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WNT as a Driver and Dependency in Cancer
Open accessAbstract
The WNT signaling pathway is a critical regulator of development and adult tissue homeostasis and becomes dysregulated in many cancer types. Although hyperactivation of WNT signaling is common, the type and frequency of genetic WNT pathway alterations can vary dramatically between different cancers, highlighting possible cancer-specific mechanisms for WNT-driven disease. In this review, we discuss how WNT pathway disruption contributes to tumorigenesis in different organs and how WNT affects the tumor cell and immune microenvironment. Finally, we describe recent and ongoing efforts to target oncogenic WNT signaling as a therapeutic strategy. Significance: WNT signaling is a fundamental regulator of tissue homeostasis and oncogenic driver in many cancer types. In this review, we highlight recent advances in our understanding of WNT signaling in cancer, particularly the complexities of WNT activation in distinct cancer types, its role in immune evasion, and the challenge of targeting the WNT pathway as a therapeutic strategy.
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“The Wnt/β-catenin pathway also plays a critical role in maintaining the cancer stem cell (CSC) population in malignant tissues making Wnt a potential target in CRC [109]”
From Recent Advances in Therapeutic Strategies to Improve Colorectal Cancer Treatment (2024) · cites this paper as [109]
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Cites
Comprehensive molecular characterization of human colon and rectal cancer
The Cancer Genome Atlas Network (2012) · Nature · doi:10.1038/nature11252 · Cited by 8,499
Identification of stem cells in small intestine and colon by marker gene Lgr5
Barker, N., van Es, J. H., Kuipers, J., Kujala, P., van den Born, M., Cozijnsen, M., Haegebarth, A., Korving, J., Begthel, H., Peters, P. J., et al. (2007) · Nature · doi:10.1038/nature06196 · Cited by 5,687
Wnt/β-catenin signaling and disease
Clevers, H., & Nusse, R. (2012) · Cell · doi:10.1016/j.cell.2012.05.012 · Cited by 5,554
Cancer Metastasis: Building a Framework
Gupta, G. P., & Massagué, J. (2006) · Cell · doi:10.1016/j.cell.2006.11.001 · Cited by 4,333
Wnt signalling in stem cells and cancer
Reya, T., & Clevers, H. (2005) · Nature · doi:10.1038/nature03319 · Cited by 3,666
Melanoma-intrinsic β-catenin signalling prevents anti-tumour immunity
Spranger, S., Bao, R., & Gajewski, T. F. (2015) · Nature · doi:10.1038/nature14404 · Cited by 2,830
Identification and characterization of the familial adenomatous polyposis coli gene
Groden, J. L., Thliveris, A. T., Samowitz, W. S., Carlson, M. L., Gelbert, L. M., Albertsen, H., Joslyn, G., Stevens, J., Spirio, L. N., Robertson, M. A., et al. (1991) · Cell · doi:10.1016/0092-8674(81)90021-0 · Cited by 2,794
Zhan, T., Rindtorff, N., & Boutros, M. (2017) · Oncogene · doi:10.1038/onc.2016.304 · Cited by 2,626
Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts
Sato, T., van Es, J. H., Snippert, H. J., Stange, D. E., Vries, R. G., van den Born, M., Barker, N., Shroyer, N. F., van de Wetering, M., & Clevers, H. (2011) · Nature · doi:10.1038/nature09637 · Cited by 2,510
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
Crypt stem cells as the cells-of-origin of intestinal cancer
Barker, N., Ridgway, R. A., van Es, J. H., van de Wetering, M., Begthel, H., van den Born, M., Danenberg, E., Clarke, A. R., Sansom, O. J., & Clevers, H. C. (2008) · Nature · doi:10.1038/nature07602 · Cited by 2,232
WNT signalling pathways as therapeutic targets in cancer
Anastas, J. N., & Moon, R. T. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3419 · Cited by 1,945
Nusse, R., & VARMUS, H. E. (1982) · Cell · doi:10.1016/0092-8674(82)90409-3 · Cited by 1,864
The many faces and functions of β‐catenin
Valenta, T., Hausmann, G., & Basler, K. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.150 · Cited by 1,598
Canonical wnt signaling in differentiated osteoblasts controls osteoclast differentiation.
Glass, D. A., Bialek, P., Ahn, J. D., Starbuck, M., Patel, M. S., Clevers, H., Taketo, M. M., Long, F., McMahon, A. P., Lang, R. A., et al. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.02.017 · Cited by 1,558
Multiple Intestinal Neoplasia Caused by a Mutation in the Murine Homolog of the APC Gene
Su, L.-K., Kinzler, K. W., Vogelstein, B., Preisinger, A. C., Moser, A. R., Luongo, C., Gould, K. A., & Dove, W. F. (1992) · Science · doi:10.1126/science.1350108 · Cited by 1,537
Guichard, C., Amaddeo, G., Imbeaud, S., Ladeiro, Y., Pelletier, L., Benmaad, I., Caldéraro, J., Bioulac‐Sage, P., Letexier, M., Degos, F., et al. (2012) · Nature Genetics · doi:10.1038/ng.2256 · Cited by 1,522
An integral program for tissue renewal and regeneration: Wnt signaling and stem cell control
Clevers, H. C., Loh, K. M., & Nusse, R. (2014) · Science · doi:10.1126/science.1248012 · Cited by 1,386
Lgr5 homologues associate with Wnt receptors and mediate R-spondin signalling
de Lau, W., Barker, N., Low, T. Y., Koo, B., Li, V. S. W., Teunissen, H., Kujala, P., Haegebarth, A., Peters, P. J., van de Wetering, M., et al. (2011) · Nature · doi:10.1038/nature10337 · Cited by 1,302
Intestinal polyposis in mice with a dominant stable mutation of the β‐catenin gene
Harada, N., Tamai, Y., Ishikawa, T., Sauer, B., Takaku, K., Oshima, M., & Taketo, M. M. (1999) · The EMBO Journal · doi:10.1093/emboj/18.21.5931 · Cited by 1,212
Ku, S., Rosario, S. R., Wang, Y., Mu, P., Seshadri, M., Goodrich, Z., Goodrich, M. M., Labbé, D. P., Gomez, E. C., Wang, J., et al. (2017) · Science · doi:10.1126/science.aah4199 · Cited by 1,117
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 1,110
Intestinal Tumorigenesis Initiated by Dedifferentiation and Acquisition of Stem-Cell-like Properties
Schwitalla, S., Fingerle, A. A., Cammareri, P., Nebelsiek, T., Göktuna, S. İ., Ziegler, P. K., Canli, Ö., Heijmans, J., Huels, D. J., Moreaux, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.12.012 · Cited by 1,098
YAP/TAZ incorporation in the β-catenin destruction complex orchestrates the Wnt response
Azzolin, L., Panciera, T., Soligo, S., Enzo, E., Bicciato, S., Dupont, S., Bresolin, S., Frasson, C., Basso, G., Guzzardo, V., et al. (2014) · Cell · doi:10.1016/j.cell.2014.06.013 · Cited by 1,094
Mu, P., Zhang, Z., Benelli, M., Karthaus, W. R., Hoover, E., Chen, C.-C., Wongvipat, J., Ku, S., Gao, D., Cao, Z., et al. (2017) · Science · doi:10.1126/science.aah4307 · Cited by 1,089
Kato, M., Patel, M. S., Levasseur, R., Lobov, I., Chang, B. H.-J., Glass, D. A., Hartmann, C., Li, L., Hwang, T.-H., Brayton, C. F., et al. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200201089 · Cited by 1,086
Wnt-dependent de novo hair follicle regeneration in adult mouse skin after wounding
Ito, M., Yang, Z., Andl, T., Cui, C., Kim, N., Millar, S. E., & Cotsarelis, G. (2007) · Nature · doi:10.1038/nature05766 · Cited by 1,064
Tales from the crypt: new insights into intestinal stem cells
Gehart, H., & Clevers, H. C. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-018-0081-y · Cited by 1,046
Kremen proteins are Dickkopf receptors that regulate Wnt/β-catenin signalling
Mao, B., Wu, W., Davidson, G., Marhold, J., Li, M., Mechler, B. M., Delius, H., Hoppe, D., Stannek, P., Walter, C., et al. (2002) · Nature · doi:10.1038/nature756 · Cited by 1,038
Tumour suppressor RNF43 is a stem-cell E3 ligase that induces endocytosis of Wnt receptors
Koo, B.-K., Spit, M., Jordens, I., Low, T. Y., Stange, D. E., van de Wetering, M., van Es, J. H., Mohammed, S., Heck, A. J. R., Maurice, M. M., et al. (2012) · Nature · doi:10.1038/nature11308 · Cited by 980
ZNRF3 promotes Wnt receptor turnover in an R-spondin-sensitive manner
Hao, H.-X., Xie, Y., Zhang, Y., Charlat, O., Oster, E., Avello, M., Lei, H., Mickanin, C., Liu, D., Ruffner, H., et al. (2012) · Nature · doi:10.1038/nature11019 · Cited by 962
Recurrent R-spondin fusions in colon cancer
Seshagiri, S., Stawiski, E. W., Durinck, S., Modrusan, Z., Storm, E. E., Conboy, C. B., Chaudhuri, S., Guan, Y., Janakiraman, V., Jaiswal, B. S., et al. (2012) · Nature · doi:10.1038/nature11282 · Cited by 960
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
Ruiz de Galarreta, M., Bresnahan, E., Molina-Sánchez, P., Lindblad, K. E., Maier, B., Sia, D., Puigvehi, M., Miguela, V., Casanova-Acebes, M., Dhainaut, M., et al. (2019) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-0074 · Cited by 912
Carmon, K. S., Gong, X. W., Lin, Q., Thomas, A., & Liu, Q. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106083108 · Cited by 894
Hogan, B. L. M., Barkauskas, C. E., Chapman, H. A., Epstein, J. A., Jain, R., Hsia, C. C. W., Niklason, L., Calle, E., Le, A., Randell, S. H., et al. (2014) · Cell Stem Cell · doi:10.1016/j.stem.2014.07.012 · Cited by 876
Paracrine and Autocrine Signals Induce and Maintain Mesenchymal and Stem Cell States in the Breast
Scheel, C., Eaton, E. N., Li, H., Chaffer, C. L., Reinhardt, F., Kah, K.-J., Bell, G. W., Guo, W., Rubin, J. S., Richardson, A. L., et al. (2011) · Cell · doi:10.1016/j.cell.2011.04.029 · Cited by 859
Clinical Sequencing Defines the Genomic Landscape of Metastatic Colorectal Cancer
Yaeger, R., Chatila, W. K., Lipsyc, M. D., Hechtman, J. F., Cercek, A., Sanchez-Vega, F., Jayakumaran, G., Middha, S., Zehir, A., Donoghue, M. T. A., et al. (2018) · Cancer Cell · doi:10.1016/j.ccell.2017.12.004 · Cited by 858
Targeting Wnt-driven cancer through the inhibition of Porcupine by LGK974
Liu, J., Pan, S., Hsieh, M. H., Ng, N., Sun, F., Wang, T., Kasibhatla, S., Schuller, A. G., Li, A. G., Cheng, D., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1314239110 · Cited by 851
Loss of Apc in vivo immediately perturbs Wnt signaling, differentiation, and migrationPreprint
Sansom, O. J., Reed, K. R., Hayes, A. J., Ireland, H., Brinkmann, H., Newton, I. P., Batlle, E., Simon-Assmann, P. M., Clevers, H. C., Näthke, I. S., et al. (2004) · Genes & Development · doi:10.1101/gad.287404 · Cited by 824
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 812
Monounsaturated Fatty Acid Modification of Wnt Protein: Its Role in Wnt Secretion
Takada, R., Satomi, Y., Kurata, T., Ueno, N., Norioka, S., Kondoh, H., Takao, T., & Takada, S. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.10.003 · Cited by 809
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
Familial adenomatous polyposis
Galiatsatos, P., & Foulkes, W. D. (2006) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2006.00375.x · Cited by 757
Boulter, L., Govaere, O., Bird, T. G., Radulescu, S., Ramachandran, P., Pellicoro, A., Ridgway, R. A., Seo, S. S., Spee, B., Van Rooijen, N., et al. (2012) · Nature Medicine · doi:10.1038/nm.2667 · Cited by 747
Visualization and targeting of LGR5+ human colon cancer stem cells
Shimokawa, M., Ohta, Y., Nishikori, S., Matano, M., Takano, A., Fujii, M., Date, S., Sugimoto, S., Kanai, T., & Sato, T. (2017) · Nature · doi:10.1038/nature22081 · Cited by 728
Unlimited in vitro expansion of adult bi‐potent pancreas progenitors through the Lgr5/R‐spondin axis
Huch, M., Bonfanti, P., Boj, S. F., Sato, T., Loomans, C. J. M., van de Wetering, M., Sojoodi, M., Li, V. S. W., Schuijers, J., Gracanin, A., et al. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.204 · Cited by 726
WNT/β-catenin pathway activation correlates with immune exclusion across human cancers
Luke, J. J., Bao, R., Sweis, R. F., Spranger, S., & Gajewski, T. F. (2019) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-18-1942 · Cited by 722
YAP/TAZ-Dependent Reprogramming of Colonic Epithelium Links ECM Remodeling to Tissue Regeneration
Yui, S., Azzolin, L., Maimets, M., Pedersen, M. T., Fordham, R. P., Hansen, S. L., Larsen, H. L., Guiu, J., Alves, M. R. P., Rundsten, C. F., et al. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.11.001 · Cited by 678
Wnt Signaling Pathway in Non-Small Cell Lung Cancer
Stewart, D. J. (2013) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djt356 · Cited by 653
RB loss in resistant EGFR mutant lung adenocarcinomas that transform to small-cell lung cancer
Niederst, M. J., Sequist, L. V., Poirier, J. T., Mermel, C. H., Lockerman, E. L., Garcia, A. R., Katayama, R., Costa, C., Ross, K. N., Moran, T., et al. (2015) · Nature Communications · doi:10.1038/ncomms7377 · Cited by 647
Secreted and transmembrane wnt inhibitors and activators
Cruciat, C.-M., & Niehrs, C. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a015081 · Cited by 646
To differentiate or not — routes towards metastasis
Brabletz, T. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3265 · Cited by 638
Seino, T., Kawasaki, S., Shimokawa, M., Tamagawa, H., Toshimitsu, K., Fujii, M., Ohta, Y., Matano, M., Nanki, K., Kawasaki, K., et al. (2018) · Cell Stem Cell · doi:10.1016/j.stem.2017.12.009 · Cited by 631
Gurney, A., Axelrod, F., Bond, C. J., Cain, J., Chartier, C., Donigan, L., Fischer, M., Chaudhari, A., Ji, M., Kapoun, A. M., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120068109 · Cited by 614
Lung development: orchestrating the generation and regeneration of a complex organ
Herriges, M., & Morrisey, E. E. (2014) · Development · doi:10.1242/dev.098186 · Cited by 613
Haigis, K. M., Kendall, K. R., Wang, Y., Cheung, A., Haigis, M. C., Glickman, J. N., Niwa-Kawakita, M., Sweet-Cordero, A., Sebolt-Leopold, J., Shannon, K. M., et al. (2008) · Nature Genetics · doi:10.1038/ng.115 · Cited by 610
Single-cell transcriptomes of the regenerating intestine reveal a revival stem cell
Ayyaz, A., Kumar, S., Sangiorgi, B., Ghoshal, B., Gosio, J., Ouladan, S., Fink, M., Barutcu, S., Trcka, D., Shen, J., et al. (2019) · Nature · doi:10.1038/s41586-019-1154-y · Cited by 593
WNT signalling in the immune system: WNT is spreading its wings
Staal, F. J. T., Luis, T. C., & Tiemessen, M. M. (2008) · Nature Reviews Immunology · doi:10.1038/nri2360 · Cited by 582
Dow, L. E., O’Rourke, K. P., Simon, J. M., Tschaharganeh, D. F., van Es, J. H., Clevers, H. C., & Lowe, S. W. (2015) · Cell · doi:10.1016/j.cell.2015.05.033 · Cited by 569
Self-citationGenetic Mechanisms of Immune Evasion in Colorectal Cancer
Grasso, C. S., Giannakis, M., Wells, D. K., Hamada, T., Mu, X. J., Quist, M., Nowak, J. A., Nishihara, R., Qian, Z. R., Inamura, K., et al. (2018) · Cancer Discovery · doi:10.1158/2159-8290.cd-17-1327 · Cited by 535
Subepithelial telocytes are an important source of Wnts that supports intestinal crypts
Shoshkes-Carmel, M., Wang, Y. J., Wangensteen, K. J., Tóth, B., Kondo, A., Massasa, E. E., Itzkovitz, S., & Kaestner, K. H. (2018) · Nature · doi:10.1038/s41586-018-0084-4 · Cited by 525
RNF43 is frequently mutated in colorectal and endometrial cancers
Giannakis, M., Hodis, E., Mu, X. J., Yamauchi, M., Rosenbluh, J., Cibulskis, K., Saksena, G., Lawrence, M. S., Qian, Z. R., Nishihara, R., et al. (2014) · Nature Genetics · doi:10.1038/ng.3127 · Cited by 490
Small-molecule inhibition of Wnt signaling through activation of casein kinase 1α
Thorne, C. A., Hanson, A. J., Schneider, J., Tahinci, E., Orton, D., Cselenyi, C. S., Jernigan, K. K., Meyers, K. C., Hang, B. I., Waterson, A. G., et al. (2010) · Nature Chemical Biology · doi:10.1038/nchembio.453 · Cited by 485
Näthke, I. S., Adams, C. L., Polakis, P. G., Sellin, J. H., & Nelson, W. J. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.134.1.165 · Cited by 484
Kurayoshi, M., Oue, N., Yamamoto, H., Kishida, M., Inoue, A., Asahara, T., Yasui, W., & Kikuchi, A. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-2359 · Cited by 453
Baker, N. E. (1987) · The EMBO Journal · doi:10.1002/j.1460-2075.1987.tb02429.x · Cited by 436
Inactivating mutations of RNF43 confer Wnt dependency in pancreatic ductal adenocarcinoma
Jiang, X., Hao, H.-X., Growney, J. D., Woolfenden, S., Bottiglio, C., Ng, N., Lu, B., Hsieh, M. H., Bagdasarian, L., Meyer, R., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307218110 · Cited by 415
Defining the impact of β-catenin/Tcf transactivation on epithelial stem cellsPreprint
Lowry, W. E., Blanpain, C., Nowak, J. A., Guasch, G., Lewis, L. E., & Fuchs, E. V. (2005) · Genes & Development · doi:10.1101/gad.1324905 · Cited by 402
Long-lived intestinal tuft cells serve as colon cancer–initiating cells
Westphalen, C. B., Asfaha, S., Hayakawa, Y., Takemoto, Y., Lukin, D. J., Nuber, A. H., Brandtner, A. K., Setlik, W., Remotti, H. E., Muley, A., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci73434 · Cited by 400
Koch, A., Denkhaus, D., Albrecht, S., Leuschner, I., von Schweinitz, D., & Pietsch, T. (1999) · PubMed · Cited by 399
Albuquerque, C. M. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.13.1549 · Cited by 392
Wnt signaling in adult intestinal stem cells and cancer
Krausová, M., & Kořínek, V. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.11.032 · Cited by 380
Stroma provides an intestinal stem cell niche in the absence of epithelial Wnts
Kabiri, Z., Greicius, G., Madan, B., Biechele, S., Zhong, Z. A., Zaribafzadeh, H., Edison, Aliyev, J., Wu, Y., Bunte, R. M., et al. (2014) · Development · doi:10.1242/dev.104976 · Cited by 351
Colnot, S., Decaens, T., Niwa‐Kawakita, M., Godard, C., Hamard, G., Kahn, A., Giovannini, M., & Perret, C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0404761101 · Cited by 346
Wnt addiction of genetically defined cancers reversed by PORCN inhibition
Madan, B., Ke, Z., Harmston, N., Ho, S. Y., Frois, A. O., Alam, J., Jeyaraj, D. A., Pendharkar, V. V., Ghosh, K., Virshup, I., et al. (2015) · Oncogene · doi:10.1038/onc.2015.280 · Cited by 343
Gonsalves, F. C., Klein, K., Carson, B. B., Katz, S., Ekas, L. A., Evans, S., Nagourney, R., Cardozo, T., Brown, A. M. C., & DasGupta, R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1017496108 · Cited by 337
Plasticity of Lgr5-Negative Cancer Cells Drives Metastasis in Colorectal Cancer
Fumagalli, A., Oost, K. C., Kester, L. A., Morgner, J., Bornes, L., Bruens, L., Spaargaren, L., Azkanaz, M., Schelfhorst, T., Beerling, E., et al. (2020) · Cell stem cell · doi:10.1016/j.stem.2020.02.008 · Cited by 336
A Wnt-producing niche drives proliferative potential and progression in lung adenocarcinoma
Tammela, T., Rivera, F. J. S., Cetinbas, N. M., Wu, K., Joshi, N. S., Helenius, K., Park, Y., Azimi, R., Kerper, N. R., Wesselhoeft, R. A., et al. (2017) · Nature · doi:10.1038/nature22334 · Cited by 335
Self-citationA Novel Tankyrase Small-Molecule Inhibitor Suppresses APC Mutation–Driven Colorectal Tumor Growth
Lau, T., Chan, E., Callow, M., Waaler, J., Boggs, J., Blake, R. A., Magnuson, S., Sambrone, A., Schutten, M., Firestein, R., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-4562 · Cited by 316
Lachenmayer, A., Alsinet, C., Savic, R., Cabellos, L., Toffanin, S., Hoshida, Y., Villanueva, A., Minguez, B., Newell, P., Tsai, H.-W., et al. (2012) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-11-2322 · Cited by 306
Wnt Pathway in Bone Repair and Regeneration – What Do We Know So Far
Houschyar, K. S., Tapking, C., Borrelli, M. R., Popp, D., Duscher, D., Maan, Z. N., Chelliah, M. P., Li, J., Harati, K., Wallner, C., et al. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00170 · Cited by 306
Letouzé, É., Shinde, J., Renault, V., Couchy, G., Blanc, J., Tubacher, E., Bayard, Q., Bacq, D., Meyer, V., Semhoun, J., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01358-x · Cited by 303
Mustata, R. C., Vasile, G., Vallone, V. B. F., Strollo, S., Lefort, A., Libert, F., Monteyne, D., Pérez-Morga, D. L., Vassart, G., & Garcia, M. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.09.005 · Cited by 292
Greicius, G., Kabiri, Z., Sigmundsson, K., Liang, C., Bunte, R., Singh, M. K., & Virshup, D. M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1713510115 · Cited by 286
A Gata6-Wnt pathway required for epithelial stem cell development and airway regeneration
Zhang, Y., Goss, A., Cohen, E. D., Kadzik, R. S., Lepore, J. J., Muthukumaraswamy, K., Yang, J., DeMayo, F. J., Whitsett, J. A., Parmacek, M. S., et al. (2008) · Nature Genetics · doi:10.1038/ng.157 · Cited by 284
The genomic landscape of hepatoblastoma and their progenies with HCC-like features
Eichenmüller, M., Trippel, F., Kreuder, M., Beck, A., Schwarzmayr, T., Häberle, B., Cairo, S., Leuschner, I., von Schweinitz, D., Strom, T. M., et al. (2014) · Journal of Hepatology · doi:10.1016/j.jhep.2014.08.009 · Cited by 258
Targeting PTPRK-RSPO3 colon tumours promotes differentiation and loss of stem-cell function
Storm, E. E., Durinck, S., Melo, F. D. S. E., Tremayne, J. R., Kljavin, N. M., Tan, C., Ye, X., Chiu, C., Pham, T., Hongo, J.-A., et al. (2015) · Nature · doi:10.1038/nature16466 · Cited by 246
O’Rourke, K. P., Loizou, E., Livshits, G., Schatoff, E. M., Baslan, T., Manchado, E., Simon, J. M., Romesser, P. B., Leach, B. I., Han, T., et al. (2017) · Nature Biotechnology · doi:10.1038/nbt.3837 · Cited by 244
Self-citationSpindle Orientation Bias in Gut Epithelial Stem Cell Compartments Is Lost in Precancerous Tissue
Quyn, A. J., Appleton, P. L., Carey, F. A., Steele, R. J. C., Barker, N., Clevers, H., Ridgway, R. A., Sansom, O. J., & Näthke, I. S. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2009.12.007 · Cited by 242
An Organoid Biobank of Neuroendocrine Neoplasms Enables Genotype-Phenotype Mapping
Kawasaki, K., Toshimitsu, K., Matano, M., Fujita, M., Fujii, M., Togasaki, K., Ebisudani, T., Shimokawa, M., Takano, A., Takahashi, S., et al. (2020) · Cell · doi:10.1016/j.cell.2020.10.023 · Cited by 238
Wnt/Planar cell polarity signaling: A new paradigm for cancer therapy
Wang, Y. (2009) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-09-0282 · Cited by 216
Common dysregulation of Wnt/Frizzled receptor elements in human hepatocellular carcinoma
Bengochea, A., de Souza, M. M., Lefrançois, L., Le Roux, E., Galy, O., Chemin, I., Kim, M., Wands, J. R., Trepo, C., Hainaut, P., et al. (2008) · British Journal of Cancer · doi:10.1038/sj.bjc.6604422 · Cited by 215
HOXA5 Counteracts Stem Cell Traits by Inhibiting Wnt Signaling in Colorectal Cancer
Ordóñez-Morán, P., Dafflon, C., Imajo, M., Nishida, E., & Huelsken, J. (2015) · Cancer Cell · doi:10.1016/j.ccell.2015.11.001 · Cited by 209
Tankyrase Inhibitors Target YAP by Stabilizing Angiomotin Family Proteins
Wang, W., Li, N., Li, X., Tran, M. K., Han, X., & Chen, J. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.014 · Cited by 209
EPITHELIAL CELL MIGRATION IN THE INTESTINE
Heath, J. P. (1996) · Cell Biology International · doi:10.1006/cbir.1996.0018 · Cited by 205
Ding, Y., Shen, S., Lino, A. C., de Lafaille, M. A. C., & Lafaille, J. J. (2008) · Nature Medicine · doi:10.1038/nm1707 · Cited by 204
Death in the intestinal epithelium—basic biology and implications for inflammatory bowel disease
Blander, J. M. (2016) · FEBS Journal · doi:10.1111/febs.13771 · Cited by 197
Oncogenic Kras drives invasion and maintains metastases in colorectal cancer
Boutin, A. T., Liao, W.-T., Wang, M., Hwang, S. S., Karpinets, T. V., Cheung, H., Chu, G. C., Jiang, S., Hu, J., Chang, K., et al. (2017) · Genes & Development · doi:10.1101/gad.293449.116 · Cited by 195
Wnt/Beta-Catenin Signaling Regulation and a Role for Biomolecular Condensates
Schaefer, K. N., & Peifer, M. A. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.01.025 · Cited by 195
Role of Oncogenic K-Ras in Cancer Stem Cell Activation by Aberrant Wnt/β-Catenin Signaling
Moon, B.-S., Jeong, W.-J., Park, J., Kim, T. I., Min, D. S., & Choi, K. (2014) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djt373 · Cited by 189
MEK inhibitors activate Wnt signalling and induce stem cell plasticity in colorectal cancer
Zhan, T., Ambrosi, G., Wandmacher, A. M., Rauscher, B., Betge, J., Rindtorff, N., Häussler, R. S., Hinsenkamp, I., Bamberg, L., Hessling, B., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09898-0 · Cited by 189
Talbot, L. J., Bhattacharya, S. D., & Kuo, P. C. (2012) · Europe PMC (PubMed Central) · Cited by 176
Yaguchi, T., Goto, Y., Kido, K., Mochimaru, H., Sakurai, T., Tsukamoto, N., Kudo‐Saito, C., Fujita, T., Sumimoto, H., & Kawakami, Y. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102282 · Cited by 169
Christie, M., Jorissen, R. N., Mouradov, D., Sakthianandeswaren, A., Li, S., Day, F. L., Tsui, C. S., Lipton, L. R., Desai, J., Jones, I. T., et al. (2012) · Oncogene · doi:10.1038/onc.2012.486 · Cited by 168
Hepatoblastoma and APC gene mutation in familial adenomatous polyposis.
Giardiello, F. M., Petersen, G. M., Brensinger, J. D., Luce, M. C., Cayouette, M. C., Bacon, J. A., Booker, S. V., & Hamilton, S. R. (1996) · Gut · doi:10.1136/gut.39.6.867 · Cited by 168
Histone methyltransferase SETD2 modulates alternative splicing to inhibit intestinal tumorigenesis
Yuan, H., Li, N., Fu, D., Ren, J., Hui, J., Peng, J., Liu, Y., Qiu, T., Jiang, M., Pan‐Hammarström, Q., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci94292 · Cited by 165
Gang, E. J., Hsieh, Y.-T., Pham, J., Zhao, Y., Nguyen, C., Huantes, S., Park, E., Naing, K. W., Klemm, L., Swaminathan, S., et al. (2013) · Oncogene · doi:10.1038/onc.2013.169 · Cited by 164
Pacheco-Pinedo, E. C., Durham, A. C., Stewart, K. M., Goss, A. M., Lu, M. M., DeMayo, F. J., & Morrisey, E. E. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44871 · Cited by 164
Nejak-Bowen, K., Thompson, M. D., Singh, S., Bowen, W., Dar, M. J., Khillan, J., Dai, C.-S., & Monga, S. P. S. (2010) · Hepatology · doi:10.1002/hep.23538 · Cited by 160
Porcupine inhibitor suppresses paracrine Wnt-driven growth of Rnf43;Znrf3 -mutant neoplasia
Koo, B., van Es, J. H., van den Born, M., & Clevers, H. C. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508113112 · Cited by 157
Tam, B. Y. Y., Chiu, K., Chung, H., Bossard, C., Nguyen, J. D., Creger, E., Eastman, B. W., Mak, C. C., Ibanez, M., Ghias, A., et al. (2019) · Cancer Letters · doi:10.1016/j.canlet.2019.09.009 · Cited by 154
Eyre, R., Alférez, D., Santiago-Gómez, A., Spence, K., McConnell, J. C., Hart, C. A., Simões, B. M., Lefley, D. V., Tulotta, C., Storer, J. A., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12807-0 · Cited by 150
Frequent PTPRK–RSPO3 fusions and RNF43 mutations in colorectal traditional serrated adenoma
Sekine, S., Yamashita, S., Tanabe, T., Hashimoto, T., Yoshida, H., Taniguchi, H., Kojima, M., Shinmura, K., Saito, Y., Hiraoka, N., et al. (2016) · The Journal of Pathology · doi:10.1002/path.4709 · Cited by 146
Cell regulation by the Apc protein
McCartney, B. M., & Näthke, I. S. (2008) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2008.02.001 · Cited by 144
Wnt Signaling, Stem Cells, and Cancer of the Gastrointestinal TractPreprint
Schepers, A. G., & Clevers, H. C. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a007989 · Cited by 140
Faux, M. C., Ross, J., Meeker, C. T., Johns, T. G., Ji, H. L., Simpson, R. J., Layton, M. J., & Burgess, A. W. (2003) · Journal of Cell Science · doi:10.1242/jcs.00862 · Cited by 136
Epigenetic alteration of Wnt pathway antagonists in progressive glandular neoplasia of the lung
Licchesi, J. D. F., Westra, W. H., Hooker, C. M., Machida, E. O., Baylin, S. B., & Herman, J. G. (2008) · Carcinogenesis · doi:10.1093/carcin/bgn017 · Cited by 129
JUNB governs a feed-forward network of TGFβ signaling that aggravates breast cancer invasion
Sundqvist, A., Morikawa, M., Ren, J., Vasilaki, E., Kawasaki, N., Kobayashi, M., Koinuma, D., Aburatani, H., Miyazono, K., Heldin, C., et al. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx1190 · Cited by 128
Non-traditional roles for the Adenomatous Polyposis Coli (APC) tumor suppressor protein
Hanson, C. A., & Miller, J. R. (2005) · Gene · doi:10.1016/j.gene.2005.07.024 · Cited by 126
Mapping the in vivo fitness landscape of lung adenocarcinoma tumor suppression in mice
Rogers, Z. N., McFarland, C. D., Winters, I. P., Seoane, J. A., Brady Jennifer, J., Yoon, S. M., Curtis, C. N., Petrov, D. A., & Winslow, M. M. (2018) · Nature Genetics · doi:10.1038/s41588-018-0083-2 · Cited by 125
Yuan, H., Manoharan, I., Suryawanshi, A. S., Majumdar, T., Angus-Hill, M. L., Koni, P. A., Manicassamy, B., Mellor, A. L., Munn, D. H., & Manicassamy, S. (2015) · Cancer Research · doi:10.1158/0008-5472.can-14-2377 · Cited by 123
Han, T., Schatoff, E. M., Murphy, C. J., Zafra, M. P., Wilkinson, J. E., Elemento, O., & Dow, L. E. (2017) · Nature Communications · doi:10.1038/ncomms15945 · Cited by 117
Self-citationWnt signaling suppresses MAPK-driven proliferation of intestinal stem cells
Kabiri, Z., Greicius, G., Zaribafzadeh, H., Hemmerich, A. C., Counter, C. M., & Virshup, D. M. (2018) · Journal of Clinical Investigation · doi:10.1172/jci99325 · Cited by 117
Abitbol, S., Dahmani, R., Coulouarn, C., Ragazzon, B., Mlecnik, B., Senni, N., Savall, M., Bossard, P., Sohier, P., Drouet, V., et al. (2018) · Journal of Hepatology · doi:10.1016/j.jhep.2017.12.018 · Cited by 117
Molina-Sánchez, P., Ruiz de Galarreta, M., Yao, M. A., Lindblad, K. E., Bresnahan, E., Bitterman, E., Martin, T. C., Rubenstein, T., Nie, K., Golas, J., et al. (2020) · Gastroenterology · doi:10.1053/j.gastro.2020.08.015 · Cited by 117
The effects of mutational processes and selection on driver mutations across cancer types
Temko, D., Tomlinson, I. P. M., Severini, S., Schuster-Böckler, B., & Graham, T. A. (2018) · Nature Communications · doi:10.1038/s41467-018-04208-6 · Cited by 115
Fu, C., Liang, X., Cui, W., Ober-Blöbaum, J. L., Vazzana, J., Shrikant, P. A., Lee, K. P., Clausen, B. E., Mellman, I., & Jiang, A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414167112 · Cited by 112
RNF43 and ZNRF3 are commonly altered in serrated pathway colorectal tumorigenesis
Bond, C., McKeone, D., Kalimutho, M., Bettington, M. L., Pearson, S., Dumenil, T. D., Wockner, L. F., Burge, M., Leggett, B., & Whitehall, V. (2016) · Oncotarget · doi:10.18632/oncotarget.12130 · Cited by 108
Synergy between Apc min and an Activated ras Mutation Is Sufficient To Induce Colon Carcinomas
D’Abaco, G. M., Whitehead, R. H., & Burgess, A. W. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.3.884 · Cited by 107
Tankyrase Inhibition Causes Reversible Intestinal Toxicity in Mice with a Therapeutic Index < 1
Zhong, Y., Katavolos, P., Nguyen, T., Lau, T., Boggs, J. W., Sambrone, A., Kan, D., Merchant, M. A., Harstad, E. B., Diaz, D., et al. (2015) · Toxicologic Pathology · doi:10.1177/0192623315621192 · Cited by 107
Frequent up-regulation of WNT2 in primary gastric cancer and colorectal cancer
Katoh, M. (2001) · International Journal of Oncology · doi:10.3892/ijo.19.5.1003 · Cited by 105
Insight into the Role of Wnt5a-Induced Signaling in Normal and Cancer Cells
Endo, M., Nishita, M., Fujii, M., & Minami, Y. (2014) · International review of cytology · doi:10.1016/bs.ircmb.2014.10.003 · Cited by 103
Bone loss from Wnt inhibition mitigated by concurrent alendronate therapy
Madan, B., McDonald, M. J., Foxa, G. E., Diegel, C. R., Williams, B. O., & Virshup, D. M. (2018) · Bone Research · doi:10.1038/s41413-018-0017-8 · Cited by 103
Synthetic Lethality of Wnt Pathway Activation and Asparaginase in Drug-Resistant Acute Leukemias
Hinze, L., Pfirrmann, M., Karim, S., Degar, J., McGuckin, C., Vinjamur, D. S., Sacher, J. R., Stevenson, K. E., Neuberg, D. S., Orellana, E. A., et al. (2019) · Cancer Cell · doi:10.1016/j.ccell.2019.03.004 · Cited by 103
Promotion of growth factor signaling as a critical function of β-catenin during HCC progression
Kim, E., Lisby, A., Ma, C. C., Lo, N., Ehmer, U., Hayer, K. E., Furth, E. E., & Viatour, P. (2019) · Nature Communications · doi:10.1038/s41467-019-09780-z · Cited by 102
Leedham, S. J., Rodenas-Cuadrado, P., Howarth, K. M., Lewis, A., Mallappa, S., Segditsas, S., Belnoue-Davis, H. L., Jeffery, R. E., Rodriguez‐Justo, M., Keshav, S., et al. (2012) · Gut · doi:10.1136/gutjnl-2011-301601 · Cited by 101
Büchert, M., Athineos, D., Abud, H. E., Burke, Z. D., Faux, M. C., Samuel, M. S., Jarnicki, A., Winbanks, C. E., Newton, I. P., Méniel, V. S., et al. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000816 · Cited by 98
Xu, X., Sun, P.-L., Li, J.-Z., Jheon, S., Lee, C.-T., & Chung, J.-H. (2011) · Journal of Thoracic Oncology · doi:10.1097/jto.0b013e31820c5189 · Cited by 97
Molecular regulation and pharmacological targeting of the β‐catenin destruction complex
van Kappel, E. C., & Maurice, M. M. (2017) · British Journal of Pharmacology · doi:10.1111/bph.13922 · Cited by 96
RAPGEF5 Regulates Nuclear Translocation of β-Catenin
Griffin, J. N., Viso, F. D., Duncan, A. R., Robson, A., Hwang, W. Y., Kulkarni, S. S., Liu, K. J., & Khokha, M. K. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.12.001 · Cited by 93
Marquardt, J. U., Seo, D., Andersen, J. B., Gillen, M. C., Kim, M. S., Conner, E. A., Galle, P. R., Factor, V. M., Park, Y. N., & Thorgeirsson, S. S. (2013) · Journal of Hepatology · doi:10.1016/j.jhep.2013.10.014 · Cited by 91
Canonical and non-canonical Wnt signaling are simultaneously activated by Wnts in colon cancer cells
Flores-Hernández, E., Velázquez, D. M., Castañeda‐Patlán, M. C., Fuentes-García, G., Fonseca‐Camarillo, G., Yamamoto-Furusho, J. K., Romero‐Ávila, M. T., García-Sáinz, J. A., & Robles‐Flores, M. (2020) · Cellular Signalling · doi:10.1016/j.cellsig.2020.109636 · Cited by 90
Distinct Colorectal Cancer–Associated APC Mutations Dictate Response to Tankyrase Inhibition
Schatoff, E. M., Goswami, S., Zafra, M. P., Foronda, M., Shusterman, M., Leach, B. I., Katti, A., Diaz, B. J., & Dow, L. E. (2019) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-0289 · Cited by 89
Self-citationMcGonigle, S., Chen, Z., Wu, J., Chang, P., Kolber, D. L., Ackermann, K. E., Twine, N. C., Shie, J., Miu, J. T., Huang, K., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5846 · Cited by 88
RSPO3 expands intestinal stem cell and niche compartments and drives tumorigenesis
Hilkens, J., Timmer, N. C., Boer, M., Ikink, G. J., Schewe, M., Sacchetti, A., Koppens, M. A. J., Song, J., & Bakker, E. R. M. (2016) · Gut · doi:10.1136/gutjnl-2016-311606 · Cited by 88
Interactions and functions of the adenomatous polyposis coli (APC) protein at a glance
Nelson, S., & Näthke, I. S. (2013) · Journal of Cell Science · doi:10.1242/jcs.100479 · Cited by 87
PORCN inhibition synergizes with PI3K/mTOR inhibition in Wnt-addicted cancers
Zhong, Z., Sepramaniam, S., Chew, X. H., Wood, K. C., Lee, M. A., Madan, B., & Virshup, D. M. (2019) · Oncogene · doi:10.1038/s41388-019-0908-1 · Cited by 86
Gaspar, C., Franken, P., Molenaar, L., Breukel, C., van der Valk, M., Smits, R., & Fodde, R. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000547 · Cited by 82
Lineage Reversion Drives WNT Independence in Intestinal Cancer
Han, T., Goswami, S., Hu, Y., Tang, F., Zafra, M. P., Murphy, C. J., Cao, Z., Poirier, J. T., Khurana, E., Elemento, O., et al. (2020) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-1536 · Cited by 81
Self-citationPeng, Y., He, Y., Chen, C., Xu, T., Li, L., Ni, M.-M., Meng, X., Huang, C., & Li, J. (2016) · Cancer Letters · doi:10.1016/j.canlet.2016.03.006 · Cited by 80
APC Mutations as a Potential Biomarker for Sensitivity to Tankyrase Inhibitors in Colorectal Cancer
Tanaka, N., Mashima, T., Mizutani, A., Sato, A., Aoyama, A., Gong, B., Yoshida, H., Muramatsu, Y., Nakata, K., Matsuura, M., et al. (2017) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-16-0578 · Cited by 80
Mizutani, A., Yashiroda, Y., Muramatsu, Y., Yoshida, H., Chikada, T., Tsumura, T., Okue, M., Shirai, F., Fukami, T., Yoshida, M., et al. (2018) · Cancer Science · doi:10.1111/cas.13805 · Cited by 79
Plummer, R., Dua, D., Cresti, N., Drew, Y., Stephens, P., Foegh, M. L., Knudsen, S., Sachdev, P., Mistry, B., Dixit, V. S., et al. (2020) · British Journal of Cancer · doi:10.1038/s41416-020-0916-5 · Cited by 74
Juan, J. M., Muraguchi, T., Iezza, G., Sears, R. C., & McMahon, M. (2014) · Genes & Development · doi:10.1101/gad.233627.113 · Cited by 73
Yamada, K., Hori, Y., Inoue, S., Yamamoto, Y., Iso, K., Kamiyama, H., Yamaguchi, A., Kimura, T., Uesugi, M., Ito, J., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-0782 · Cited by 71
Wnt pathway activation by ADP-ribosylation
Yang, E., Tacchelly‐Benites, O., Wang, Z., Randall, M. P., Tian, A., Benchabane, H., Freemantle, S. J., Pikielny, C. W., Tolwinski, N. S., Lee, E. N., et al. (2016) · Nature Communications · doi:10.1038/ncomms11430 · Cited by 69
Tu, J., Park, S.-H., Yu, W., Zhang, S., Wu, L., Carmon, K. S., & Liu, Q. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-54931-3 · Cited by 67
Picco, G., Petti, C., Centonze, A., Torchiaro, E., Crisafulli, G., Novara, L., Acquaviva, A., Bardelli, A., & Médico, E. (2017) · EMBO Molecular Medicine · doi:10.15252/emmm.201606773 · Cited by 62
Powell, A. E., Vlacich, G. R., Zhao, Z., McKinley, E. T., Washington, M. K., Manning, H. C., & Coffey, R. J. (2014) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00358.2013 · Cited by 62
Hinze, L., Labrosse, R., Degar, J., Han, T., Schatoff, E. M., Schreek, S., Karim, S., McGuckin, C., Sacher, J. R., Wagner, F. F., et al. (2020) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-1472 · Cited by 62
Self-citationA novel tankyrase inhibitor, MSC2504877, enhances the effects of clinical CDK4/6 inhibitors
Menon, M. R., Elliott, R. J. R., Bowers, L., Balan, N., Rafiq, R., Costa-Cabral, S., Munkonge, F. M., Trinidade, I., Porter, R. A., Campbell, A. D., et al. (2019) · Scientific Reports · doi:10.1038/s41598-018-36447-4 · Cited by 60
Leibold, J., Ruscetti, M. A., Cao, Z., Ho, Y.-J., Baslan, T., Zou, M., Abida, W. M., Feucht, J., Han, T., Barriga, F. M., et al. (2020) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-1242 · Cited by 56
Self-citationSolberg, N. T., Waaler, J., Lund, K., Mygland, L., Olsen, P. A., & Krauss, S. J. K. (2017) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-17-0362 · Cited by 53
The Functional Landscape of Patient-Derived RNF43 Mutations Predicts Sensitivity to Wnt Inhibition
Yu, J., Yusoff, P. A. M., Woutersen, D. T. J., Goh, P., Harmston, N., Smits, R., Epstein, D. M., Virshup, D. M., & Madan, B. (2020) · Cancer Research · doi:10.1158/0008-5472.can-20-0957 · Cited by 53
Li, B., Orton, D., Neitzel, L. R., Astudillo, L., Shen, C., Long, J., Chen, X., Kirkbride, K. C., Doundoulakis, T., Guerra, M. L., et al. (2017) · Science Signaling · doi:10.1126/scisignal.aak9916 · Cited by 51
TMEM59 potentiates Wnt signaling by promoting signalosome formation
Gerlach, J. P., Jordens, I., Tauriello, D. V. F., Kuper, I., Bugter, J. M., Noordstra, I., van der Kooij, J., Low, T. Y., Pimentel‐Muiños, F. X., Xanthakis, D., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1721321115 · Cited by 50
Li, S., Lavrijsen, M., Bakker, A., Magierowski, M., Magierowska, K., Liu, P., Wang, W., Peppelenbosch, M. P., & Smits, R. (2020) · Oncogene · doi:10.1038/s41388-020-1232-5 · Cited by 49
Schoumacher, M., Hurov, K. E., Lehár, J., Yan‐Neale, Y., Mishina, Y. M., Sonkin, D., Korn, J. M., Flemming, D., Jones, M. D., Antonakos, B., et al. (2014) · Cancer Research · doi:10.1158/0008-5472.can-14-0138-t · Cited by 46
β-Catenin inhibition shapes tumor immunity and synergizes with immunotherapy in colorectal cancer
Wang, C., Yan, J., Yin, P., Gui, L., Ji, L., Ma, B., & Gao, W. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1809947 · Cited by 46
RNF43 truncations trap CK1 to drive niche‐independent self‐renewal in cancer
Spit, M., Fenderico, N., Jordens, I., Radaszkiewicz, T. W., Lindeboom, R. G. H., Bugter, J. M., Cristobal, A., Ootes, L., van Osch, M., Janssen, E., et al. (2020) · The EMBO Journal · doi:10.15252/embj.2019103932 · Cited by 44
Integrative analysis of aberrant Wnt signaling in hepatitis B virus-related hepatocellular carcinoma
Ding, S. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i20.6317 · Cited by 41
Wnt pathway is involved in advanced gastric carcinoma.
Zhang, H., & Xue, Y. (2008) · PubMed · Cited by 40
ShRNA-mediated gene silencing of β-catenin inhibits growth of human colon cancer cells
Huang, W., Wang, J., Wang, T., Fang, J., Lan, P., & Ma, J.-P. (2007) · World Journal of Gastroenterology · doi:10.3748/wjg.v13.i48.6581 · Cited by 39
Yanai, H., Atsumi, N., Tanaka, T., Nakamura, N., Komai, Y., Omachi, T., Tanaka, K., Ishigaki, K., Saiga, K., Ohsugi, H., et al. (2017) · Scientific Reports · doi:10.1038/srep41838 · Cited by 39
Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor
Waaler, J., Leenders, R. G. G., Sowa, S. T., Brinch, S. A., Lycke, M., Nieczypor, P., Aertssen, S., Murthy, S., Galera‐Prat, A., Damen, E., et al. (2020) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c00208 · Cited by 39
Pai, P., Rachagani, S., Lakshmanan, I., Macha, M. A., Sheinin, Y. M., Smith, L. M., Ponnusamy, M. P., & Batra, S. K. (2015) · Molecular Oncology · doi:10.1016/j.molonc.2015.10.005 · Cited by 34
Wu, D., Jiang, Y., He, R., Tao, L., Yang, M., Fu, X., Yang, J.-Y., & Zhu, K. (2018) · Scientific Reports · doi:10.1038/s41598-018-34094-3 · Cited by 34
Moon, J.-H., Hong, S., Kim, J. E., Shin, J.-S., Kim, J.-S., Jung, S.-A., Ha, S. H., Lee, S., Kim, J., Lee, D. H., et al. (2019) · British Journal of Cancer · doi:10.1038/s41416-019-0434-5 · Cited by 34
Destruction complex dynamics: Wnt/β-catenin signaling alters Axin-GSK3β interactions inin vivo
Lybrand, D. B., Naiman, M., Laumann, J. M., Boardman, M., Petshow, S., Hansen, K., Scott, G. D., & Wehrli, M. (2019) · Development · doi:10.1242/dev.164145 · Cited by 34
Bmi1 is required for tumorigenesis in a mouse model of intestinal cancer
Maynard, M. A., Ferretti, R., Hilgendorf, K. I., Perret, C., Whyte, P., & Lees, J. A. (2013) · Oncogene · doi:10.1038/onc.2013.333 · Cited by 33
Real-time imaging of β-catenin dynamics in cells and living mice
Naik, S. U., & Piwnica-Worms, D. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704465104 · Cited by 33
Bo, H., Gao, L., Chen, Y., Zhang, J., & Zhu, M.-H. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4642 · Cited by 32
Wang, X., Wang, X., Liu, Y., Dong, Y., Wang, Y., Kassab, M. A., Fan, W., Yu, X., & Wu, C. (2018) · Oncogenesis · doi:10.1038/s41389-018-0071-5 · Cited by 32
Cai, J., Xiong, Q., Jiang, X.-L., Zhou, S., & Liu, T. (2018) · Experimental Cell Research · doi:10.1016/j.yexcr.2018.11.019 · Cited by 31
Jankú, F., Connolly, R. M., LoRusso, P. M., de Jonge, M., Vaishampayan, U. N., Rodon, J. A., Argilés, G., Myers, A. P., Schmitz, S. H., Ji, Y., et al. (2015) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.targ-15-c45 · Cited by 27
Schaefer, K. N., Pronobis, M. I., Williams, C. E., Zhang, S., Bauer, L., Goldfarb, D., Yan, F., Major, M. B., & Peifer, M. A. (2020) · Molecular Biology of the Cell · doi:10.1091/mbc.e19-11-0647 · Cited by 26
TMEM88 Inhibits Wnt Signaling by Promoting Wnt Signalosome Localization to Multivesicular Bodies
Lee, H., & Evans, T. (2019) · iScience · doi:10.1016/j.isci.2019.07.039 · Cited by 24
Borrelli, C., Valenta, T., Handler, K., Vélez, K., Gurtner, A., Moro, G., Lafzi, A., Roditi, L. D. V., Hausmann, G., Arnold, I. C., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21591-9 · Cited by 23
Yeung, P., Beviglia, L., Cancilla, B., Dee-Hoskins, C., Evans, J., Fischer, M. M., Yen, W.-C., Gurney, A. L., Lewicki, J. A., Hoey, T. C., et al. (2014) · Cancer Research · doi:10.1158/1538-7445.am2014-1907 · Cited by 20
van de Moosdijk, A. A. A., van de Grift, Y. B. C., de Man, S. M. A., Zeeman, A. L., & van Amerongen, R. (2020) · genesis · doi:10.1002/dvg.23387 · Cited by 18
Cui, L., Zhao, J., & Liu, J. (2017) · The American Journal of the Medical Sciences · doi:10.1016/j.amjms.2017.11.017 · Cited by 17
Tankyrase inhibition sensitizes cells to CDK4 blockade
Foronda, M., Tarumoto, Y., Schatoff, E. M., Leach, B. I., Diaz, B. J., Zimmerman, J., Goswami, S., Shusterman, M., Vakoc, C. R., & Dow, L. E. (2019) · PLoS ONE · doi:10.1371/journal.pone.0226645 · Cited by 17
Self-citationKim, S. J., García‐Recio, S., Creighton, C. J., Perou, C. M., & Rosen, J. M. (2019) · Oncogene · doi:10.1038/s41388-019-0852-0 · Cited by 16
Molecular landscape of colorectal cancers harboring R-spondin fusions.
Seeber, A., Kocher, F., Xiu, J., Spizzo, G., Puccini, A., Swensen, J. J., Ellis, M., Goldberg, R. M., Grothey, A. F., Shields, A. F., et al. (2019) · Journal of Clinical Oncology · doi:10.1200/jco.2019.37.15_suppl.3588 · Cited by 11
Woodcock, S. A., Bhamra, I., Jones, C., Cook, A. E., Eagle, C., & Phillips, C. (2019) · Cancer Research · doi:10.1158/1538-7445.am2019-3874 · Cited by 5
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Wnt/β-catenin signaling pathway in carcinogenesis and cancer therapy
Song, P., Gao, Z., Bao, Y., Chen, L., Huang, Y., Liu, Y., Dong, Q., & Wei, X. (2024) · Journal of Hematology & Oncology · doi:10.1186/s13045-024-01563-4 · Cited by 382
Lineage tracing reveals the phylodynamics, plasticity, and paths of tumor evolution
Yang, D., Jones, M. G., Naranjo, S., Rideout, W. M., Min, K. H., Ho, R., Wu, W., Replogle, J. M., Page, J. L., Quinn, J. J., et al. (2022) · Cell · doi:10.1016/j.cell.2022.04.015 · Cited by 349
Mechanisms of metastatic colorectal cancer
Cañellas-Socias, A., Sancho, E., & Batlle, E. (2024) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-024-00934-z · Cited by 284
WNT signaling and cancer stemness
Katoh, M., & Katoh, M. (2022) · Essays in Biochemistry · doi:10.1042/ebc20220016 · Cited by 188
Kim, R., An, M., Lee, H., Mehta, A., Heo, Y. J., Kim, K.-M., Lee, S.-Y., Moon, J., Kim, S. T., Min, B.-H., et al. (2021) · Cancer Discovery · doi:10.1158/2159-8290.cd-21-0888 · Cited by 181
Metadata
- Authors
- Parsons, M. J., Tammela, T., & Dow, L. E.
- Affiliations
- Weill Cornell Medicine (US)
- Memorial Sloan Kettering Cancer Center (US)
- Corresponding author
- Dow, Lukas E.
- Venue
- Cancer Discovery
- Published
- 2021-09-13
- Volume
- 11
- Issue
- 10
- Pages
- 2413-2429
- ISSN
- 2159-8274 (ISSN-L)
- 2159-8290
- PMC
- PMC8487948
- OpenAlex
- W3199697997
- Cited by
- 257
- References
- 195
- Citations by year
- 2026: 36 · 2025: 50 · 2024: 70 · 2023: 56 · 2022: 41 · 2021: 4
- FWCI
- 4.56
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Cancer Discovery (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- American Cancer Society (131461-RSG-17-202-01-TBG)
- NCI (1R01CA222517-01A1)
- Starr Cancer Consortium (SCC I14-0023)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Hedgehog Signaling Pathway Studies
- Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
- Keywords
- Wnt signaling, carcinogenesis, tumor immune microenvironment, immune evasion, Wnt pathway inhibitors, cancer therapy, tissue homeostasis
- MeSH terms
- Humans, Neoplasms, Tumor Microenvironment, Wnt Signaling Pathway, 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.
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