by 346 · see citing works
Kartikasari, A. E. R., Huertas, C. S., Mitchell, A., & Plebanski, M. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.692142 · Cited by 343 · see citing works
TGF-beta in CAF-mediated tumor growth and metastasis
Calon, A., Tauriello, D. V. F., & Batlle, E. (2014) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2013.12.008 · Cited by 342 · see citing works
Regulation of endothelial cell plasticity by TGF-β
van Meeteren, L. A., & ten Dijke, P. (2011) · Cell and Tissue Research · doi:10.1007/s00441-011-1222-6 · Cited by 335 · see citing works
Stromal features are predictive of disease mortality in oral cancer patients
Marsh, D. J., Suchak, K., Moutasim, K. A., Vallath, S., Hopper, C., Jerjes, W., Upile, T., Kalavrezos, N., Violette, S. M., Weinreb, P. H., et al. (2010) · The Journal of Pathology · doi:10.1002/path.2830 · Cited by 333 · see citing works
Signal Transduction Pathways of EMT Induced by TGF-β, SHH, and WNT and Their Crosstalks
Zhang, J., Tian, X., & Xing, J. (2016) · Journal of Clinical Medicine · doi:10.3390/jcm5040041 · Cited by 328 · see citing works
Natural Killer–Derived Exosomal miR-186 Inhibits Neuroblastoma Growth and Immune Escape Mechanisms
Neviani, P., Wise, P. M., Murtadha, M., Liu, C. W., Wu, C., Jong, A., Seeger, R. C., & Fabbri, M. (2018) · Cancer Research · doi:10.1158/0008-5472.can-18-0779 · Cited by 325 · see citing works
USP4 is regulated by AKT phosphorylation and directly deubiquitylates TGF-β type I receptor
Zhang, L., Zhou, F., Drabsch, Y., Gao, R., Snaar-Jagalska, E. B., Mickanin, C., Huang, H., Sheppard, K.-A., Porter, J. A., Lu, C., et al. (2012) · Nature Cell Biology · doi:10.1038/ncb2522 · Cited by 322 · see citing works
Clements, M., Byrne, E., Guerrero, C., Cattin, A.-L., Zakka, L., Ashraf, A., Burden, J. J., Khadayate, S. P., Lloyd, A. C., Marguerat, S., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.008 · Cited by 322 · see citing works
The pro-metastasis effect of circANKS1B in breast cancer
Zeng, K., He, B., Yang, B. B., Xu, T., Chen, X., Xu, M., Liu, X., Sun, H., Pan, Y., & Wang, S. (2018) · Molecular Cancer · doi:10.1186/s12943-018-0914-x · Cited by 319 · see citing works
Epithelial-mesenchymal Transition and Cell Invasion
Son, H., & Moon, A. (2010) · Toxicological Research · doi:10.5487/tr.2010.26.4.245 · Cited by 318 · see citing works
Shirure, V. S., Bi, Y., Curtis, M. B., Lezia, A., Goedegebuure, M. M., Goedegebuure, S. P., Aft, R., Fields, R. C., & George, S. C. (2018) · Lab on a Chip · doi:10.1039/c8lc00596f · Cited by 316 · see citing works
Fuxe, J., Vincent, C. T., & de Herreros, A. G. (2010) · Cell Cycle · doi:10.4161/cc.9.12.12050 · Cited by 311 · see citing works
Lamouille, S., Connolly, E. C., Smyth, J. W., Akhurst, R. J., & Derynck, R. (2012) · Journal of Cell Science · doi:10.1242/jcs.095299 · Cited by 310 · see citing works
Self-citationKim, D., Xing, T., Yang, Z., Dudek, R. W., Lu, Q., & Chen, Y. (2017) · Journal of Clinical Medicine · doi:10.3390/jcm7010001 · Cited by 308 · see citing works
Matrix metalloproteinases in tumorigenesis: an evolving paradigm
Hua, H., Li, M., Luo, T. L., Yin, Y., & Jiang, Y. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0763-x · Cited by 297 · see citing works
Kumarswamy, R., Mudduluru, G., Ceppi, P., Muppala, S., Kozłowski, M., Nikliński, J., Papotti, M. G., & Allgayer, H. (2011) · International Journal of Cancer · doi:10.1002/ijc.26218 · Cited by 295 · see citing works
Mechanisms that link the oncogenic epithelial–mesenchymal transition to suppression of anoikis
Frisch, S. M., Schaller, M. D., & Cieply, B. W. (2013) · Journal of Cell Science · doi:10.1242/jcs.120907 · Cited by 295 · see citing works
MiR-1 and miR-200 inhibit EMT via Slug-dependent and tumorigenesis via Slug-independent mechanisms
Liu, Y.-N., Yin, J., Abou-Kheir, W. G., Hynes, P. G., Casey, O. M., Fang, L., Yi, M., Stephens, R. M., Seng, V., Sheppard, H., et al. (2012) · Oncogene · doi:10.1038/onc.2012.58 · Cited by 294 · see citing works
Matrix abnormalities in pulmonary fibrosis
Upagupta, C., Shimbori, C., Alsilmi, R. A., & Kolb, M. R. J. (2018) · European Respiratory Review · doi:10.1183/16000617.0033-2018 · Cited by 287 · see citing works
Xu, J., Liu, D., Niu, H., Zhu, G., Xu, Y., Ye, D., Li, J., & Zhang, Q. (2017) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-016-0487-8 · Cited by 285 · see citing works
Self-citationC-Reactive Protein and Cancer—Diagnostic and Therapeutic Insights
Hart, P. C., Rajab, I. M., Alebraheem, M., & Potempa, L. A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.595835 · Cited by 285 · see citing works
Acute Inflammation in Tissue Healing
Soliman, A. M., & Barreda, D. R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010641 · Cited by 283 · see citing works
Autophagy-Dependent Production of Secreted Factors Facilitates Oncogenic RAS-Driven Invasion
Lock, R., Kenific, C. M., Leidal, A. M., Salas, E., & Debnath, J. (2014) · Cancer Discovery · doi:10.1158/2159-8290.cd-13-0841 · Cited by 280 · see citing works
Li, J., Yang, B., Zhou, Q., Wu, Y., Shang, D., Guo, Y., Song, Z., Zheng, Q., & Xiong, J. (2013) · Carcinogenesis · doi:10.1093/carcin/bgt063 · Cited by 280 · see citing works
Pang, M.-F., Georgoudaki, A.-M., Lambut, L., Johansson, J., Tabor, V., Hagikura, K., Jin, Y., Jansson, M., Alexander, J., Nelson, C. M., et al. (2015) · Oncogene · doi:10.1038/onc.2015.133 · Cited by 279 · see citing works
Lysyl Oxidase, Extracellular Matrix Remodeling and Cancer Metastasis
Xiao, Q., & Ge, G. (2012) · Cancer Microenvironment · doi:10.1007/s12307-012-0105-z · Cited by 277 · see citing works
Epithelial-mesenchymal transition in gastric cancer.
Huang, L., Wu, R., & Xu, A. (2015) · PubMed Central · Cited by 276 · see citing works
Li, T., Xie, J., Shen, C., Cheng, D., Shi, Y., Wu, Z., Deng, X., Chen, H., Shen, B., Peng, C., et al. (2015) · Oncogene · doi:10.1038/onc.2015.223 · Cited by 271 · see citing works
RetractedMicrobiome, inflammation and colorectal cancer
Chen, J., Pitmon, E., & Wang, K. (2017) · Seminars in Immunology · doi:10.1016/j.smim.2017.09.006 · Cited by 267 · see citing works
miR-21 and miR-31 Converge on TIAM1 to Regulate Migration and Invasion of Colon Carcinoma Cells
Cottonham, C., Kaneko, S., & Xu, L. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.160069 · Cited by 265 · see citing works
Signaling interplay between transforming growth factor-β receptor and PI3K/AKT pathways in cancer
Zhang, L., Zhou, F., & ten Dijke, P. (2013) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2013.10.001 · Cited by 265 · see citing works
SOX4 Induces Epithelial–Mesenchymal Transition and Contributes to Breast Cancer Progression
Zhang, J., Liang, Q. Y., Yang, L., Yao, M., Li, L., Gao, X., Feng, J., Zhang, Y., Gao, H., Liu, D., et al. (2012) · Cancer Research · doi:10.1158/0008-5472.can-12-1045 · Cited by 262 · see citing works
Inherited human diseases of heterotopic bone formation
Shore, E. M., & Kaplan, F. S. (2010) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2010.122 · Cited by 261 · see citing works
Cancer Risk After Use of Recombinant Bone Morphogenetic Protein-2 for Spinal Arthrodesis
Carragee, E. J., Chu, G., Rohatgi, R., Hurwitz, E. L., Weiner, B. K., Yoon, S. T., Comer, G. C., & Kopjar, B. (2013) · Journal of Bone and Joint Surgery · doi:10.2106/jbjs.l.01483 · Cited by 261 · see citing works
Tumor promoting roles of IL-10, TGF-β, IL-4, and IL-35: Its implications in cancer immunotherapy
Mirlekar, B. (2022) · SAGE Open Medicine · doi:10.1177/20503121211069012 · Cited by 261 · see citing works
Phosphorylation of eIF4E promotes EMT and metastasis via translational control of SNAIL and MMP-3
Robichaud, N., Rincon, S. V. D., Huor, B., Alain, T., Petruccelli, L. A., Hearnden, J., Gonçalves, C., Grotegut, S., Spruck, C., Furic, L., et al. (2014) · Oncogene · doi:10.1038/onc.2014.146 · Cited by 259 · see citing works
Pregnancy-associated miRNA-clusters
Prieto, D. M. M., Ospina‐Prieto, S., Chaiwangyen, W., Schönleben, M., & Markert, U. R. (2013) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2012.11.001 · Cited by 258 · see citing works
Participation of miR-200 in Pulmonary Fibrosis
Yang, S., Banerjee, S., de Freitas, A., Sanders, Y. Y., Ding, Q., Matalon, S., Thannickal, V. J., Abraham, E. H., & Liu, G. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.10.005 · Cited by 258 · see citing works
Mica, Y., Lee, G., Chambers, S. M., Tomishima, M., & Studer, L. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.03.025 · Cited by 246 · see citing works
Regulation of epithelial–mesenchymal and mesenchymal–epithelial transitions by microRNAs
Lamouille, S., Subramanyam, D., Blelloch, R. H., & Derynck, R. (2013) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2013.01.008 · Cited by 257 · see citing works
Self-citationTumor cell plasticity in targeted therapy-induced resistance: Mechanisms and new strategies
Shi, Z.-D., Pang, K., Wu, Z.-X., Dong, Y., Hao, L., Qin, J.-X., Wang, W., Chen, Z.-S., & Han, C.-H. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01383-x · Cited by 256 · see citing works
The emerging role of TGF-β superfamily coreceptors in cancer
Bernabéu, C., López-Novoa, J. M., & Quintanilla, M. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.07.003 · Cited by 254 · see citing works
Role of TGF-β in Skin Chronic Wounds: A Keratinocyte Perspective
Liarte, S., Bernabé‐García, Á., & Nicolás, F. J. (2020) · Cells · doi:10.3390/cells9020306 · Cited by 251 · see citing works
Cancer Stemness Meets Immunity: From Mechanism to Therapy
Chen, P., Hsu, W., Han, J., Xia, Y., & DePinho, R. A. (2021) · Cell Reports · doi:10.1016/j.celrep.2020.108597 · Cited by 251 · see citing works
Deshmukh, A. P., Vasaikar, S. V., Tomczak, K. J., Tripathi, S., den Hollander, P., Arslan, E., Chakraborty, P., Soundararajan, R., Jolly, M. K., Rai, K., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2102050118 · Cited by 249 · see citing works
The Role of Cancer-Associated Fibroblasts in Cancer Invasion and Metastasis
Asif, P. J., Longobardi, C., Hahne, M., & Medema, J. P. (2021) · Cancers · doi:10.3390/cancers13184720 · Cited by 245 · see citing works
Ghahhari, N. M., & Babashah, S. (2015) · European Journal of Cancer · doi:10.1016/j.ejca.2015.04.021 · Cited by 243 · see citing works
Haynes, J., Srivastava, J., Madson, N., Wittmann, T., & Barber, D. L. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-02-0119 · Cited by 241 · see citing works
Loret, N., Denys, H. G., Tummers, P., & Berx, G. (2019) · Cancers · doi:10.3390/cancers11060838 · Cited by 241 · see citing works
Inflammatory cytokines in the pathogenesis of cardiovascular disease and cancer
Amin, M. N., Siddiqui, S. A., Ibrahim, M., Hakim, M. L., Ahammed, M. S., Kabir, A., & Sultana, F. (2020) · SAGE Open Medicine · doi:10.1177/2050312120965752 · Cited by 236 · see citing works
- Authors
- Xu, J., Lamouille, S., & Derynck, R.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Derynck, Rik
- Venue
- Cell Research
- Published
- 2009-01-20
- Volume
- 19
- Issue
- 2
- Pages
- 156-172
- ISSN
- 1001-0602 (ISSN-L)
- 1748-7838
- PMC
- PMC4720263
- OpenAlex
- W1760215417
- Cited by
- 2,804
- References
- 167
- Citations by year
- 2026: 123 · 2025: 178 · 2024: 186 · 2023: 207 · 2022: 252 · 2021: 242 · 2020: 220 · 2019: 174 · 2018: 190 · 2017: 197 · 2016: 162 · 2015: 148 · 2014: 149 · 2013: 111 · 2012: 95
- FWCI
- 6.73
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cell Research (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (P01HL060231)
- National Center for Research Resources (P41RR001614)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- epithelial-mesenchymal transition, TGF-beta signaling, mesenchymal-epithelial transition, epithelial plasticity, bone morphogenetic proteins, cell migration, tumor progression, fibrosis, tumor invasion and metastasis, cell polarity, transcriptional regulation
- MeSH terms
- Epithelial Cells, Mesoderm, Transcription Factors, Signal Transduction, Transforming Growth Factor beta, Bone Morphogenetic Proteins, Smad Proteins, Cell Transdifferentiation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review