TGFβ signaling directs serrated adenomas to the mesenchymal colorectal cancer subtype
Open accessAbstract
The heterogeneous nature of colorectal cancer (CRC) complicates prognosis and is suggested to be a determining factor in the efficacy of adjuvant therapy for individual patients. Based on gene expression profiling, CRC is currently classified into four consensus molecular subtypes (CMSs), characterized by specific biological programs, thus suggesting the existence of unifying developmental drivers for each CMS. Using human organoid cultures, we investigated the role of such developmental drivers at the premalignant stage of distinct CRC subtypes and found that TGFβ plays an important role in the development of the mesenchymal CMS4, which is of special interest due to its association with dismal prognosis. We show that in tubular adenomas (TAs), which progress to classical CRCs, the dominating response to TGFβ is death by apoptosis. By contrast, induction of a mesenchymal phenotype upon TGFβ treatment prevails in a genetically engineered organoid culture carrying a BRAFV600E mutation, constituting a model system for sessile serrated adenomas (SSAs). Our data indicate that TGFβ signaling is already active in SSA precursor lesions and that TGFβ is a critical cue for directing SSAs to the mesenchymal, poor‐prognosis CMS4 of CRC. Sessile serrated adenomas (SSAs)—precursor lesions of the serrated neoplasia pathway to colorectal cancer (CRC)—are predicted to give rise to either the good‐ or the poor‐prognosis CRC consensus molecular subtype (CMS1 and CMS4, respectively). Sessile serrated adenomas (SSAs)—precursor lesions of the serrated neoplasia pathway to colorectal cancer (CRC)—are predicted to give rise to either the good‐ or the poor‐prognosis CRC consensus molecular subtype (CMS1 and CMS4, respectively).
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?
TGFβ can direct human organoid cultures to a CMS4 profile.
“Follow-up studies have documented that TGFβ can direct human organoid cultures to a CMS4 profile (20)”
From Clinical Challenges of Consensus Molecular Subtype CMS4 Colon Cancer in the Era of Precision Medicine (2024) · cites this paper as [20]
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
Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506580102 · Cited by 53,625 · see citing works
limma powers differential expression analyses for RNA-sequencing and microarray studies
Ritchie, M. E., Phipson, B., Wu, D., Hu, Y., Law, C. W., Shi, W., & Smyth, G. K. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv007 · Cited by 40,458 · see citing works
Multiplex Genome Engineering Using CRISPR/Cas Systems
Cong, L., Ran, F. A., Cox, D., Lin, S., Barretto, R., Habib, N., Hsu, P. D., Wu, X., Jiang, W., Marraffini, L. A., et al. (2013) · Science · doi:10.1126/science.1231143 · Cited by 15,339 · see citing works
A genetic model for colorectal tumorigenesis
Fearon, E. R., & Vogelstein, B. (1990) · Cell · doi:10.1016/0092-8674(90)90186-i · Cited by 12,132 · see citing works
Mootha, V. K., Lindgren, C. M., Eriksson, K.-F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstråle, M., Laurila, E., et al. (2003) · Nature Genetics · doi:10.1038/ng1180 · Cited by 10,197 · see citing works
RNA-Guided Human Genome Engineering via Cas9
Mali, P., Yang, L., Esvelt, K. M., Aach, J., Guell, M., DiCarlo, J. E., Norville, J. E., & Church, G. M. (2013) · Science · doi:10.1126/science.1232033 · Cited by 9,210 · 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
Adjusting batch effects in microarray expression data using empirical Bayes methods
Johnson, W. E., Li, C., & Rabinovic, A. (2007) · Biostatistics · doi:10.1093/biostatistics/kxj037 · Cited by 8,658 · see citing works
Comprehensive molecular characterization of human colon and rectal cancer
The Cancer Genome Atlas Network (2012) · Nature · doi:10.1038/nature11252 · Cited by 8,499 · 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
The consensus molecular subtypes of colorectal cancer
Guinney, J., Dienstmann, R., Wang, X., de Reyniès, A., Schlicker, A., Soneson, C., Marisa, L., Roepman, P., Nyamundanda, G., Angelino, P., et al. (2015) · Nature Medicine · doi:10.1038/nm.3967 · Cited by 5,170 · see citing works
Self-citationSummaries of Affymetrix GeneChip probe level data
Irizarry, R. A. (2003) · Nucleic Acids Research · doi:10.1093/nar/gng015 · Cited by 4,906 · see citing works
Nicoletti, I., Migliorati, G., Pagliacci, M. C., Grignani, F., & Riccardi, C. (1991) · Journal of Immunological Methods · doi:10.1016/0022-1759(91)90198-o · Cited by 4,580 · see citing works
Massagué, J. (2008) · Cell · doi:10.1016/j.cell.2008.07.001 · Cited by 3,907 · see citing works
Sato, T., Stange, D. E., Ferrante, M., Vries, R. G. J., van Es, J. H., van den Brink, S., van Houdt, W. J., Pronk, A., van Gorp, J., Siersema, P. D., et al. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.07.050 · Cited by 3,753 · see citing works
Self-citationMassagué, J. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3434 · Cited by 3,130 · see citing works
Prospective Derivation of a Living Organoid Biobank of Colorectal Cancer Patients
van de Wetering, M., Francies, H. E., Francis, J. M., Bounova, G., Iorio, F., Pronk, A., van Houdt, W., van Gorp, J., Taylor-Weiner, A., Kester, L., et al. (2015) · Cell · doi:10.1016/j.cell.2015.03.053 · Cited by 2,408 · see citing works
Self-citationInactivation of the Type II TGF-β Receptor in Colon Cancer Cells with Microsatellite Instability
Markowitz, S. D., Wang, J., Myeroff, L. L., Parsons, R. E., Sun, L., Lutterbaugh, J., Fan, R. S., Zborowska, E., Kinzler, K. W., Vogelstein, B., et al. (1995) · Science · doi:10.1126/science.7761852 · Cited by 2,267 · see citing works
The evolution of cancer of the colon and rectum
Muto, T., Bussey, H. J. R., & Morson, B. C. (1975) · Cancer · doi:10.1002/cncr.2820360944 · Cited by 2,124 · 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
pl5INK4B is a potentia| effector of TGF-β-induced cell cycle arrest
Hannon, G. J., & Beach, D. (1994) · Nature · doi:10.1038/371257a0 · Cited by 1,950 · see citing works
Targeted genome engineering in human cells with the Cas9 RNA-guided endonuclease
Cho, S. W., Kim, S., Kim, J. M., & Kim, J.-S. (2013) · Nature Biotechnology · doi:10.1038/nbt.2507 · Cited by 1,863 · 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
Marisa, L., de Reyniès, A., Duval, A., Selves, J., Gaub, M. P., Vescovo, L., Etienne-Grimaldi, M.-C., Schiappa, R., Guenot, D., Ayadi, M., et al. (2013) · PLoS Medicine · doi:10.1371/journal.pmed.1001453 · Cited by 1,507 · see citing works
Jass, J. R. (2006) · Histopathology · doi:10.1111/j.1365-2559.2006.02549.x · Cited by 1,381 · see citing works
Stromal gene expression defines poor-prognosis subtypes in colorectal cancer
Calon, A., Lonardo, E., Berenguer-Llergo, A., Espinet, E., Hernando-Momblona, X., Iglesias, M., Sevillano, M., Palomo-Ponce, S., Tauriello, D. V. F., Byrom, D., et al. (2015) · Nature Genetics · doi:10.1038/ng.3225 · Cited by 1,070 · see citing works
Sequential cancer mutations in cultured human intestinal stem cells
Drost, J., van Jaarsveld, R. H., Ponsioen, B., Zimberlin, C., van Boxtel, R., Buijs, A., Sachs, N., Overmeer, R. M., Offerhaus, G. J., Begthel, H., et al. (2015) · Nature · doi:10.1038/nature14415 · Cited by 1,067 · see citing works
Self-citationDependency of Colorectal Cancer on a TGF-β-Driven Program in Stromal Cells for Metastasis Initiation
Calon, A., Espinet, E., Palomo-Ponce, S., Tauriello, D. V. F., Iglesias, M., Céspedes, M. V., Sevillano, M., Nadal, C., Jung, P., Zhang, X. H.-F., et al. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.08.013 · Cited by 1,060 · see citing works
Taube, J. H., Herschkowitz, J. I., Komurov, K., Zhou, A. Y., Gupta, S. K., Yang, J., Hartwell, K. A., Önder, T. T., Gupta, P. B., Evans, K. W., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004900107 · Cited by 1,041 · see citing works
Role of the Serrated Pathway in Colorectal Cancer Pathogenesis
Leggett, B., & Whitehall, V. (2010) · Gastroenterology · doi:10.1053/j.gastro.2009.12.066 · Cited by 979 · see citing works
Sadanandam, A., Lyssiotis, C. A., Homicsko, K., Collisson, E. A., Gibb, W. J., Wullschleger, S., Ostos, L. C. G., Lannon, W. A., Grotzinger, C., Del Rio, M., et al. (2013) · Nature Medicine · doi:10.1038/nm.3175 · Cited by 960 · see citing works
Datto, M., Li, Y., Panus, J. F., Howe, D. J., Xiong, Y., & Wang, X. F. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.12.5545 · Cited by 945 · see citing works
Self-citationMoustakas, A., & Heldin, C. (2007) · Cancer Science · doi:10.1111/j.1349-7006.2007.00550.x · Cited by 798 · see citing works
De Sousa E Melo, F., Wang, X., Jansen, M., Fessler, E., Trinh, A., de Rooij, L. P. M. H., de Jong, J. H., de Boer, O. J., van Leersum, R., Bijlsma, M. F., et al. (2013) · Nature Medicine · doi:10.1038/nm.3174 · Cited by 771 · see citing works
Self-citationBRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum
Kambara, T., Simms, L. A., Whitehall, V., Spring, K. J., Wynter, C. V. A., Walsh, M. D., Barker, M., Arnold, S., McGivern, A., Matsubara, N., et al. (2004) · Gut · doi:10.1136/gut.2003.037671 · Cited by 721 · see citing works
Update on the serrated pathway to colorectal carcinoma
Snover, D. C. (2010) · Human Pathology · doi:10.1016/j.humpath.2010.06.002 · Cited by 642 · see citing works
Stromal contribution to the colorectal cancer transcriptome
Isella, C., Terrasi, A., Bellomo, S. E., Petti, C., Galatola, G., Muratore, A., Mellano, A., Senetta, R., Cassenti, A., Sonetto, C., et al. (2015) · Nature Genetics · doi:10.1038/ng.3224 · Cited by 640 · see citing works
Mechanism of TGF-β signaling to growth arrest, apoptosis, and epithelial–mesenchymal transition
Heldin, C., Landström, M., & Moustakas, A. (2009) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2009.01.021 · Cited by 633 · see citing works
TGF-β Tumor Suppression through a Lethal EMT
David, C. J., Huang, Y.-H., Chen, M., Su, J., Zou, Y., Bardeesy, N. M., Iacobuzio–Donahue, C. A., & Massagué, J. (2016) · Cell · doi:10.1016/j.cell.2016.01.009 · Cited by 597 · see citing works
Spaderna, S., Schmalhofer, O., Hlubek, F., Berx, G., Eger, A., Merkel, S., Jung, A., Kirchner, T., & Brabletz, T. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.06.016 · Cited by 477 · see citing works
CDX2 as a Prognostic Biomarker in Stage II and Stage III Colon Cancer
Dalerba, P. D., Sahoo, D., Paik, S., Guo, X., Yothers, G., Song, N., Wilcox-Fogel, N., Forgó, E., Rajendran, P. S., Miranda, S. P., et al. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1506597 · Cited by 470 · see citing works
MED12 Controls the Response to Multiple Cancer Drugs through Regulation of TGF-β Receptor Signaling
Huang, S., Hölzel, M., Knijnenburg, T., Schlicker, A., Roepman, P., McDermott, U., Garnett, M., Grernrum, W., Sun, C., Prahallad, A., et al. (2012) · Cell · doi:10.1016/j.cell.2012.10.035 · Cited by 430 · see citing works
Gene expression patterns unveil a new level of molecular heterogeneity in colorectal cancer
Budínská, E., Popovici, V. C., Tejpar, S., D’Ario, G., Lapique, N., Sikora, K. O., Narzo, A. F. D., Yan, P., Hodgson, J., Weinrich, S. L., et al. (2013) · The Journal of Pathology · doi:10.1002/path.4212 · Cited by 409 · see citing works
Association Between Molecular Subtypes of Colorectal Cancer and Patient Survival
Phipps, A. I., Limburg, P. J., Baron, J. A., Burnett‐Hartman, A. N., Weisenberger, D. J., Laird, P. W., Sinicrope, F. A., Rosty, C., Buchanan, D. D., Potter, J. D., et al. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.09.038 · Cited by 403 · see citing works
TGF-β induces apoptosis through Smad-mediated expression of DAP-kinase
Jang, C., Chen, C.-H., Chen, C., Chen, J., Su, Y., & Chen, R. (2001) · Nature Cell Biology · doi:10.1038/ncb731 · Cited by 387 · 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
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
Roepman, P., Schlicker, A., Tabernero, J. M., Majewski, I. J., Tian, S., Moreno, V. R., Snel, M. H. J., Chresta, C. M., Rosenberg, R., Nitsche, U., et al. (2013) · International Journal of Cancer · doi:10.1002/ijc.28387 · Cited by 341 · see citing works
Melo, F. D. S. E., Çolak, S., Buikhuisen, J. Y., Köster, J., Cameron, K., de Jong, J. H., Tuynman, J. B., Prasetyanti, P. R., Fessler, E., van den Bergh, S., et al. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.10.008 · Cited by 333 · see citing works
Self-citationSessile serrated adenomas: prevalence of dysplasia and carcinoma in 2139 patients
Lash, R. H., Genta, R. M., & Schuler, C. M. (2010) · Journal of Clinical Pathology · doi:10.1136/jcp.2010.075507 · Cited by 333 · see citing works
SMAD2 , SMAD3 and SMAD4 Mutations in Colorectal Cancer
Fleming, N. I., Jorissen, R. N., Mouradov, D., Christie, M., Sakthianandeswaren, A., Palmieri, M., Day, F. L., Li, S., Tsui, C., Lipton, L. R., et al. (2012) · Cancer Research · doi:10.1158/0008-5472.can-12-2706 · Cited by 327 · see citing works
Shioiri, M., Shida, T., Koda, K., Oda, K., Seike, K., Nishimura, M., Takano, S., & Miyazaki, M. (2006) · British Journal of Cancer · doi:10.1038/sj.bjc.6603193 · Cited by 287 · see citing works
Schlicker, A., Beran, G. J., Chresta, C. M., McWalter, G., Pritchard, A., Weston, S. L., Runswick, S. K., Davenport, S., Heathcote, K., Alférez, D., et al. (2012) · BMC Medical Genomics · doi:10.1186/1755-8794-5-66 · Cited by 253 · see citing works
Frequent CpG Island Methylation in Serrated Adenomas of the Colorectum
Park, S. J., Rashid, A., Lee, J.-H., Kim, S. G., Hamilton, S. R., & Wu, T. (2003) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63878-3 · Cited by 239 · see citing works
The evolution of cancer of the colon and rectum
Muto, T., Bussey, H. J. R., & Morson, B. C. (1975) · Cancer · doi:10.1002/cncr.2820360644 · Cited by 237 · see citing works
Serrated neoplasia—role in colorectal carcinogenesis and clinical implications
IJspeert, J. E. G., Vermeulen, L., Meijer, G. A., & Dekker, E. (2015) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2015.73 · Cited by 191 · see citing works
Self-citationGröger, C., Grubinger, M., Waldhoer, T., Vierlinger, K., & Mikulits, W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051136 · Cited by 184 · see citing works
Friedman, E. D., Gold, L. I., Klimstra, D., Zeng, Z., Winawer, S. J., & Cohen, A. M. (1995) · PubMed · Cited by 182 · see citing works
Smad Signaling Is Required to Maintain Epigenetic Silencing during Breast Cancer Progression
Papageorgis, P., Lambert, A. W., Ozturk, S., Gao, F., Pan, H., Manne, U., Alekseyev, Y. O., Thiagalingam, A., Abdolmaleky, H. M., Lenburg, M. E., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-1872 · Cited by 177 · see citing works
Tsushima, H., Ito, N., Tamura, S., Matsuda, Y., Inada, M., Yabuuchi, I., Imai, Y., Nagashima, R., Misawa, H., Takeda, H., et al. (2001) · PubMed · Cited by 149 · see citing works
Carragher, L. A. S., Snell, K. R., Giblett, S. M., Aldridge, V. S. S., Patel, B., Cook, S. J., Winton, D. J., Marais, R., & Pritchard, C. A. (2010) · EMBO Molecular Medicine · doi:10.1002/emmm.201000099 · Cited by 144 · see citing works
Pérez‐Villamil, B., Romera-López, A., Prieto, S. H., López–Campos, G., Calles, A., Asenjo, J. A. L., Sanz‐Ortega, J., Fernández, C., Sastre, J., Alfonso, R., et al. (2012) · BMC Cancer · doi:10.1186/1471-2407-12-260 · Cited by 126 · see citing works
Progression of a Sessile Serrated Adenoma to an Early Invasive Cancer Within 8 Months
Oono, Y., Fu, K., Nakamura, H., Iriguchi, Y., Yamamura, A., Tomino, Y., Oda, J., Mizutani, M., Takayanagi, S., Kishi, D., et al. (2008) · Digestive Diseases and Sciences · doi:10.1007/s10620-008-0407-7 · Cited by 125 · see citing works
TGF-β: An emerging player in drug resistance
Brunen, D., Willems, S., Kellner, U., Midgley, R., Simon, I., & Bernards, R. (2013) · Cell Cycle · doi:10.4161/cc.26034 · Cited by 124 · see citing works
Robson, H., Anderson, E., James, R., & Schofield, P. F. (1996) · British Journal of Cancer · doi:10.1038/bjc.1996.432 · Cited by 103 · see citing works
Lurkin, I., Stoehr, R., Hurst, C. D., van Tilborg, A. A. G., Knowles, M. A., Hartmann, A., & Zwarthoff, E. C. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008802 · Cited by 95 · see citing works
Ramesh, S., Qi, X., Wildey, G. M., Robinson, J., Molkentin, J. D., Letterio, J. J., & Howe, P. H. (2008) · EMBO Reports · doi:10.1038/embor.2008.158 · Cited by 87 · see citing works
Prasetyanti, P. R., Zimberlin, C. D., Bots, M. L., Vermeulen, L., Melo, F. D. S. E., & Medema, J. P. (2013) · Molecular Cancer · doi:10.1186/1476-4598-12-126 · Cited by 62 · see citing works
Self-citationOncogenic mutations in intestinal adenomas regulate Bim-mediated apoptosis induced by TGF-β
Wiener, Z., Band, A. M., Kallio, P., Hogstrom, J. M., Hyvönen, V., Kaijalainen, S., Ritvos, O., Haglund, C. H., Kruuna, O., Robine, S., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1406444111 · Cited by 58 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Drost, J., & Clevers, H. (2018) · Nature Reviews Cancer · doi:10.1038/s41568-018-0007-6 · Cited by 1,790 · see citing works
Self-citationConsensus molecular subtypes and the evolution of precision medicine in colorectal cancer
Dienstmann, R., Vermeulen, L., Guinney, J., Kopetz, S., Tejpar, S., & Tabernero, J. M. (2017) · Nature reviews. Cancer · doi:10.1038/nrc.2016.126 · Cited by 1,038 · see citing works
Self-citationTargeting TGF-β Signaling in Cancer
Colak, S., & ten Dijke, P. (2017) · Trends in cancer · doi:10.1016/j.trecan.2016.11.008 · Cited by 1,003 · see citing works
Lineage-dependent gene expression programs influence the immune landscape of colorectal cancer
Lee, H., Hong, Y., Etlioglu, H. E., Cho, Y. B., Pomella, V., den Bosch, B. V., Vanhecke, J., Verbandt, S., Hong, H.-K., Min, J.-W., et al. (2020) · Nature Genetics · doi:10.1038/s41588-020-0636-z · Cited by 916 · see citing works
Epigenetics of colorectal cancer: biomarker and therapeutic potential
Jung, G., Hernández-Illán, E., Moreira, L., Balaguer, F., & Goel, A. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0230-y · Cited by 813 · see citing works
Fiori, M. E., Franco, S. D., Villanova, L., Bianca, P., Stassi, G., & Maria, R. D. (2019) · Molecular Cancer · doi:10.1186/s12943-019-0994-2 · Cited by 648 · see citing works
Pathways of Colorectal Carcinogenesis
Nguyen, L. H., Goel, A., & Chung, D. C. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.08.059 · Cited by 606 · see citing works
Clinical management of metastatic colorectal cancer in the era of precision medicine
Ciardiello, F., Ciardiello, D., Martini, G., Napolitano, S., Tabernero, J. M., & Cervantes, A. M. R. (2022) · CA A Cancer Journal for Clinicians · doi:10.3322/caac.21728 · Cited by 537 · see citing works
Jackstadt, R., van Hooff, S. R., Leach, J. D. G., Cortés-Lavaud, X., Lohuis, J. O., Ridgway, R. A., Wouters, V. M., Roper, J., Kendall, T. J., Roxburgh, C. S. D., et al. (2019) · Cancer Cell · doi:10.1016/j.ccell.2019.08.003 · Cited by 427 · see citing works
Self-citationTargeting TGFβ signal transduction for cancer therapy
Liu, S., Ren, J., & ten Dijke, P. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-00436-9 · Cited by 413 · see citing works
“For example, by performing intermittent dosing strategies bypassing cardiovascular toxicity,(321,322) by specifically inhibiting only the TGFβ1 isoform that has the strongest link with cancer progression,(282) or by selecting cancer patients for treatment with a mesenchymal phenotype and high TGFβ activity that are li…”
BackgroundTesta, U., Pelosi, E., & Castelli, G. (2018) · Medical Sciences · doi:10.3390/medsci6020031 · Cited by 380 · see citing works
Organoid technology and applications in cancer research
Xu, H., Lyu, X., Yi, M., Zhao, W., Song, Y., & Wu, K. (2018) · Journal of Hematology & Oncology · doi:10.1186/s13045-018-0662-9 · Cited by 350 · see citing works
Cancer‐associated fibroblasts in breast cancer: Challenges and opportunities
Hu, D., Li, Z., Zheng, B., Lin, X., Pan, Y., Gong, P., Zhuo, W., Hu, Y., Chen, C., Chen, L., et al. (2022) · 癌症:英文版 · doi:10.1002/cac2.12291 · Cited by 293 · see citing works
Transforming Growth Factor-β Signaling Pathway in Colorectal Cancer and Its Tumor Microenvironment
Itatani, Y., Kawada, K., & Sakai, Y. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20235822 · Cited by 243 · see citing works
Transforming Growth Factor β Superfamily Signaling in Development of Colorectal Cancer
Jung, B. H., Staudacher, J. J., & Beauchamp, D. R. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.10.015 · Cited by 242 · see citing works
Genetic and epigenetic characteristics of inflammatory bowel disease-associated colorectal cancer
Rajamäki, K., Taira, A., Katainen, R., Välimäki, N., Kuosmanen, A., Plaketti, R.-M., Seppälä, T. T., Ahtiainen, M., Wirta, E.-V., Vartiainen, E., et al. (2021) · Gastroenterology · doi:10.1053/j.gastro.2021.04.042 · Cited by 230 · see citing works
Distinct gut microbiome patterns associate with consensus molecular subtypes of colorectal cancer
Purcell, R. V., Visnovska, M., Biggs, P. J., Schmeier, S., & Frizelle, F. A. (2017) · Scientific Reports · doi:10.1038/s41598-017-11237-6 · Cited by 227 · see citing works
Apc-mutant cells act as supercompetitors in intestinal tumour initiation
van Neerven, S. M., de Groot, N. E., Nijman, L. E., Scicluna, B. P., van Driel, M. S., Lecca, M. C., Warmerdam, D. O., Kakkar, V., Moreno, L. F., Vieira Braga, F. A., et al. (2021) · Nature · doi:10.1038/s41586-021-03558-4 · Cited by 211 · see citing works
Self-citationTGF-β Signaling in Liver, Pancreas, and Gastrointestinal Diseases and Cancer
Gough, N. R., Xiang, X., & Mishra, L. (2021) · Gastroenterology · doi:10.1053/j.gastro.2021.04.064 · Cited by 204 · see citing works
Genome-Scale CRISPR Screening in Human Intestinal Organoids Identifies Drivers of TGF-β Resistance
Ringel, T., Frey, N., Ringnalda, F., Janjuha, S., Cherkaoui, S., Butz, S., Srivatsa, S., Pirkl, M., Russo, G., Villiger, L., et al. (2020) · Cell Stem Cell · doi:10.1016/j.stem.2020.02.007 · Cited by 202 · see citing works
Self-citationOrganoid models of gastrointestinal cancers in basic and translational research
Lau, H. C.-H., Kranenburg, O., Xiao, H., & Yu, J. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0255-2 · Cited by 195 · see citing works
CRISPR-Cas Tools and Their Application in Genetic Engineering of Human Stem Cells and Organoids
Hendriks, D. F. G., Clevers, H. C., & Artegiani, B. (2020) · Cell stem cell · doi:10.1016/j.stem.2020.10.014 · Cited by 196 · see citing works
Self-citationMolecular subtyping of colorectal cancer: Recent progress, new challenges and emerging opportunities
Wang, W., Kandimalla, R., Huang, H., Zhu, L., Li, Y., Gao, F., Goel, A., & Wang, X. (2018) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2018.05.002 · Cited by 189 · see citing works
Self-citationApplications of organoids for cancer biology and precision medicine
Lo, Y.-H., Karlsson, K., & Kuo, C. J. (2020) · Nature Cancer · doi:10.1038/s43018-020-0102-y · Cited by 182 · see citing works
Consensus molecular subtypes of colorectal cancer are recapitulated in in vitro and in vivo models
Linnekamp, J. F., van Hooff, S. R., Prasetyanti, P. R., Kandimalla, R., Buikhuisen, J. Y., Fessler, E., Ramesh, P., Lee, K. A. S. T., Bochove, G. G. W., de Jong, J. H., et al. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-017-0011-5 · Cited by 177 · see citing works
Self-citationSomatic cell-derived organoids as prototypes of human epithelial tissues and diseases
Fujii, M., & Sato, T. (2020) · Nature Materials · doi:10.1038/s41563-020-0754-0 · Cited by 165 · see citing works
Organoid cultures for cancer modeling
Yan, H. H. N., Chan, A., Lai, F. P.-L., & Leung, S. Y. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.05.012 · Cited by 163 · see citing works
The tumour–stroma ratio in colon cancer: the biological role and its prognostic impact
van Pelt, G. W., Sandberg, T. P., Morreau, H., Gelderblom, H., van Krieken, J. H. J. M., Tollenaar, R. A. E. M., & Mesker, W. E. (2018) · Histopathology · doi:10.1111/his.13489 · Cited by 155 · see citing works
Genetic wiring maps of single-cell protein states reveal an off-switch for GPCR signalling
Brockmann, M., Blomen, V. A., Nieuwenhuis, J., Stickel, E., Raaben, M., Bleijerveld, O. B., Altelaar, A. F. M., Jae, L. T., & Brummelkamp, T. R. (2017) · Nature · doi:10.1038/nature22376 · Cited by 140 · see citing works
CRISPR/Cas 9 genome editing and its applications in organoids
Driehuis, E., & Clevers, H. C. (2017) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00410.2016 · Cited by 154 · see citing works
Self-citationModeling Human Digestive Diseases With CRISPR-Cas9–Modified Organoids
Fujii, M., Clevers, H. C., & Sato, T. (2018) · Gastroenterology · doi:10.1053/j.gastro.2018.11.048 · Cited by 140 · see citing works
Self-citationOrganoid based personalized medicine: from bench to bedside
Li, Y., Tang, P., Cai, S., Peng, J., & Hua, G. (2020) · Cell Regeneration · doi:10.1186/s13619-020-00059-z · Cited by 138 · see citing works
Consensus Molecular Subtypes of Colorectal Cancer and their Clinical Implications.
Thanki, K. K., Nicholls, M. E., Gajjar, A. H., Senagore, A. J., Qiu, S., Szabó, C., Hellmich, M. R., & Chao, C. (2017) · PubMed · Cited by 136 · see citing works
Molecular subtypes in cancers of the gastrointestinal tract
Bijlsma, M. F., Sadanandam, A., Tan, P. B. O., & Vermeulen, L. (2017) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2017.33 · Cited by 130 · see citing works
Self-citationLannagan, T. R. M., Lee, Y. K., Wang, T., Roper, J., Bettington, M. L., Fennell, L., Vrbanac, L., Jonavicius, L., Somashekar, R., Gieniec, K. A., et al. (2018) · Gut · doi:10.1136/gutjnl-2017-315920 · Cited by 130 · see citing works
Cancer research using organoid technology
Kretzschmar, K. (2021) · Journal of Molecular Medicine · doi:10.1007/s00109-020-01990-z · Cited by 120 · see citing works
CRISPR/Cas9 Genome-Editing System in Human Stem Cells: Current Status and Future Prospects
Zhang, Z., Zhang, Y., Gao, F., Han, S., Cheah, K. S. E., Tse, H., & Lian, Q. (2017) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2017.09.009 · Cited by 116 · see citing works
Targeting the Microenvironment in Advanced Colorectal Cancer
Tauriello, D. V. F., & Batlle, E. (2016) · Trends in cancer · doi:10.1016/j.trecan.2016.08.001 · Cited by 104 · see citing works
The Use of Stem Cell-Derived Organoids in Disease Modeling: An Update
Azar, J. H., Bahmad, H. F., Daher, D., Moubarak, M. M., Hadadeh, O., Monzer, A., Bitar, S. A., Jamal, M., Al‐Sayegh, M., & Abou-Kheir, W. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147667 · Cited by 100 · see citing works
Exploring and modelling colon cancer inter-tumour heterogeneity: opportunities and challenges
Buikhuisen, J. Y., Torang, A., & Medema, J. P. (2020) · Oncogenesis · doi:10.1038/s41389-020-00250-6 · Cited by 92 · see citing works
Self-citationConsensus molecular subtype classification of colorectal adenomas
Komor, M. A., Bosch, L. J., Bounova, G., Bolijn, A. S., Delis‐van Diemen, P. M., Rausch, C., Hoogstrate, Y., Stubbs, A. P., de Jong, M., Jenster, G., et al. (2018) · The Journal of Pathology · doi:10.1002/path.5129 · Cited by 86 · see citing works
Back to the Colorectal Cancer Consensus Molecular Subtype Future
Menter, D. G., Davis, J. S., Broom, B. M., Overman, M. J., Morris, J. S., & Kopetz, S. (2019) · Current Gastroenterology Reports · doi:10.1007/s11894-019-0674-9 · Cited by 81 · see citing works
Martens, S., Lefesvre, P., Nicolle, R., Biankin, A. V., Puleo, F., Laethem, J. V., & Rooman, I. (2019) · Annals of Oncology · doi:10.1093/annonc/mdz181 · Cited by 78 · see citing works
Smit, W. L., Spaan, C. N., de Boer, R. J., Ramesh, P., Garcia, T. M., Meijer, B. J., Vermeulen, J. L. M., Lezzerini, M., MacInnes, A. W., Köster, J., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1912772117 · Cited by 77 · see citing works
Self-citationColorectal Cancer Subtypes: Developmental Origin and Microenvironmental Regulation
Fessler, E., & Medema, J. P. (2016) · Trends in cancer · doi:10.1016/j.trecan.2016.07.008 · Cited by 74 · see citing works
Self-citationGenetic engineering in organoids
Teriyapirom, I., Batista-Rocha, A. S., & Koo, B.-K. (2021) · Journal of Molecular Medicine · doi:10.1007/s00109-020-02029-z · Cited by 68 · see citing works
Investigation of colorectal cancer in accordance with consensus molecular subtype classification
Sawayama, H., Miyamoto, Y., Ogawa, K., Yoshida, N., & Baba, H. (2020) · Annals of Gastroenterological Surgery · doi:10.1002/ags3.12362 · Cited by 60 · see citing works
Organoids and Colorectal Cancer
Barbáchano, A., Fernández‐Barral, A., Bustamante‐Madrid, P., Prieto, I., Rodrı́guez-Salas, N., Larriba, M. J., & Múñoz, A. (2021) · Cancers · doi:10.3390/cancers13112657 · Cited by 68 · see citing works
Overexpression of POSTN in Tumor Stroma Is a Poor Prognostic Indicator of Colorectal Cancer
Oh, H. J., Bae, J. M., Wen, X.-Y., Cho, N., Kim, J. H., & Kang, G. H. (2017) · Journal of Pathology and Translational Medicine · doi:10.4132/jptm.2017.01.19 · Cited by 65 · see citing works
Elastin is a key factor of tumor development in colorectal cancer
Li, J., Xu, X., Jiang, Y., Hansbro, N. G., Hansbro, P. M., Xu, J., & Liu, G. (2020) · BMC Cancer · doi:10.1186/s12885-020-6686-x · Cited by 64 · see citing works
Middleton, G., Yang, Y., Campbell, C. D., André, T., Atreya, C. E., Schellens, J. H. M., Yoshino, T., Bendell, J. C., Hollebecque, A., McRee, A. J., et al. (2020) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-19-3579 · Cited by 63 · see citing works
CDX2 prognostic value in stage II/III resected colon cancer is related to CMS classification
Pilati, C., Taı̈eb, J., Balogoun, R., Marisa, L., de Reyniès, A., & Laurent‐Puig, P. (2017) · Annals of Oncology · doi:10.1093/annonc/mdx066 · Cited by 59 · see citing works
Bond, C., Liu, C., Kawamata, F., McKeone, D., Fernando, W., Jamieson, S., Pearson, S., Kane, A. M., Woods, S. L., Lannagan, T. R. M., et al. (2018) · Epigenetics · doi:10.1080/15592294.2017.1411446 · Cited by 59 · see citing works
Colorectal premalignancy is associated with consensus molecular subtypes 1 and 2
Chang, K., Willis, J. A., Reumers, J., Taggart, M. W., San Lucas, F. A., Thirumurthi, S., Kanth, P., Delker, D. A., Hagedorn, C. H., Lynch, P. M., et al. (2018) · Annals of Oncology · doi:10.1093/annonc/mdy337 · Cited by 51 · see citing works
BCL-XL is crucial for progression through the adenoma-to-carcinoma sequence of colorectal cancer
Ramesh, P., Lannagan, T. R. M., Jackstadt, R., Atencia Taboada, L., Lansu, N., Wirapati, P., van Hooff, S. R., Dekker, D., Pritchard, J., Kirov, A. B., et al. (2021) · Cell Death & Differentiation · doi:10.1038/s41418-021-00816-w · Cited by 52 · see citing works
Self-citationRecent Advances in CRISPR/Cas9 Delivery Approaches for Therapeutic Gene Editing of Stem Cells
Lotfi, M., Rad, D. M., Mashhadi, S., Ashouri, A., Mojarrad, M., Mozaffari‐Jovin, S., Farrokhi, S., Hashemi, M., Lotfi, M., Warkiani, M. E., et al. (2023) · Stem Cell Reviews and Reports · doi:10.1007/s12015-023-10585-3 · Cited by 54 · see citing works
Serrated Colorectal Cancer: The Road Less Travelled?
Nakanishi, Y., Díaz-Meco, M. T., & Moscat, J. (2019) · Trends in cancer · doi:10.1016/j.trecan.2019.09.004 · Cited by 51 · see citing works
Gastrointestinal cancer organoids—applications in basic and translational cancer research
Seidlitz, T., & Stange, D. E. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00654-3 · Cited by 49 · see citing works
Sessile serrated polyps and colon cancer prevention
Rashtak, S., Rego, R., Sweetser, S. R., & Sinicrope, F. A. (2017) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-16-0264 · Cited by 47 · see citing works
Sphyris, N., Hodder, M. C., & Sansom, O. J. (2021) · Cancers · doi:10.3390/cancers13051000 · Cited by 45 · see citing works
Mouillet-Richard, S., Cazelles, A., Sroussi, M., Gallois, C., Taieb, J., & Laurent-Puig, P. (2024) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-23-3964 · Cited by 43 · see citing works
Principles of Molecular Utility for CMS Classification in Colorectal Cancer Management
Rejali, L., Asl, R. S., Sanjabi, F., Fatemi, N., Aghdaei, H. A., Niasar, M. S., Moghadam, P. K., Mojarad, E. N., Mini, E., & Nobili, S. (2023) · Cancers · doi:10.3390/cancers15102746 · Cited by 45 · see citing works
Ullmann, P., Rodriguez, F., Schmitz, M., Meurer, S. K., Qureshi-Baig, K., Felten, P., Ginolhac, A., Antunes, L., Frasquilho, S., Zügel, N., et al. (2018) · Cancer Research · doi:10.1158/0008-5472.can-17-3003 · Cited by 43 · see citing works
Flum, M., Dicks, S., Teng, Y.-H., Schrempp, M., Nyström, A., Boerries, M., & Hecht, A. (2022) · Oncogene · doi:10.1038/s41388-022-02190-4 · Cited by 40 · see citing works
Trivieri, N., Pracella, R., Cariglia, M. G., Panebianco, C., Parrella, P., Visioli, A., Giani, F., Soriano, A. A., Barile, C., Canistro, G., et al. (2020) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-01801-w · Cited by 38 · see citing works
Muta, Y., Linares, J. F., Martínez-Ordóñez, A., Durán, Á., Cid-Diaz, T., Kinoshita, H., Zhang, X., Han, Q., Nakanishi, Y., Nakanishi, N., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43690-5 · Cited by 35 · see citing works
Sessile serrated lesions with dysplasia: is it possible to nip them in the bud?
Utsumi, T., Yamada, Y., Díaz-Meco, M. T., Moscat, J., & Nakanishi, Y. (2023) · Journal of Gastroenterology · doi:10.1007/s00535-023-02003-9 · Cited by 35 · see citing works
Baas, F. S., Brusselaers, N., Nagtegaal, I. D., Engstrand, L. G., & Boleij, A. (2024) · Cell Host & Microbe · doi:10.1016/j.chom.2024.07.008 · Cited by 32 · see citing works
Fu, Y., Guo, X., Sun, L., Cui, T., Wu, C., Wang, J., Liu, Y., & Liu, L. (2024) · eLife · doi:10.7554/elife.95009 · Cited by 31 · see citing works
Kim, J., Koo, B., & Yoon, K. (2019) · Viruses · doi:10.3390/v11020124 · Cited by 32 · see citing works
Intestinal multicellular organoids to study colorectal cancer
Idris, M., Alves, M. M., Hofstra, R. M. W., Mahé, M. M., & Melotte, V. (2021) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2021.188586 · Cited by 32 · see citing works
Ramakrishna, G., Babu, E., Singh, R., & Trehanpati, N. (2021) · Hepatology International · doi:10.1007/s12072-021-10237-z · Cited by 32 · see citing works
Ahuja, S., & Zaheer, S. (2023) · Cell Biology International · doi:10.1002/cbin.12097 · Cited by 32 · see citing works
Combinatorial Immunotherapies for Metastatic Colorectal Cancer
Janssen, E., Subtil, B., Ortiz, F. D. L. J., Verheul, H. M. W., & Tauriello, D. V. F. (2020) · Cancers · doi:10.3390/cancers12071875 · Cited by 30 · see citing works
Loss of primary cilia promotes inflammation and carcinogenesis
Paul, C., Tang, R., Longobardi, C., Lattanzio, R., Eguether, T., Turali, H., Bremond, J., Maurizy, C., Gabola, M., Poupeau, S., et al. (2022) · EMBO Reports · doi:10.15252/embr.202255687 · Cited by 30 · see citing works
Waehle, V., Ungricht, R., Hoppe, P. S., & Betschinger, J. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.07.023 · Cited by 27 · see citing works
Recent advances in understanding contextual TGFβ signaling
Ayyaz, A., Attisano, L., & Wrana, J. L. (2017) · F1000Research · doi:10.12688/f1000research.11295.1 · Cited by 26 · see citing works
Fibroblast Subsets in Intestinal Homeostasis, Carcinogenesis, Tumor Progression, and Metastasis
Dang, H., Harryvan, T. J., & Hawinkels, L. J. A. C. (2021) · Cancers · doi:10.3390/cancers13020183 · Cited by 26 · see citing works
Spheroids and organoids derived from colorectal cancer as tools for in vitro drug screening
Zawawi, S. S. A., Salleh, E. A., & Musa, M. (2024) · Exploration of Targeted Anti-tumor Therapy · doi:10.37349/etat.2024.00226 · Cited by 25 · see citing works
Razzaq, S., Fatima, I., Moafian, Z., Rahdar, A., Fathi‐karkan, S., Kharaba, Z. J., Shirzad, M., Khan, S. A., & Pandey, S. (2025) · Medical Oncology · doi:10.1007/s12032-025-02670-z · Cited by 26 · see citing works
Wang, Y., Hou, Q., Wu, Y., Xu, Y., Liu, Y., Chen, J., Xu, L., Guo, Y., Gao, S., & Yuan, J. (2021) · Animal nutrition · doi:10.1016/j.aninu.2021.06.001 · Cited by 25 · see citing works
Application Progress of Organoids in Colorectal Cancer
Luo, L., Ma, Y., Zheng, Y., Su, J., & Huang, G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.815067 · Cited by 25 · see citing works
Pentheroudakis, G. E., Mavroeidis, L., Papadopoulou, K., Koliou, G.-A., Bamia, C., Chatzopoulos, K., Samantas, E., Mauri, D. N., Efstratiou, I., Pectasides, D. G., et al. (2019) · Clinical Colorectal Cancer · doi:10.1016/j.clcc.2019.07.007 · Cited by 24 · see citing works
Wielandt, A. M., Hurtado, C., Mauricio Moreno, C., Villarroel, C., Castro, M., Estay, M., Simian, D., Martínez, M., Vial, M. T., Kronberg, U., et al. (2020) · Tumor Biology · doi:10.1177/1010428320938492 · Cited by 24 · see citing works
Serrated neoplasia in the colorectum: gut microbiota and molecular pathways
Kang, X., Zhang, R., Kwong, T. N. Y., Lui, R. N.-S., Wu, W. K. K., Sung, J. J. �., Yu, J. Q., & Wong, S. H. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1863135 · Cited by 23 · see citing works
Efficient genetic editing of human intestinal organoids using ribonucleoprotein-based CRISPR
Skoufou-Papoutsaki, N., Adler, S., D'Santos, P., Mannion, L., Mehmed, S., Kemp, R., Smith, A., Perrone, F., Nayak, K., Russell, A., et al. (2023) · Disease Models & Mechanisms · doi:10.1242/dmm.050279 · Cited by 22 · see citing works
Ding, X., Huang, H., Zhang, F., & Jiang, J. (2024) · Current Treatment Options in Oncology · doi:10.1007/s11864-024-01282-5 · Cited by 21 · see citing works
Organoids technology in cancer research: from basic applications to advanced ex vivo models
Varinelli, L., Illescas, O., Lorenc, E., Battistessa, D., Bella, M. D., Zanutto, S., & Gariboldi, M. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1569337 · Cited by 22 · see citing works
Wu, S., Tsai, W., Chiang, S.-F., Lai, Y.-H., Ma, C., Wang, J., Lin, J.-R., Lu, P.-S., Yang, C., Tan, B. C., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-61273-y · Cited by 21 · see citing works
Zhang, Y., Yang, Y., Qi, X., Cui, P., Kang, Y., Liu, H., Wei, Z., & Wang, H. (2024) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-024-03114-8 · Cited by 21 · see citing works
Yin, L., Zhou, S., Zhang, H., Shang, Y., Wu, S., & Jin, T. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1619597 · Cited by 18 · see citing works
Flanagan, D. J., Amirkhah, R., Vincent, D. F., Gündüz, N., Gentaz, P., Cammareri, P., McCooey, A. J., McCorry, A. M. B., Fisher, N. C., Belnoue-Davis, H. L., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35134-3 · Cited by 18 · see citing works
P�rez, A., Andrade‐Da‐Costa, J., de Souza, W. F., Ferreira, M. D. S., Boroni, M., de Oliveira, I. M., Freire‐Neto, C. A., Fernandes, P., Lanna, C. D., de Souza-Santos, P. T., et al. (2020) · Oncology Reports · doi:10.3892/or.2020.7727 · Cited by 18 · see citing works
From organoids to bedside: Advances in modeling, decoding and targeting of colorectal cancer
Betge, J., & Jackstadt, R. (2022) · International Journal of Cancer · doi:10.1002/ijc.34297 · Cited by 16 · see citing works
Huang, Y., Wang, G., Zhao, C., Geng, R., Zhang, S., Wang, W. T., Chen, J., Liu, H., & Wang, X. (2019) · Disease Markers · doi:10.1155/2019/5231269 · Cited by 17 · see citing works
Self-citationOrganoid Models for Cancer Research—From Bed to Bench Side and Back
Kastner, C., Hendricks, A., Deinlein, H., Hankir, M. K., Germer, C., Schmidt, S., & Wiegering, A. (2021) · Cancers · doi:10.3390/cancers13194812 · Cited by 17 · see citing works
Wu, Z.-H., Li, N., Gao, Z., Chen, G., Nie, L., Zhou, Y., Jiang, M.-Z., Chen, Y., Chen, J., Mei, X.-F., et al. (2022) · Cancers · doi:10.3390/cancers14194964 · Cited by 13 · see citing works
Kanth, P., Hazel, M. W., Boucher, K. M., Yang, Z., Wang, L., Bronner, M. P., Boylan, K. E., Burt, R. W., Westover, M., Neklason, D. W., et al. (2018) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22686 · Cited by 14 · see citing works
Kane, A. M., Fennell, L., Liu, C., Borowsky, J., McKeone, D., Bond, C., Kazakoff, S. H., Patch, A., Koufariotis, L. T., Pearson, J. V., et al. (2020) · Neoplasia · doi:10.1016/j.neo.2019.12.002 · Cited by 14 · see citing works
Modeling epithelial-mesenchymal transition in patient-derived breast cancer organoids
Bar-Hai, N., Ben-Yishay, R., Arbili-Yarhi, S., Herman, N., Noy, V., Menes, T. S., Mansour, A., Awwad, F., Balint‐Lahat, N., Goldinger, G., et al. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1470379 · Cited by 13 · see citing works
- Authors
- Fessler, E., Drost, J., van Hooff, S. R., Linnekamp, J. F., Wang, X., Jansen, M., De Sousa E Melo, F., Prasetyanti, P. R., IJspeert, J. E., Franitza, M., Nürnberg, P., van Noesel, C. J., Dekker, E., Vermeulen, L., Clevers, H., & Medema, J. P.
- Affiliations
- Amsterdam UMC Location University of Amsterdam (NL)
- Royal Netherlands Academy of Arts and Sciences (NL)
- City University of Hong Kong (HK)
- University of Cologne (DE)
- Corresponding author
- Medema, Jan Paul
- ORCID
- Venue
- EMBO Molecular Medicine
- Published
- 2016-05-24
- Volume
- 8
- Issue
- 7
- Pages
- 745-760
- ISSN
- 1757-4676 (ISSN-L)
- 1757-4684
- PMC
- PMC4931289
- OpenAlex
- W2404590196
- Cited by
- 159
- References
- 69
- Citations by year
- 2026: 7 · 2025: 15 · 2024: 16 · 2023: 12 · 2022: 16 · 2021: 20 · 2020: 25 · 2019: 13 · 2018: 16 · 2017: 14 · 2016: 4
- FWCI
- 8.14
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- EMBO Molecular Medicine (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion, other-oa)
- KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (publishedVersion, other-oa)
- KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (publishedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- UCL Discovery (University College London) (submittedVersion)
- CityU Scholars (submittedVersion, cc-by)
- Funders
- AMC Graduate School PhD Scholarship
- NWO‐ZonMw VENI (91614138)
- Dutch Cancer Society (UvA2013‐6331, UvA2014‐7245, UvA2015‐7587)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Keywords
- TGF-beta signaling, colorectal cancer, consensus molecular subtypes, CMS4, mesenchymal subtype, sessile serrated adenoma, serrated neoplasia, tubular adenoma, BRAF V600E mutation, colorectal organoids, apoptosis, tumor progression, precursor lesions
- MeSH terms
- Adenoma, Humans, Organoids, Colorectal Neoplasms, Signal Transduction, Transforming Growth Factor beta, Carcinogenesis
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