Cancer Stem Cells and Epithelial-to-Mesenchymal Transition in Cancer Metastasis
Open accessAbstract
The cancer stem cell (CSC) concept stands for undifferentiated tumor cells with the ability to initiate heterogeneous tumors. It is also relevant in metastasis and can explain how metastatic tumors mirror the heterogeneity of primary tumors. Cellular plasticity, including the epithelial-to-mesenchymal transition (EMT), enables the generation of CSCs at different steps of the metastatic process including metastatic colonization. In this review, we update the concept of CSCs and provide evidence of the existence of metastatic stem cells (MetSCs). In addition, we highlight the nuanced understanding of EMT that has been gained recently and the association of mesenchymal-to-epithelial transition (MET) with the acquisition of CSCs properties during metastasis. We also comment on the computational approaches that have profoundly influenced our understanding of CSCs and EMT; and how these studies and new experimental technologies can yield a deeper understanding of the biological aspects of metastasis.
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In multiple carcinoma types, EMT raises the count of cells with cancer stem cell features.
“In a variety of carcinomas, EMT increases the number of carcinoma cells with stem cell properties, i.e. cancer stem cells (CSCs)34,37,127,137.”
From TGFβ biology in cancer progression and immunotherapy (2021) · cites this paper as [137]
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Cites
Prospective identification of tumorigenic breast cancer cells
Al‐Hajj, M., Wicha, M. S., Benito‐Hernández, A., Morrison, S. J., & Clarke, M. F. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0530291100 · Cited by 10,388 · see citing works
The basics of epithelial-mesenchymal transition
Kalluri, R., & Weinberg, R. A. (2009) · Journal of Clinical Investigation · doi:10.1172/jci39104 · Cited by 10,196 · see citing works
Epithelial-Mesenchymal Transitions in Development and Disease
Thiery, J. P., Acloque, H., Huang, R. Y. J., & Nieto, M. A. (2009) · Cell · doi:10.1016/j.cell.2009.11.007 · Cited by 9,931 · see citing works
Stem cells, cancer, and cancer stem cells
Reya, T., Morrison, S. J., Clarke, M. F., & Weissman, I. L. (2001) · Nature · doi:10.1038/35102167 · Cited by 9,738 · see citing works
The Epithelial-Mesenchymal Transition Generates Cells with Properties of Stem Cells
Mani, S. A., Guo, W., Liao, M.-J., Eaton, E. N., Ayyanan, A., Zhou, A. Y., Brooks, M. W., Reinhard, F., Zhang, C. C., Shipitsin, M. V., et al. (2008) · Cell · doi:10.1016/j.cell.2008.03.027 · Cited by 8,679 · see citing works
Bonnet, D., & Dick, J. (1997) · Nature Medicine · doi:10.1038/nm0797-730 · Cited by 7,417 · see citing works
Identification of human brain tumour initiating cells
Singh, S. K., Hawkins, C. E., Clarke, I. D., Squire, J. A., Bayani, J., Hide, T., Henkelman, R. M., Cusimano, M. D., & Dirks, P. B. (2004) · Nature · doi:10.1038/nature03128 · Cited by 7,388 · see citing works
Epithelial–mesenchymal transitions in tumour progression
Thiery, J. P. (2002) · Nature reviews. Cancer · doi:10.1038/nrc822 · Cited by 6,632 · see citing works
Nowell, P. C. (1976) · Science · doi:10.1126/science.959840 · Cited by 6,471 · see citing works
Involvement of chemokine receptors in breast cancer metastasis
Müller, A., Homey, B., Soto, H., Ge, N., Catron, D., Buchanan, M. E., McClanahan, T., Murphy, E., Yuan, W., Wagner, S. N., et al. (2001) · Nature · doi:10.1038/35065016 · Cited by 5,340 · see citing works
Single-cell RNA-seq highlights intratumoral heterogeneity in primary glioblastoma
Patel, A. P., Tirosh, I., Trombetta, J. J., Shalek, A. K., Gillespie, S. M., Wakimoto, H., Cahill, D. P., Nahed, B. V., Curry, W. T., Martuza, R. L., et al. (2014) · Science · doi:10.1126/science.1254257 · Cited by 5,063 · see citing works
Dissecting the multicellular ecosystem of metastatic melanoma by single-cell RNA-seq
Tirosh, I., Izar, B., Prakadan, S. M., Wadsworth, M. H., Treacy, D., Trombetta, J. J., Rotem, A., Rodman, C., Lian, C., Murphy, G., et al. (2016) · Science · doi:10.1126/science.aad0501 · Cited by 4,944 · see citing works
A Perspective on Cancer Cell Metastasis
Chaffer, C. L., & Weinberg, R. A. (2011) · Science · doi:10.1126/science.1203543 · Cited by 4,791 · see citing works
A cell initiating human acute myeloid leukaemia after transplantation into SCID mice
Lapidot, T., Sirard, C., Vormoor, J., Murdoch, B., Hoang, T., Caceres-Cortes, J., Minden, M., Paterson, B., Caligiuri, M. A., & Dick, J. E. (1994) · Nature · doi:10.1038/367645a0 · Cited by 4,783 · see citing works
Nieto, M. A., Huang, R. Y.-J., Jackson, R. A., & Thiery, J. P. (2016) · Cell · doi:10.1016/j.cell.2016.06.028 · Cited by 4,492 · see citing works
Cancer Metastasis: Building a Framework
Gupta, G. P., & Massagué, J. (2006) · Cell · doi:10.1016/j.cell.2006.11.001 · Cited by 4,230 · see citing works
Identification and expansion of human colon-cancer-initiating cells
Ricci‐Vitiani, L., Lombardi, D. G., Pilozzi, E., Biffoni, M., Todaro, M., Peschle, C., & Maria, R. D. (2006) · Nature · doi:10.1038/nature05384 · Cited by 4,001 · see citing works
Dissemination and growth of cancer cells in metastatic sites
Chambers, A. F., Groom, A. C., & MacDonald, I. C. (2002) · Nature reviews. Cancer · doi:10.1038/nrc865 · Cited by 3,920 · 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
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
Wnt signalling in stem cells and cancer
Reya, T., & Clevers, H. (2005) · Nature · doi:10.1038/nature03319 · Cited by 3,666 · see citing works
Emerging Biological Principles of Metastasis
Lambert, A. W., Pattabiraman, D. R., & Weinberg, R. A. (2017) · Cell · doi:10.1016/j.cell.2016.11.037 · Cited by 3,075 · see citing works
Hermann, P. C., Huber, S. L., Herrler, T., Aicher, A., Ellwart, J. W., Guba, M. O., Bruns, C. J., & Heeschen, C. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.06.002 · Cited by 2,898 · see citing works
EMT Transition States during Tumor Progression and Metastasis
Pastushenko, I., & Blanpain, C. (2018) · Trends in Cell Biology · doi:10.1016/j.tcb.2018.12.001 · Cited by 2,866 · see citing works
Batlle, E., & Clevers, H. (2017) · Nature Medicine · doi:10.1038/nm.4409 · Cited by 2,769 · 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
Puram, S. V., Tirosh, I., Parikh, A. S., Patel, A. P., Yizhak, K., Gillespie, S., Rodman, C., Luo, C. L., Mroz, E. A., Emerick, K. S., et al. (2017) · Cell · doi:10.1016/j.cell.2017.10.044 · Cited by 2,557 · see citing works
Ben‐Porath, I., Thomson, M., Carey, V. J., Ge, R., Bell, G. W., Regev, A., & Weinberg, R. A. (2008) · Nature Genetics · doi:10.1038/ng.127 · Cited by 2,523 · see citing works
Circulating Breast Tumor Cells Exhibit Dynamic Changes in Epithelial and Mesenchymal Composition
Yu, M., Bardia, A., Wittner, B. S., Stott, S. L., Smas, M. E., Ting, D. T., Isakoff, S. J., Ciciliano, J. C., Wells, M. N., Shah, A. M., et al. (2013) · Science · doi:10.1126/science.1228522 · Cited by 2,476 · see citing works
A molecular signature of metastasis in primary solid tumors
Ramaswamy, S., Ross, K. N., Lander, E. S., & Golub, T. R. (2002) · Nature Genetics · doi:10.1038/ng1060 · Cited by 2,448 · see citing works
Circulating Tumor Cell Clusters Are Oligoclonal Precursors of Breast Cancer Metastasis
Aceto, N., Bardia, A., Miyamoto, D. T., Collier, M. D., Wittner, B. S., Spencer, J. A., Yu, M., Pely, A., Engstrom, A., Zhu, H., et al. (2014) · Cell · doi:10.1016/j.cell.2014.07.013 · Cited by 2,438 · see citing works
Breast cancer metastasis: markers and models
Weigelt, B., Peterse, J. L., & van't Veer, L. J. (2005) · Nature Reviews Cancer · doi:10.1038/nrc1670 · Cited by 2,232 · see citing works
Evolution of the Cancer Stem Cell Model
Kreso, A., & Dick, J. E. (2014) · Cell stem cell · doi:10.1016/j.stem.2014.02.006 · Cited by 2,212 · see citing works
Phenotypic characterization of human colorectal cancer stem cells
Dalerba, P. D., Dylla, S. J., Park, I.-K., Liu, R., Wang, X., Cho, R. W., Hoey, T., Gurney, A. L., Huang, E. H., Simeone, D. M., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703478104 · Cited by 2,187 · see citing works
Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation
Malta, T. M., Sokolov, A., Gentles, A. J., Burzykowski, T., Poisson, L., Weinstein, J. N., Kamińska, B., Huelsken, J., Omberg, L., Gevaert, O., et al. (2018) · Cell · doi:10.1016/j.cell.2018.03.034 · Cited by 2,180 · see citing works
A restricted cell population propagates glioblastoma growth after chemotherapy
Chen, J., Li, Y., Yu, T.-S., McKay, R. M., Burns, D. K., Kernie, S. G., & Parada, L. F. (2012) · Nature · doi:10.1038/nature11287 · Cited by 2,096 · see citing works
Zheng, X., Carstens, J. L., Kim, J., Scheible, M., Kaye, J. A., Sugimoto, H., Wu, C.-C., LeBleu, V. S., & Kalluri, R. (2015) · Nature · doi:10.1038/nature16064 · Cited by 2,018 · 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 2,011 · see citing works
The cancer stem cell: premises, promises and challenges
Clevers, H. (2011) · Nature Medicine · doi:10.1038/nm.2304 · Cited by 1,915 · see citing works
Metastasis: a question of life or death
Mehlen, P., & Puisieux, A. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1886 · Cited by 1,854 · see citing works
Recovering Gene Interactions from Single-Cell Data Using Data Diffusion
van Dijk, D., Sharma, R., Nainys, J., Yim, K., Kathail, P., Carr, A. J., Burdziak, C., Moon, K. R., Chaffer, C. L., Pattabiraman, D., et al. (2018) · Cell · doi:10.1016/j.cell.2018.05.061 · Cited by 1,829 · see citing works
Efficient tumour formation by single human melanoma cells
Quintana, E., Shackleton, M. J., Sabel, M. S., Fullen, D. R., Johnson, T. M., & Morrison, S. J. (2008) · Nature · doi:10.1038/nature07567 · Cited by 1,796 · see citing works
Fischer, K. R., Durrans, A., Lee, S., Sheng, J., Li, F., Wong, S. T. C., Choi, H., El Rayes, T., Ryu, S., Troeger, J., et al. (2015) · Nature · doi:10.1038/nature15748 · Cited by 1,791 · see citing works
Identification of the tumour transition states occurring during EMT
Pastushenko, I., Brisebarre, A., Sifrim, A., Fioramonti, M., Revenco, T., Boumahdi, S., Keymeulen, A. V., Brown, D. V., Moers, V., Lemaire, S., et al. (2018) · Nature · doi:10.1038/s41586-018-0040-3 · Cited by 1,488 · see citing works
Stochastic State Transitions Give Rise to Phenotypic Equilibrium in Populations of Cancer Cells
Gupta, P. B., Fillmore, C. M., Jiang, G., Shapira, S. D., Tao, K., Kuperwasser, C., & Lander, E. S. (2011) · Cell · doi:10.1016/j.cell.2011.07.026 · Cited by 1,475 · see citing works
Targeting metastasis-initiating cells through the fatty acid receptor CD36
Pascual, G., Avgustinova, A., Mejetta, S., Martı́n, M., Castellanos‐Martín, A., Attolini, C. S., Berenguer, A., Prats, N., Toll, A., Hueto-Madrid, J. A., et al. (2016) · Nature · doi:10.1038/nature20791 · Cited by 1,430 · see citing works
Metastasis Results from Preexisting Variant Cells Within a Malignant Tumor
Fidler, I. J., & Kripke, M. L. (1977) · Science · doi:10.1126/science.887927 · Cited by 1,426 · see citing works
Identification of cells initiating human melanomas
Schatton, T., Murphy, G. F., Frank, N. Y., Yamaura, K., Waaga-Gasser, A. M., Gasser, M., Zhan, Q., Jordan, S., Duncan, L. M., Weishaupt, C., et al. (2008) · Nature · doi:10.1038/nature06489 · Cited by 1,415 · see citing works
Molecular Definition of Breast Tumor Heterogeneity
Shipitsin, M. V., Campbell, L. L., Argani, P., Weremowicz, S., Bloushtain-Qimron, N., Yao, J., Nikolskaya, T., Serebryiskaya, T., Beroukhim, R., Hu, M., et al. (2007) · Cancer Cell · doi:10.1016/j.ccr.2007.01.013 · Cited by 1,358 · see citing works
Interactions between cancer stem cells and their niche govern metastatic colonization
Malanchi, I., Santamaria-Martínez, A., Susanto, E., Peng, H., Lehr, H.-A., Delaloye, J.-F., & Huelsken, J. (2012) · Nature · doi:10.1038/nature10694 · Cited by 1,339 · see citing works
Cancer stem cells: current status and evolving complexities.
Visvader, J., & Lindeman, G. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.05.007 · Cited by 1,299 · see citing works
Coexistence of Quiescent and Active Adult Stem Cells in Mammals
Li, L., & Clevers, H. (2010) · Science · doi:10.1126/science.1180794 · Cited by 1,247 · see citing works
Multistep Nature of Metastatic Inefficiency
Luzzi, K. J., MacDonald, I. C., Schmidt, E. E., Kerkvliet, N. I., Morris, V. L., Chambers, A. F., & Groom, A. C. (1998) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65628-3 · Cited by 1,246 · see citing works
Charafe-Jauffret, E., Ginestier, C., Iovino, F., Wicinski, J., Cervera, N., Finetti, P., Hur, M., Diebel, M. E., Monville, F., Dutcher, J., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-2741 · Cited by 1,210 · see citing works
Normal and neoplastic nonstem cells can spontaneously convert to a stem-like state
Chaffer, C. L., Brueckmann, I., Scheel, C., Kaestli, A. J., Wiggins, P. A., Rodrigues, L. O., Brooks, M. W., Reinhardt, F., Su, Y., Polyák, K., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102454108 · Cited by 1,137 · see citing works
Senescence-associated reprogramming promotes cancer stemness
Milanovic, M., Fan, D. N. Y., Belenki, D., Däbritz, J. H. M., Zhao, Z., Yu, Y., Dörr, J. R., Dimitrova, L., Lenze, D., Monteiro Barbosa, I. A., et al. (2018) · Nature · doi:10.1038/nature25167 · Cited by 1,131 · see citing works
Tsai, J. H., Donaher, J. L., Murphy, D. A., Chau, S., & Yang, J. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.09.022 · Cited by 1,073 · see citing works
Lineage Tracing Reveals Lgr5 + Stem Cell Activity in Mouse Intestinal Adenomas
Schepers, A. G., Snippert, H. J. G., Stange, D. E., van den Born, M., van Es, J. H., van de Wetering, M., & Clevers, H. C. (2012) · Science · doi:10.1126/science.1224676 · Cited by 1,072 · see citing works
Liu, S., Cong, Y., Wang, D., Sun, Y., Deng, L., Liu, Y., Martin-Trevino, R., Li, S., McDermott, S., Landis, M. D., et al. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2013.11.009 · Cited by 1,056 · see citing works
Baccelli, I., Schneeweiß, A., Riethdorf, S., Stenzinger, A., Schillert, A., Vogel, V., Klein, C., Saini, M., Bäuerle, T., Wallwiener, M., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2576 · Cited by 1,050 · see citing works
Fidler, I. J. (1970) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/45.4.773 · Cited by 1,025 · see citing works
Ocaña, O. H., Córcoles, R. C., Fabra, À., Moreno‐Bueno, G., Acloque, H., Vega, S., Barrallo‐Gimeno, A., Cano, A., & Nieto, M. A. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.10.012 · Cited by 973 · see citing works
Slug and Sox9 Cooperatively Determine the Mammary Stem Cell State
Guo, W., Keckesova, Z., Donaher, J. L., Shibue, T., Tischler, V., Reinhardt, F., Itzkovitz, S., Noske, A., Zürrer‐Härdi, U., Bell, G. W., et al. (2012) · Cell · doi:10.1016/j.cell.2012.02.008 · Cited by 969 · see citing works
Epithelial Plasticity: A Common Theme in Embryonic and Cancer Cells
Nieto, M. A. (2013) · Science · doi:10.1126/science.1234850 · Cited by 962 · see citing works
Merlos-Suárez, A., Barriga, F. M., Jung, P., Iglesias, M., Céspedes, M. V., Rossell, D., Sevillano, M., Hernando-Momblona, X., da Silva-Diz, V., Muñoz, P., et al. (2011) · Cell Stem Cell · doi:10.1016/j.stem.2011.02.020 · Cited by 934 · see citing works
Biological Diversity in Metastatic Neoplasms: Origins and Implications
Fidler, I. J., & Hart, I. R. (1982) · Science · doi:10.1126/science.7112116 · Cited by 926 · see citing works
Single-cell analysis reveals a stem-cell program in human metastatic breast cancer cells
Lawson, D. A., Bhakta, N. R., Kessenbrock, K., Prummel, K. D., Yu, Y., Takai, K., Zhou, A. Y., Eyob, H., Balakrishnan, S., Wang, C., et al. (2015) · Nature · doi:10.1038/nature15260 · Cited by 894 · see citing works
Gene expression profiles of human breast cancer progression
Ma, X., Salunga, R. C., Tuggle, J. T., Gaudet, J., Enright, E., McQuary, P., Payette, T., Pistone, M., Stecker, K., Zhang, B. M., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0931261100 · Cited by 878 · see citing works
Cancer stem cells and epithelial–mesenchymal transition: Concepts and molecular links
Scheel, C., & Weinberg, R. A. (2012) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2012.04.001 · Cited by 872 · see citing works
Cancer Metastasis Is Accelerated through Immunosuppression during Snail-Induced EMT of Cancer Cells
Kudo‐Saito, C., Shirako, H., Takeuchi, T., & Kawakami, Y. (2009) · Cancer Cell · doi:10.1016/j.ccr.2009.01.023 · Cited by 872 · see citing works
Circulating Tumor Cell Clustering Shapes DNA Methylation to Enable Metastasis Seeding
Gkountela, S., Castro-Giner, F., Szczerba, B. M., Vetter, M. H. F., Landin, J., Scherrer, R., Krol, I., Scheidmann, M. C., Beisel, C., Stirnimann, C. U., et al. (2019) · Cell · doi:10.1016/j.cell.2018.11.046 · Cited by 801 · see citing works
Tan, T. Z., Miow, Q. H., Miki, Y., Noda, T., Mori, S., Huang, R. Y., & Thiery, J. P. (2014) · EMBO Molecular Medicine · doi:10.15252/emmm.201404208 · Cited by 792 · see citing works
Metastatic Latency and Immune Evasion through Autocrine Inhibition of WNT
Malladi, S., Macalinao, D. G., Jin, X., He, L., Basnet, H., Zou, Y., de Stanchina, E., & Massagué, J. (2016) · Cell · doi:10.1016/j.cell.2016.02.025 · Cited by 791 · see citing works
A distinct role for Lgr5+ stem cells in primary and metastatic colon cancer
Melo, F. D. S. E., Kurtova, A. V., Harnoss, J. M., Kljavin, N. M., Hoeck, J. D., Hung, J., Anderson, J. E., Storm, E. E., Modrusan, Z. D., Koeppen, H., et al. (2017) · Nature · doi:10.1038/nature21713 · Cited by 782 · see citing works
MULTIPOTENTIALITY OF SINGLE EMBRYONAL CARCINOMA CELLS.
Kleinsmith, L. J., & Pierce, G. B. (1964) · PubMed · Cited by 771 · see citing works
Cancer stem cells: The challenges ahead
Medema, J. P. (2013) · Nature Cell Biology · doi:10.1038/ncb2717 · Cited by 740 · see citing works
Cheung, K. J., Padmanaban, V., Silvestri, V. L., Schipper, K., Cohen, J. D., Fairchild, A. N., Gorin, M. A., Verdone, J. E., Pienta, K. J., Bader, J. S., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508541113 · Cited by 737 · see citing works
Charafe-Jauffret, E., Ginestier, C., Iovino, F., Tarpin, C., Diebel, M., Esterni, B., Houvenaeghel, G., Extra, J.-M., Bertucci, F., Jacquemier, J., et al. (2010) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-09-1630 · Cited by 732 · see citing works
Defining the mode of tumour growth by clonal analysis
Driessens, G., Beck, B., Caauwe, A., Simons, B. D., & Blanpain, C. (2012) · Nature · doi:10.1038/nature11344 · Cited by 718 · see citing works
A microfluidic device for label-free, physical capture of circulating tumor cell clusters
Sarioglu, A. F., Aceto, N., Kojić, N., Collier, M. D., Zeinali, M., Hamza, B. M., Engstrom, A., Zhu, H., Sundaresan, T. K., Miyamoto, D. T., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3404 · Cited by 715 · see citing works
EMT Subtype Influences Epithelial Plasticity and Mode of Cell Migration
Aiello, N. M., Maddipati, R., Norgard, R. J., Balli, D., Li, J., Yuan, S., Yamazoe, T., Black, T. A., Sahmoud, A., Furth, E. E., et al. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.05.027 · Cited by 708 · 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
Distinct EMT programs control normal mammary stem cells and tumour-initiating cells
Ye, X., Tam, W. L., Shibue, T., Kaygusuz, Y., Reinhardt, F., Eaton, E. N., & Weinberg, R. A. (2015) · Nature · doi:10.1038/nature14897 · Cited by 697 · see citing works
Single-cell dissection of transcriptional heterogeneity in human colon tumors
Dalerba, P. D., Tomer Kalisky, C., Sahoo, D., Rajendran, P. S., Rothenberg, M. E., Leyrat, A. A., Sim, S., Okamoto, J., Johnston, D. M., Qian, D., et al. (2011) · Nature Biotechnology · doi:10.1038/nbt.2038 · Cited by 693 · see citing works
Implications of the Hybrid Epithelial/Mesenchymal Phenotype in Metastasis
Jolly, M. K. (2015) · Frontiers in Oncology · doi:10.3389/fonc.2015.00155 · Cited by 684 · see citing works
Self-citationArmstrong, A. J., Marengo, M. S., Oltean, S., Kemeny, G., Bitting, R. L., Turnbull, J. D., Herold, C. I., Marcom, P. K., George, D. J., & García-Blanco, M. A. (2011) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-10-0490 · Cited by 646 · see citing works
Tumour heterogeneity and metastasis at single-cell resolution
Lawson, D. A., Kessenbrock, K., Davis, R. T., Pervolarakis, N., & Werb, Z. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0236-7 · Cited by 606 · see citing works
Quintana, E., Shackleton, M. J., Foster, H. R., Fullen, D. R., Sabel, M. S., Johnson, T. M., & Morrison, S. J. (2010) · Cancer Cell · doi:10.1016/j.ccr.2010.10.012 · Cited by 599 · see citing works
Phenotypic Plasticity: Driver of Cancer Initiation, Progression, and Therapy Resistance
Gupta, P. B., Pastushenko, I., Skibinski, A., Blanpain, C., & Kuperwasser, C. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.11.011 · Cited by 596 · see citing works
A Subpopulation of CD26+ Cancer Stem Cells with Metastatic Capacity in Human Colorectal Cancer
Pang, R. W. C., Law, W. L., Chu, A. C. Y., Poon, J. T. C., Lam, C. S. C., Chow, A. K.-M., Ng, L., Cheung, L. W., Lan, X. R., Lan, H. Y., et al. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.04.001 · Cited by 540 · see citing works
Tumor Budding: The Name is EMT. Partial EMT.
Grigore, A. D., Jolly, M. K., Jia, D., Farach‐Carson, M. C., & Levine, H. (2016) · Journal of Clinical Medicine · doi:10.3390/jcm5050051 · Cited by 493 · see citing works
Self-citationAcquisition of a hybrid E/M state is essential for tumorigenicity of basal breast cancer cells
Kröger, C., Afeyan, A. B., Mraz, J., Eaton, E. N., Reinhardt, F., Khodor, Y. L., Thiru, P., Bierie, B., Ye, X., Burge, C. B., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1812876116 · Cited by 493 · see citing works
MicroRNA-based regulation of epithelial–hybrid–mesenchymal fate determination
Lu, M., Jolly, M. K., Levine, H., Onuchic, J. N., & Ben‐Jacob, E. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1318192110 · Cited by 481 · see citing works
Self-citationLiu, H., Patel, M. R., Prescher, J. A., Patsialou, A., Qian, D., Lin, J., Wen, S., Chang, Y.-F., Bachmann, M. H., Shimono, Y., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006732107 · Cited by 465 · see citing works
Celià-Terrassa, T., Meca‐Cortés, Ó., Mateo, F., de Paz, A. M., Rubio, N., Estape, A. A., Ell, B. J., Bermudo, R., Díaz, A., Guerra‐Rebollo, M., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci59218 · Cited by 448 · see citing works
Self-citationGene expression profiles of primary breast tumors maintained in distant metastases
Weigelt, B., Glas, A. M., Wessels, L. F. A., Witteveen, A. T., Peterse, J. L., & Veer, L. J. V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2634067100 · Cited by 431 · see citing works
Stability of the hybrid epithelial/mesenchymal phenotype
Jolly, M. K., Tripathi, S. C., Jia, D., Mooney, S. M., Çeliktaş, M., Hanash, S., Mani, S. A., Pienta, K. J., Ben‐Jacob, E., & Levine, H. (2016) · Oncotarget · doi:10.18632/oncotarget.8166 · Cited by 427 · see citing works
Self-citationNew insights into the role of <scp>EMT</scp> in tumor immune escape
Terry, S., Savagner, P., Ortiz‐Cuaran, S., Mahjoubi, L., Saintigny, P., Thiery, J., & Chouaib, S. (2017) · Molecular Oncology · doi:10.1002/1878-0261.12093 · Cited by 414 · see citing works
Cameron, M. D., Schmidt, E. E., Kerkvliet, N. I., Nadkarni, K. V., Morris, V. L., Groom, A. C., Chambers, A. F., & MacDonald, I. C. (2000) · PubMed · Cited by 400 · see citing works
A Quantitative Assay for the Number of Murine Lymphoma Cells capable of Proliferation in vivo
Bruce, W. R., & van der Gaag, H. (1963) · Nature · doi:10.1038/199079a0 · Cited by 399 · see citing works
EMT and MET : necessary or permissive for metastasis?
Jolly, M. K., Ware, K. E., Gilja, S., Somarelli, J. A., & Levine, H. (2017) · Molecular Oncology · doi:10.1002/1878-0261.12083 · Cited by 371 · see citing works
Self-citationGroße-Wilde, A., d’Hérouël, A. F., McIntosh, E., Ertaylan, G., Skupin, A., Kuestner, R. E., del Sol, A., Walters, K., & Huang, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0126522 · Cited by 367 · see citing works
Pierce, G. B., & Speers, W. C. (1988) · PubMed · Cited by 365 · see citing works
Single‐cell analysis reveals cancer stem cell heterogeneity in hepatocellular carcinoma
Zheng, H., Pomyen, Y., Hernandez, M. O., Li, C., Livák, F., Tang, W., Dang, H. T., Greten, T. F., Davis, J. L., Zhao, Y., et al. (2018) · Hepatology · doi:10.1002/hep.29778 · Cited by 350 · see citing works
Distinctive properties of metastasis-initiating cellsPreprint
Celià-Terrassa, T., & Kang, Y. (2016) · Genes & Development · doi:10.1101/gad.277681.116 · Cited by 333 · see citing works
Self-citationHybrid epithelial/mesenchymal phenotypes promote metastasis and therapy resistance across carcinomas
Jolly, M. K., Somarelli, J. A., Sheth, M. U., Biddle, A., Tripathi, S. C., Armstrong, A. J., Hanash, S., Bapat, S. A., Rangarajan, A., & Levine, H. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.09.007 · Cited by 327 · see citing works
Self-citationToward understanding cancer stem cell heterogeneity in the tumor microenvironment
Bocci, F., Gearhart-Serna, L., Boareto, M., Ribeiro, M. P. C., Ben‐Jacob, E., Devi, G. R., Levine, H., Onuchic, J. N., & Jolly, M. K. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1815345116 · Cited by 300 · see citing works
Self-citationDistinct types of tumor-initiating cells form human colon cancer tumors and metastases
Dieter, S. M., Ball, C. R., Hoffmann, C. M., Nowrouzi, A., Herbst, F., Zavidij, O., Abel, U., Arens, A., Weichert, W., Brand, K., et al. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.08.010 · Cited by 297 · see citing works
The Transmission of Leukemia of Mice with a Single Cell
Fürth, J., Kahn, M. C., & Breedis, C. (1937) · American Journal of Cancer · doi:10.1158/ajc.1937.276 · Cited by 271 · see citing works
Goldman, A., Majumder, B., Dhawan, A., Ravi, S., Goldman, D., Kohandel, M., Majumder, P. K., & Sengupta, S. (2015) · Nature Communications · doi:10.1038/ncomms7139 · Cited by 260 · see citing works
Esposito, M., Mondal, N., Greco, T. M., Wei, Y., Spadazzi, C., Lin, S.-C., Zheng, H., Cheung, C., Magnani, J. L., Lin, S.-H., et al. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0309-2 · Cited by 250 · see citing works
Survival Outcomes in Cancer Patients Predicted by a Partial EMT Gene Expression Scoring Metric
George, J. T., Jolly, M. K., Xu, S., Somarelli, J. A., & Levine, H. (2017) · Cancer Research · doi:10.1158/0008-5472.can-16-3521 · Cited by 245 · see citing works
Self-citationTsuji, T., Ibaragi, S., Shima, K., Hu, M. G., Katsurano, M., Sasaki, A., & Hu, G.-F. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-1444 · Cited by 236 · see citing works
Karacosta, L. G., Anchang, B., Ignatiadis, N., Kimmey, S. C., Benson, J. A., Shrager, J. B., Tibshirani, R. J., Bendall, S. C., & Plevritis, S. K. (2019) · Nature Communications · doi:10.1038/s41467-019-13441-6 · Cited by 211 · see citing works
Cell plasticity in epithelial homeostasis and tumorigenesis
Varga, J., & Greten, F. R. (2017) · Nature Cell Biology · doi:10.1038/ncb3611 · Cited by 204 · see citing works
Implications of the hybrid epithelial/mesenchymal phenotype in metastasisPreprint
Jolly, M. K., Boareto, M., Huang, B., et al. (2015) · arXiv (Cornell University) · doi:10.48550/arxiv.1505.07494 · Cited by 204 · see citing works
Self-citationTripathi, S. C., Peters, H. L., Taguchi, A., Katayama, H., Wang, H., Momin, A. A., Jolly, M. K., Çeliktaş, M., Rodriguez‐Canales, J., Liu, H., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1521812113 · Cited by 203 · see citing works
Self-citationHeterogeneous Tumor Subpopulations Cooperate to Drive Invasion
Chapman, A., del Ama, L. F., Ferguson, J., Kamarashev, J. A., Wellbrock, C., & Hurlstone, A. F. L. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.045 · Cited by 195 · see citing works
Strauss, R., Li, Z., Liu, Y., Beyer, I., Persson, J., Sova, P., Möller, T., Pesonen, S. A., Hemminki, A., Hamerlik, P., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016186 · Cited by 194 · see citing works
An epigenetically distinct breast cancer cell subpopulation promotes collective invasion
Westcott, J. M., Prechtl, A. M., Maine, E. A., Dang, T. T., Esparza, M. A., Sun, H., Zhou, Y., Xie, Y., & Pearson, G. W. (2015) · Journal of Clinical Investigation · doi:10.1172/jci77767 · Cited by 179 · see citing works
Metastatic niche functions and therapeutic opportunities
Celià-Terrassa, T., & Kang, Y. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0145-9 · Cited by 172 · see citing works
Self-citationCoupling the modules of EMT and stemness: A tunable ‘stemness window’ model
Jolly, M. K., Jia, D., Boareto, M., Mani, S. A., Pienta, K. J., Ben‐Jacob, E., & Levine, H. (2015) · Oncotarget · doi:10.18632/oncotarget.4629 · Cited by 171 · see citing works
Self-citationGiraddi, R. R., Chung, C., Heinz, R. E., Balcioglu, O., Novotny, M. A., Trejo, C. L., Dravis, C., Hagos, B. M., Mehrabad, E. M., Rodewald, L. W., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.025 · Cited by 166 · see citing works
CD133+CXCR4+ colon cancer cells exhibit metastatic potential and predict poor prognosis of patients
Zhang, S., Han, Z., Jing, Y.-Y., Tao, S., Li, T., Wang, H., Wang, Y., Li, R., Yang, Y., Zhao, X., et al. (2012) · BMC Medicine · doi:10.1186/1741-7015-10-85 · Cited by 164 · see citing works
Celià-Terrassa, T., Bastian, C. D., Liu, D. D., Ell, B. J., Aiello, N. M., Wei, Y., Zamalloa, J., Blanco, M. A., Hang, X., Kunisky, D., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07538-7 · Cited by 163 · see citing works
Self-citationFURTHER EVIDENCE FAVORING THE CONCEPT OF THE STEM CELL IN ASCITES TUMORS OF RATS
Makino, S. (1956) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1956.tb50894.x · Cited by 151 · see citing works
Brief Report: Intravital Imaging of Cancer Stem Cell Plasticity in Mammary Tumors
Zomer, A., Ellenbroek, S. I. J., Ritsma, L., Beerling, E., Vrisekoop, N., & van Rheenen, J. (2012) · Stem Cells · doi:10.1002/stem.1296 · Cited by 151 · see citing works
Aldehyde dehydrogenase as a marker and functional mediator of metastasis in solid tumors
Rodriguez-Torres, M., & Allan, A. L. (2015) · Clinical & Experimental Metastasis · doi:10.1007/s10585-015-9755-9 · Cited by 148 · see citing works
Quantitative studies of autotransplantation of human cancer.Preliminary report
Southam, C. M., & Brunschwig, A. (1961) · Cancer · doi:10.1002/1097-0142(196109/10)14:5 · Cited by 145 · see citing works
Merino, D., Weber, T. S., Serrano, A., Vaillant, F., Liu, K., Pal, B., Di Stefano, L., Schreuder, J., Lin, D., Chen, Y., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08595-2 · Cited by 145 · see citing works
Heterogeneity of Human Breast Stem and Progenitor Cells as Revealed by Transcriptional Profiling
Colacino, J. A., Azizi, E., Brooks, M. D., Harouaka, R. A., Fouladdel, S., McDermott, S., Lee, M., Hill, D. R., Madden, J. M., Boerner, J. L., et al. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.03.001 · Cited by 140 · see citing works
Bocci, F., Tripathi, S. C., Mercedes, S. A. V., George, J. T., Casabar, J. P., Wong, P. K., Hanash, S., Levine, H., Onuchic, J. N., & Jolly, M. K. (2019) · Integrative Biology · doi:10.1093/intbio/zyz021 · Cited by 132 · see citing works
Self-citationMultistable Decision Switches for Flexible Control of Epigenetic Differentiation
Guantes, R., & Poyatos, J. F. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000235 · Cited by 125 · see citing works
Boareto, M., Jolly, M. K., Goldman, A. J., Pietilä, M., Mani, S. A., Sengupta, S., Ben‐Jacob, E., Levine, H., & Onuchic, J. N. (2016) · Journal of The Royal Society Interface · doi:10.1098/rsif.2015.1106 · Cited by 119 · see citing works
Self-citationJagged mediates differences in normal and tumor angiogenesis by affecting tip-stalk fate decision
Boareto, M., Jolly, M. K., Ben‐Jacob, E., & Onuchic, J. N. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1511814112 · Cited by 116 · see citing works
Self-citationA mechanism for epithelial-mesenchymal heterogeneity in a population of cancer cells
Tripathi, S., Chakraborty, P., Levine, H., & Jolly, M. K. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007619 · Cited by 112 · see citing works
Self-citationAndriani, F., Bertolini, G., Facchinetti, F., Baldoli, E., Moro, M., Casalini, P., Caserini, R., Milione, M., Leone, G., Pelosi, G., et al. (2015) · Molecular Oncology · doi:10.1016/j.molonc.2015.10.002 · Cited by 111 · see citing works
Cell-State Transitions Regulated by SLUG Are Critical for Tissue Regeneration and Tumor Initiation
Phillips, S. M., Prat, A., Sedic, M., Proia, T. A., Wronski, A., Mazumdar, S., Skibinski, A., Shirley, S. H., Perou, C. M., Gill, G., et al. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.03.008 · Cited by 108 · see citing works
Reeves, M. Q., Kandyba, E. E., Harris, S., Rosario, R. D., & Balmain, A. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0109-0 · Cited by 105 · see citing works
Celià-Terrassa, T., Liu, D. D., Choudhury, A., Hang, X., Wei, Y., Zamalloa, J., Alfaro‐Aco, R., Chakrabarti, R., Jiang, Y., Koh, B. I., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3533 · Cited by 103 · see citing works
Self-citationStylianou, N., Lehman, M., Wang, C., Fard, A. T., Rockstroh, A., Fazli, L., Jovanovic, L., Ward, M. S., Sadowski, M. C., Kashyap, A. S., et al. (2018) · Oncogene · doi:10.1038/s41388-018-0488-5 · Cited by 101 · see citing works
Chen, K., Pan, F., Jiang, H., Chen, J., Li, P. Z., Xie, F., & Liang, H. (2011) · Clinical & Experimental Metastasis · doi:10.1007/s10585-011-9407-7 · Cited by 99 · see citing works
Phenotypic Plasticity and Cell Fate Decisions in Cancer: Insights from Dynamical Systems Theory
Jia, D., Jolly, M. K., Kulkarni, P., & Levine, H. (2017) · Cancers · doi:10.3390/cancers9070070 · Cited by 94 · see citing works
Self-citationReuben, J. M., Lee, B.-N., Gao, H., Cohen, E. N., Mego, M., Giordano, A., Wang, X., Lodhi, A., Krishnamurthy, S., Hortobágyi, G. N., et al. (2011) · European Journal of Cancer · doi:10.1016/j.ejca.2011.01.011 · Cited by 92 · see citing works
Metastatic Potential of Cancer Stem Cells in Head and Neck Squamous Cell Carcinoma
Davis, S. J., Divi, V., Owen, J. H. J., Bradford, C. R., Carey, T. E., Papagerakis, S. M., & Prince, M. E. (2010) · Archives of Otolaryngology - Head and Neck Surgery · doi:10.1001/archoto.2010.219 · Cited by 92 · see citing works
Chebouti, I., Kasimir‐Bauer, S., Buderath, P., Wimberger, P., Hauch, S., Kimmig, R., & Kuhlmann, J. D. (2017) · Oncotarget · doi:10.18632/oncotarget.16179 · Cited by 92 · see citing works
Ambiguous cells: the emergence of the stem cell concept in the nineteenth and twentieth centuries
Maehle, A. (2011) · Notes and Records the Royal Society Journal of the History of Science · doi:10.1098/rsnr.2011.0023 · Cited by 85 · see citing works
A Hierarchical Regulatory Landscape during the Multiple Stages of EMT
Meyer‐Schaller, N., Cardner, M., Diepenbruck, M., Saxena, M. T., Tiede, S., Lüönd, F., Ivánek, R., Beerenwinkel, N., & Christofori, G. (2019) · Developmental Cell · doi:10.1016/j.devcel.2018.12.023 · Cited by 84 · see citing works
Selective depletion of metastatic stem cells as therapy for human colorectal cancer
Céspedes, M. V., Unzueta, U., Aviñó, A. M., Gallardo, A., Álamo, P., Sala, R., Sánchez‐Chardi, A., Casanova, I., Mangues, M. A., Pousa, A. L., et al. (2018) · EMBO Molecular Medicine · doi:10.15252/emmm.201708772 · Cited by 80 · see citing works
Evolution and Phenotypic Selection of Cancer Stem Cells
Poleszczuk, J., Hahnfeldt, P., & Enderling, H. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004025 · Cited by 76 · see citing works
Bocci, F., Jolly, M. K., George, J. T., Levine, H., & Onuchic, J. N. (2018) · Oncotarget · doi:10.18632/oncotarget.25692 · Cited by 67 · see citing works
Self-citationJolly, M. K., Tripathi, S. C., Somarelli, J. A., Hanash, S., & Levine, H. (2017) · Molecular Oncology · doi:10.1002/1878-0261.12084 · Cited by 65 · see citing works
Self-citationCharacterizing heterogeneity in leukemic cells using single-cell gene expression analysis
Saadatpour, A., Guo, G., Orkin, S., & Yuan, G.-C. (2014) · Genome Biology · doi:10.1186/s13059-014-0525-9 · Cited by 62 · see citing works
Markiewicz, A., Topa, J., Nagel, A. C., Skokowski, J., Seroczyńska, B., Stokowy, T., Wełnicka-Jaśkiewicz, M., & Zaczek, A. J. (2019) · Cancers · doi:10.3390/cancers11010059 · Cited by 55 · see citing works
A Biophysical Model Uncovers the Size Distribution of Migrating Cell Clusters across Cancer Types
Bocci, F., Jolly, M. K., & Onuchic, J. N. (2019) · Cancer Research · doi:10.1158/0008-5472.can-19-1726 · Cited by 45 · see citing works
Self-citationActivity‐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
Jolly, M. K., Ware, K. E., Xu, S., Gilja, S., Shetler, S., Yang, Y., Wang, X., Austin, R. G., Runyambo, D., Hish, A. J., et al. (2019) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-18-0763 · Cited by 39 · see citing works
Self-citationAssociation of stem cell marker CD133 expression with dissemination of glioblastomas
for the Tohoku Brain Tumor Study Group, Satō, A., Sakurada, K., Kumabe, T., Sasajima, T., Beppu, T., Asano, K., Ohkuma, H., Ogawa, A., Mizoi, K., et al. (2010) · Neurosurgical Review · doi:10.1007/s10143-010-0239-8 · Cited by 32 · see citing works
Computational systems biology of epithelial-hybrid-mesenchymal transitions
Jolly, M. K., & Levine, H. (2017) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2017.02.004 · Cited by 25 · see citing works
Self-citationLearning time-varying information flow from single-cell epithelial to mesenchymal transition data
Krishnaswamy, S., Zivanovic, N., Sharma, R., Pe’er, D., & Bodenmiller, B. (2018) · PLoS ONE · doi:10.1371/journal.pone.0203389 · Cited by 24 · see citing works
Bocci, F., Jolly, M. K., & Onuchic, J. N. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/563049 · Cited by 7 · see citing works
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TGFβ biology in cancer progression and immunotherapy
Derynck, R., Turley, S. J., & Akhurst, R. J. (2021) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-020-0403-1 · Cited by 944 · 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
Bhat, G. R., Sethi, I., Sadida, H. Q., Rah, B., Mir, R., Algehainy, N. A., Albalawi, I. A., Masoodi, T., Subbaraj, G. K., Jamal, F., et al. (2024) · Cancer and Metastasis Reviews · doi:10.1007/s10555-024-10172-z · Cited by 313 · see citing works
Do, H. T. T., Lee, C. H., & Cho, J. (2020) · Cancers · doi:10.3390/cancers12020287 · Cited by 236 · see citing works
Cancer Stem Cell Plasticity – A Deadly Deal
Thankamony, A. P., Saxena, K., Murali, R., Jolly, M. K., & Nair, R. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00079 · Cited by 173 · see citing works
Self-citationChen, X., Yang, M., Yin, J., Li, P., Zeng, S., Zheng, G., He, Z., Liu, H., Wang, Q., Zhang, F., et al. (2022) · Cell Communication and Signaling · doi:10.1186/s12964-022-00888-2 · Cited by 165 · see citing works
Interferons in cancer immunoediting: sculpting metastasis and immunotherapy response
von Locquenghien, M., Rozalén, C., & Celià-Terrassa, T. (2021) · Journal of Clinical Investigation · doi:10.1172/jci143296 · Cited by 144 · see citing works
Self-citationNimmakayala, R. K., Leon, F., Rachagani, S., Rauth, S., Nallasamy, P., Marimuthu, S., Shailendra, G. K., Chhonker, Y. S., Chugh, S., Chirravuri, R., et al. (2020) · Oncogene · doi:10.1038/s41388-020-01518-2 · Cited by 142 · see citing works
Sun, Z., Zhao, Y., Yan, W., Ding, X., Tan, C., & Wang, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.939523 · Cited by 104 · see citing works
Cancer Stem Cells as a Potential Target to Overcome Multidrug Resistance
Cho, Y., & Kim, Y. K. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00764 · Cited by 103 · see citing works
Emerging Role of E2F Family in Cancer Stem Cells
Xie, D., Qin, P., Li, J., Wan, X., & Ye, T. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.723137 · Cited by 94 · see citing works
Signaling pathways in the regulation of cancer stem cells and associated targeted therapy
Wang, M., & Wu, M. (2022) · MedComm · doi:10.1002/mco2.176 · Cited by 92 · see citing works
Cancer-associated fibroblasts in non-small cell lung cancer: Recent advances and future perspectives
Zhang, H., Jiang, H., Zhu, L., Li, J., & Ma, S. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.05.009 · Cited by 85 · see citing works
El‐Tanani, M., Rabbani, S. A., Satyam, S. M., Rangraze, I. R., Wali, A. F., El‐Tanani, Y., & Aljabali, A. A. A. (2025) · Cancers · doi:10.3390/cancers17030382 · Cited by 67 · see citing works
Zheng, X., Yu, C., & Xu, M. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.678333 · Cited by 59 · see citing works
Chemokines orchestrate tumor cells and the microenvironment to achieve metastatic heterogeneity
Saxena, S., & Singh, R. K. (2021) · Cancer and Metastasis Reviews · doi:10.1007/s10555-021-09970-6 · Cited by 53 · see citing works
Hass, R., von der Ohe, J., & Ungefroren, H. (2020) · Cancers · doi:10.3390/cancers12123674 · Cited by 53 · see citing works
The Roles of Stroma-Derived Chemokine in Different Stages of Cancer Metastases
Hussain, S., Peng, B., Cherian, M. A., Song, J. W., Ahirwar, D. K., & Ganju, R. K. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.598532 · Cited by 49 · see citing works
Tangsiri, M., Hheidari, A., Liaghat, M., Razlansari, M., Ebrahimi, N., Akbari, A., Varnosfaderani, S. M. N., Maleki‐Sheikhabadi, F., Norouzi, A., Bakhtiyari, M., et al. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115973 · Cited by 54 · see citing works
Hybrid E/M Phenotype(s) and Stemness: A Mechanistic Connection Embedded in Network Topology
Pasani, S., Sahoo, S., & Jolly, M. K. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm10010060 · Cited by 46 · see citing works
Self-citationMarkers and Reporters to Reveal the Hierarchy in Heterogeneous Cancer Stem Cells
Mohan, A., Rajan, R. R., Mohan, G., Puthenveettil, P. K., & Maliekal, T. T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.668851 · Cited by 45 · see citing works
Zhu, M., Fan, H., Deng, J., Jiang, K., Liao, J., Xiao-yue, Z., Chen, Y., Yu, M., & Peng, Z. (2023) · ACS Nano · doi:10.1021/acsnano.3c04636 · Cited by 44 · see citing works
Monteleone, L., Speciale, A., Valenti, G. E., Traverso, N., Ravera, S., Garbarino, O., Leardi, R., Farinini, E., Roveri, A., Ursini, F., et al. (2021) · Antioxidants · doi:10.3390/antiox10050691 · Cited by 44 · see citing works
Zhao, X., Shu, D., Sun, W., Si, S., Ran, W., Guo, B., & Cui, L. (2022) · 癌症:英文版 · doi:10.1002/cac2.12349 · Cited by 40 · see citing works
Tumor Hybrid Cells: Nature and Biological Significance
Tretyakova, M. S., Subbalakshmi, A. R., Menyailo, M. E., Jolly, M. K., & Denisov, E. V. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.814714 · Cited by 39 · see citing works
Self-citationSubbalakshmi, A. R., Sahoo, S., McMullen, I., Saxena, A. N., Venugopal, S., Somarelli, J. A., & Jolly, M. K. (2021) · Cancers · doi:10.3390/cancers13205135 · Cited by 38 · see citing works
Self-citationProgress of tumor-associated macrophages in the epithelial-mesenchymal transition of tumor
Li, X., Chen, L., Peng, X., & Zhan, X. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.911410 · Cited by 37 · see citing works
Gašparović, A. Č., Milković, L., Dandachi, N., Stanzer, S., Pezdirc, I., Vrančić, J., Šitić, S., Suppan, C., & Balić, M. (2019) · Antioxidants · doi:10.3390/antiox8120633 · Cited by 36 · see citing works
Circulating tumor cell-derived preclinical models: current status and future perspectives
Kahounová, Z., Pícková, M., Drápela, S., Bouchal, J., Szczyrbová, E., Navrátil, J., & Souček, K. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06059-6 · Cited by 37 · see citing works
Antimetastatic defense by CD8+ T cells
de Lara, P. T., Castañón, H., Sterpi, M., & van den Broek, M. F. (2021) · Trends in cancer · doi:10.1016/j.trecan.2021.10.006 · Cited by 32 · see citing works
Regulation of epithelial-mesenchymal transition by protein lysine acetylation
Kong, F., Ma, L., Wang, X., You, H., Zheng, K., & Tang, R. (2022) · Cell Communication and Signaling · doi:10.1186/s12964-022-00870-y · Cited by 32 · see citing works
Zang, W., Geng, F., Liu, J., Wang, Z., Zhang, S., Li, Y., Lu, Z., & Pan, Y. (2025) · International Journal of Oral Science · doi:10.1038/s41368-024-00342-8 · Cited by 29 · see citing works
Nanotechnology‐Based Strategies to Evaluate and Counteract Cancer Metastasis and Neoangiogenesis
Şen, Ö., Emanet, M., & Ciofani, G. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202002163 · Cited by 29 · see citing works
Fridrichová, I., Kalinkova, L., & Čierniková, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012141 · Cited by 29 · see citing works
Reporters of Cancer Stem Cells as a Tool for Drug Discovery
Mohan, A., Reshma Raj, R., Mohan, G., Padmaja, K. P., & Maliekal, T. T. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.669250 · Cited by 28 · see citing works
Regulatory roles of RNA modifications in breast cancer
Kumari, K., Groza, P., & Aguiló, F. (2021) · NAR Cancer · doi:10.1093/narcan/zcab036 · Cited by 28 · see citing works
Muralidharan, S., Sahoo, S., Saha, A., Chandran, S., Majumdar, S. S., Mandal, S., Levine, H., & Jolly, M. K. (2022) · Biomolecules · doi:10.3390/biom12020297 · Cited by 28 · see citing works
Self-citationDeregulated E2F Activity as a Cancer-Cell Specific Therapeutic Tool
Nakajima, R., Zhao, L., Zhou, Y., Shirasawa, M., Uchida, A., Murakawa, H., Fikriyanti, M., Iwanaga, R., Bradford, A. P., Araki, K., et al. (2023) · Genes · doi:10.3390/genes14020393 · Cited by 30 · see citing works
Lei, Y., Wang, X., Sun, H., Fu, Y., Tian, Y., Yang, L., Wang, J., & Xia, F. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.601668 · Cited by 25 · see citing works
Yang, D., Ma, Y., Zhao, P., Ma, J., & He, C. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112860 · Cited by 25 · see citing works
Prognostic Role of Immune Checkpoint Regulators in Cholangiocarcinoma: A Pilot Study
Cao, L., Prithviraj, P., Shrestha, R., Sharma, R., Anaka, M., Bridle, K. R., Kannourakis, G., Crawford, D. H., & Jayachandran, A. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10102191 · Cited by 24 · see citing works
Dual cancer stem cell manipulation to enhance phototherapy against tumor progression and metastasis
Shang, Q., Zhou, S., Zhou, Z., Jiang, Y., & Luan, Y. (2021) · Journal of Controlled Release · doi:10.1016/j.jconrel.2021.10.029 · Cited by 25 · see citing works
TGFβ family signaling in human stem cell self-renewal and differentiation
Liu, S., Ren, J., Hu, Y., Zhou, F., & Zhang, L. (2024) · Cell Regeneration · doi:10.1186/s13619-024-00207-9 · Cited by 23 · see citing works
Sahoo, S., Ashraf, B., Duddu, A. S., Biddle, A., & Jolly, M. K. (2022) · Clinical & Experimental Metastasis · doi:10.1007/s10585-021-10139-2 · Cited by 23 · see citing works
Self-citationAcuña, R. A., Varas‐Godoy, M., Herrera-Sepulveda, D., & Retamal, M. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212604 · Cited by 23 · see citing works
Berrino, C., & Omar, A. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46060323 · Cited by 22 · see citing works
Yadav, P., Rajendrasozhan, S., Lajimi, R. H., Patel, R. R., Heymann, D., & Prasad, N. R. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1494723 · Cited by 23 · see citing works
Mitochondria in oral cancer stem cells: Unraveling the potential drug targets for new and old drugs
Olmedo, I., Martínez, D., Carrasco-Rojas, J., & Jara, J. A. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122065 · Cited by 21 · see citing works
Wei, B., Cao, J., Tian, J., Yu, C.-Y., Huang, Q., Yu, J., Ma, R., Wang, J., Xu, F., & Wang, L. (2021) · PubMed Central · Cited by 20 · see citing works
Bocci, F., Zhou, P., & Nie, Q. H. (2021) · Cancers · doi:10.3390/cancers13225726 · Cited by 20 · see citing works
Zhao, Q. S., Long, Y., Cheng, W., Huang, Y., Li, J., Li, Y., Li, X., Guo, X., Li, Y., Li, G., et al. (2022) · International Journal of Oncology · doi:10.3892/ijo.2022.5365 · Cited by 19 · see citing works
DDX56 promotes EMT and cancer stemness via MELK-FOXM1 axis in hepatocellular carcinoma
Li, Q., Wang, T., Wang, X., Ge, X., Yang, T., & Wang, W. (2024) · iScience · doi:10.1016/j.isci.2024.109827 · Cited by 18 · see citing works
Wang, X., Li, H., Ran, X., Li, X., Zhang, X., Jin, T., & Zhang, H. (2023) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-023-04777-1 · Cited by 17 · see citing works
Integrins as Key Mediators of Metastasis
Cáceres-Calle, D., Torre-Cea, I., Marcos-Zazo, L., Carrera-Aguado, I., Guerra-Paes, E., Berlana-Galán, P., Muñoz‐Félix, J. M., & Sánchez‐Juanes, F. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26030904 · Cited by 19 · see citing works
Chemokines network in bone metastasis: Vital regulators of seeding and soiling
Sharma, G., Pothuraju, R., Kanchan, R. K., Batra, S. K., & Siddiqui, J. A. (2022) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2022.02.003 · Cited by 17 · see citing works
Proteases Regulate Cancer Stem Cell Properties and Remodel Their Microenvironment
Habič, A., Novak, M., Majc, B., Turnšek, T. L., & Breznik, B. (2021) · Journal of Histochemistry & Cytochemistry · doi:10.1369/00221554211035192 · Cited by 16 · see citing works
Intermittent Hypoxia Mediates Paraspeckle Protein-1 Upregulation in Sleep Apnea
Díaz‐García, E., García-Tovar, S., Casitas, R., Oriol, A. J., Zamarrón, E., Sánchez-Sánchez, B., Sastre-Perona, A., López‐Collazo, E., Rio, F. G., & Cubillos‐Zapata, C. (2021) · Cancers · doi:10.3390/cancers13153888 · Cited by 17 · see citing works
Polak, K. L., Tamagno, I., Parameswaran, N., Smigiel, J. M., Chan, E. R., Yuan, X., Rios, B. L., & Jackson, M. W. (2023) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-22-0715 · Cited by 17 · see citing works
Small cell lung cancer with liver metastases: from underlying mechanisms to treatment strategies
Fan, L., Lin, Y., Fu, Y., & Wang, J. (2024) · Cancer and Metastasis Reviews · doi:10.1007/s10555-024-10220-8 · Cited by 17 · see citing works
Sammarco, A., Gomiero, C., Beffagna, G., Cavicchioli, L., Ferro, S., Michieletto, S., Orvieto, E., Patruno, M., & Zappulli, V. (2023) · Animals · doi:10.3390/ani13050878 · Cited by 16 · see citing works
Liu, X., & Wang, K. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1166668 · Cited by 15 · see citing works
Guan, J., Zhang, Z., Sun, J., Wang, X.-P., Zhou, Z., & Qin, L. (2023) · Clinical & Experimental Metastasis · doi:10.1007/s10585-023-10213-x · Cited by 14 · see citing works
Lack of basic rationale in epithelial-mesenchymal transition and its related concepts
Cao, Y. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01282-w · Cited by 14 · see citing works
BIRC5: A novel therapeutic target for lung cancer stem cells and glioma stem cells
Kahm, Y.-J., & Kim, R.-K. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.10.008 · Cited by 13 · see citing works
Song, B., Wei, F., Peng, J., Wei, X., Liu, M., Nie, Z., Ma, Y., & Peng, T. (2024) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b23-00668 · Cited by 13 · see citing works
Characteristics of Cancer Stem Cells and Their Potential Role in Endometrial Cancer
Frąszczak, K., & Barczyński, B. (2024) · Cancers · doi:10.3390/cancers16061083 · Cited by 13 · see citing works
Wang, K., Liu, S., Dou, Z., Zhang, S., & Yang, X. (2021) · Cancer Science · doi:10.1111/cas.15100 · Cited by 13 · see citing works
Takatani‐Nakase, T., Matsui, C., Hosotani, M., Omura, M., Takahashi, K., & Nakase, I. (2022) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.113006 · Cited by 13 · see citing works
The Role of Epithelial-to-Mesenchymal Transition in Cutaneous Squamous Cell Carcinoma
Fernández‐Figueras, M. T., & Puig, L. (2020) · Current Treatment Options in Oncology · doi:10.1007/s11864-020-00735-x · Cited by 13 · see citing works
Cancer stem cells in hepatocellular carcinoma: therapy resistance and emerging treatments
Yadav, D. K., Yadav, R. K., Singh, A., Huang, Y., Bao, D., Yang, Z., Huang, H., Jiang, Y., Wang, P., Lin, S., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1704868 · Cited by 12 · see citing works
Peyvandi, S., Bulliard, M., Yilmaz, A., Kauzlaric, A., Marcone, R., Haerri, L., Coquoz, O., Huang, Y.-T., Duffey, N., Gafner, L., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci166847 · Cited by 12 · see citing works
Impact of Epithelial–Mesenchymal Transition on the Immune Landscape in Breast Cancer
Khadri, F.-Z., Issac, M. S. M., & Gaboury, L. A. (2021) · Cancers · doi:10.3390/cancers13205099 · Cited by 12 · see citing works
Gulla, A., Andriusaityte, U., Zdanys, G., Babonaite, E., Strupas, K., & Kelly, H. M. (2022) · Medicina · doi:10.3390/medicina58040467 · Cited by 12 · see citing works
CSRP2 promotes cell stemness in head and neck squamous cell carcinoma
Zhang, M., Liu, J., Wan, S., Li, J., Wang, S., Fidèle, N. B., Huang, C., & Sun, Z. (2023) · Head & Neck · doi:10.1002/hed.27464 · Cited by 11 · see citing works
Chedere, A., Hari, K., Kumar, S., Rangarajan, A., & Jolly, M. K. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10030472 · Cited by 11 · see citing works
Self-citationModvig, S., Jeyakumar, J., Marquart, H. V., & Christensen, C. (2023) · Cancers · doi:10.3390/cancers15092504 · Cited by 12 · see citing works
Photodynamic therapy in cancer stem cells — state of the art
Ibarra, A. M. C., Aguiar, E. M. G., Ferreira, C. B. R., Siqueira, J. M., Côrrea, L., Nunes, F. D., Franco, A. L. D. S., Cecatto, R. B., Hamblin, M. R., & Rodrigues, M. F. S. D. (2023) · Lasers in Medical Science · doi:10.1007/s10103-023-03911-1 · Cited by 11 · see citing works
Bao, W., Qu, X., Wang, Y., Huang, D. Y., Zhang, H., Dong, M., Sun, H., Yang, Z., & Li, X. (2026) · MedComm · doi:10.1002/mco2.70599 · Cited by 11 · see citing works
Yao, L., & Zhang, X. (2022) · Journal of Cancer · doi:10.7150/jca.73143 · Cited by 10 · see citing works
Immune evasion by cancer stem cells ensures tumor initiation and failure of immunotherapy
Chakraborty, S., Mukherjee, S., Basak, U., Pati, S., Dutta, A., Dutta, S., Dhar, S., Sarkar, T., Guin, A., Sa, G., et al. (2023) · Exploration of Immunology · doi:10.37349/ei.2023.00108 · Cited by 11 · see citing works
ALDH1A1 as a marker for metastasis initiating cells: A mechanistic insight
Datta, N., Snijesh, V. P., Parvathy, K., Sneha, A., & Maliekal, T. T. (2024) · Experimental Cell Research · doi:10.1016/j.yexcr.2024.114213 · Cited by 10 · see citing works
Yao, Q., Lv, S., Xie, C., Du, S., & Yao, J. (2024) · Journal of Controlled Release · doi:10.1016/j.jconrel.2024.11.058 · Cited by 11 · see citing works
Bhoumik, S., & Lee, Y. (2025) · Cells · doi:10.3390/cells14070517 · Cited by 11 · see citing works
Plexin-B3 Regulates Cellular Motility, Invasiveness, and Metastasis in Pancreatic Cancer
Saxena, S., Prajapati, D. R., Goel, P., Tomar, B., Hayashi, Y., Atri, P., Rachagani, S., Grandgenett, P. M., Hollingsworth, M. A., Batra, S. K., et al. (2021) · Cancers · doi:10.3390/cancers13040818 · Cited by 10 · see citing works
Ma, K., Chen, H., Wang, K., Han, X., Zhang, Y., Wang, H., Hu, Z., & Wang, J. (2022) · Journal of Functional Foods · doi:10.1016/j.jff.2022.105219 · Cited by 10 · see citing works
Takao, T., Masuda, H., Kajitani, T., Miki, F., Miyazaki, K., Yoshimasa, Y., Katakura, S., Tomisato, S., Uchida, S., Uchida, H., et al. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02888-y · Cited by 10 · see citing works
Role of Epiregulin in Lung Tumorigenesis and Therapeutic Resistance
Sunaga, N., Miura, Y., Masuda, T., & Sakurai, R. (2024) · Cancers · doi:10.3390/cancers16040710 · Cited by 9 · see citing works
Cancer stem cells: Masters of all traits
Leck, L. Y. W., El-Aziz, Y. S. A., McKelvey, K. J., Park, K. C., Sahni, S., Lane, D. J. R., Skoda, J., & Jansson, P. J. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2024.167549 · Cited by 9 · see citing works
Lai, Y., Wang, B., & Zheng, X. (2022) · Methods in cell biology · doi:10.1016/bs.mcb.2022.04.010 · Cited by 9 · see citing works
Therapeutic Approaches of Dual-targeted Nanomedicines for Tumor Multidrug Resistance
Han, W., Shen, Z., Zou, J., Ye, Q., Cheng, G., Zhao, Y., Wang, T., & Chen, Y. (2023) · Current Drug Delivery · doi:10.2174/1567201820666230504145614 · Cited by 9 · see citing works
Peng, Z., Wang, S., Wen, D., Mei, Z., Zhang, H., Liao, S., Lv, L., & Li, C. (2024) · Translational Oncology · doi:10.1016/j.tranon.2024.101916 · Cited by 9 · see citing works
Hu, M., Dai, C., Sun, X., Chen, Y., Xu, N., Lin, Z., Xu, S., Cheng, C., Tan, Z., Bian, S., et al. (2024) · Functional & Integrative Genomics · doi:10.1007/s10142-024-01310-5 · Cited by 8 · see citing works
Neves, S. P., Bomfim, L. M., Kataura, T., Carvalho, S. G., Nogueira, M. L., Dias, R. B., Valverde, L. D. F., Rocha, C. A. G., Soares, M. B. P., da Silva, M. M., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117059 · Cited by 8 · see citing works
GATAD2B O-GlcNAcylation Regulates Breast Cancer Stem-like Potential and Drug Resistance
Minh, G. L., Merzy, J., Esquea, E. M., Ahmed, N. N., Young, R. G., Sharp, R. J., Dhameliya, T. T., Agana, B. A., Lee, M., Bethard, J. R., et al. (2025) · Cells · doi:10.3390/cells14060398 · Cited by 8 · see citing works
Krishnan, R. P., Pandiar, D., Ramani, P., Ramalingam, K., & Jayaraman, S. (2023) · Cureus · doi:10.7759/cureus.42899 · Cited by 8 · see citing works
Алексеенко, И. В., Kondratyeva, L. G., Чернов, И. П., & Sverdlov, E. D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032796 · Cited by 8 · see citing works
Mannion, A. J., Odell, A. F., Baker, S. M., Matthews, L. C., Jones, P. F., & Cook, G. P. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1129015 · Cited by 7 · see citing works
Beyond boundaries: unraveling innovative approaches to combat bone-metastatic cancers
Lan, H., Wu, B., Jin, K., & Chen, Y. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1260491 · Cited by 6 · see citing works
Tn antigen promotes breast cancer metastasis via impairment of CASC4
Li, R., Dong, X., Chen, S., Tan, J.-Y. B., Chen, X., Liu, J., Wen, T., & Ru, X. (2023) · Cell Biology International · doi:10.1002/cbin.12077 · Cited by 7 · see citing works
Chaudhary, P., Yadav, K., Lee, H. J., Kang, K. W., Mo, J., & Kim, J. (2024) · Breast Cancer Research · doi:10.1186/s13058-024-01827-4 · Cited by 7 · see citing works
- Authors
- Celià-Terrassa, T., & Jolly, M. K.
- Affiliations
- Municipal Institute for Medical Research (ES)
- Indian Institute of Science Bangalore (IN)
- Venue
- Cold Spring Harbor Perspectives in Medicine
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2019-09-30
- Volume
- 10
- Issue
- 7
- Pages
- a036905
- ISSN
- 2157-1422 (ISSN-L)
- PMC
- PMC7328448
- OpenAlex
- W2978226446
- Cited by
- 163
- References
- 160
- Citations by year
- 2026: 14 · 2025: 23 · 2024: 32 · 2023: 25 · 2022: 31 · 2021: 26 · 2020: 10 · 2019: 2
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cold Spring Harbor Perspectives in Medicine (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Repositori digital de la UPF (Universitat Pompeu Fabra) (publishedVersion, cc-by-nc)
- Funders
- Cancer Research Institute
- Science and Engineering Research Board (SB/S2/RJN 049/2018)
- Instituto de Salud Carlos III (PI18/00014)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- cancer stem cells, epithelial-mesenchymal transition, mesenchymal-epithelial transition, metastasis, cellular plasticity, tumor heterogeneity, metastatic colonization
- MeSH terms
- Humans, Neoplasm Metastasis, Neoplasms, Neoplastic Stem Cells, Epithelial-Mesenchymal Transition
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