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Wnt signaling and cancer
Open accessAbstract
The regulation of cell growth and survival can be subverted by a variety of genetic defects that alter transcriptional programs normally responsible for controlling cell number. High throughput analysis of these gene expression patterns should ultimately lead to the identification of minimal expression profiles that will serve as common denominators in assigning a cancer to a given category. In the course of defining the common denominators, though, we should not be too surprised to find that cancers within a single category may nevertheless exhibit seemingly disparate genetic defects. The wnt pathway has already provided an outstanding example of this. We now know of three regulatory genes in this pathway that are mutated in primary human cancers and several others that promote experimental cancers in rodents (Fig. 1). In all of these cases the common denominator is the activation of gene transcription by -catenin. The resulting gene expression profile should provide us with a signature common to those cancers carrying defects in the wnt pathway. In this review, the wnt pathway will be covered from the perspective of cancer, with emphasis placed on molecular defects known to promote neoplastic transformation in humans and in animal models.
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“Constitutive activation of this pathway is also implicated in cancer development in several other organs (140).”
From Adrenal incidentaloma (2020) · cites this paper as [140]
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Citations
Cites
Identification of c- MYC as a Target of the APC Pathway
He, T.-C., Sparks, A. B., Rago, C., Hermeking, H., Zawel, L., da Costa, L. T., Morin, P. J., Vogelstein, B., & Kinzler, K. W. (1998) · Science · doi:10.1126/science.281.5382.1509 · Cited by 4,566
Activation of β-Catenin-Tcf Signaling in Colon Cancer by Mutations in β-Catenin or APC
Morin, P. J., Sparks, A. B., Kořínek, V., Barker, N., Clevers, H. C., Vogelstein, B., & Kinzler, K. W. (1997) · Science · doi:10.1126/science.275.5307.1787 · Cited by 4,000
β-Catenin regulates expression of cyclin D1 in colon carcinoma cells
Tetsu, O., & McCormick, F. (1999) · Nature · doi:10.1038/18884 · Cited by 3,601
Functional interaction of β-catenin with the transcription factor LEF-1
Behrens, J., von Kries, J. P., Kühl, M., Bruhn, L., Wedlich, D., Grosschedl, R., & Birchmeier, W. (1996) · Nature · doi:10.1038/382638a0 · Cited by 2,912
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
Identification of FAP Locus Genes from Chromosome 5q21
Kinzler, K. W., Nilbert, M. C., Su, L.-K., Vogelstein, B., Bryan, T. M., Levy, D. B., Smith, K. J., Preisinger, A. C., Hedge, P., McKechnie, D., et al. (1991) · Science · doi:10.1126/science.1651562 · Cited by 2,331
The cyclin D1 gene is a target of the β-catenin/LEF-1 pathway
Shtutman, M., Zhurinsky, J., Simcha, I., Albanese, C., D’Amico, M., Pestell, R., & Ben-Ze’ev, A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.10.5522 · Cited by 2,230
MECHANISMS OF WNT SIGNALING IN DEVELOPMENT
Wodarz, A., & Nusse, R. (1998) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.14.1.59 · Cited by 2,030
Nusse, R., & VARMUS, H. E. (1982) · Cell · doi:10.1016/0092-8674(82)90409-3 · Cited by 1,864
XTcf-3 Transcription Factor Mediates β-Catenin-Induced Axis Formation in Xenopus Embryos
Molenaar, M., van de Wetering, M., Oosterwegel, M., Peterson-Maduro, J., Godsave, S., Korinek, V., Roose, J., Destrée, O., & Clevers, H. (1996) · Cell · doi:10.1016/s0092-8674(00)80112-9 · Cited by 1,824
Research works printed but not linked: 1
- 10.1210/jc.85.1.286 · DOI
Cited by
Sorted by citations
Items 301–400 of 1,005
Zhao, W., Ji, X., Zhang, F., Li, L., & Ma, L. (2012) · Molecules · doi:10.3390/molecules17066196 · Cited by 235
“Fzd has a large extracellular N-terminal region containing a cysteine-rich domain (CRD), which is involved in the binding to Wnt proteins [36,40].”
BackgroundCasein kinase I phosphorylates and destabilizes the β-catenin degradation complex
Gao, Z.-H., Seeling, J. M., Hill, V., Yochum, A., & Virshup, D. M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.032468199 · Cited by 225
Exon 3 mutations of CTNNB1 drive tumorigenesis: a review
Gao, C., Wang, Y., Broaddus, R. R., Sun, L., Xue, F., & Zhang, W. (2017) · Oncotarget · doi:10.18632/oncotarget.23695 · Cited by 227
“Paul Polakis (2000) has summarized CTNNB1 mutation spots and rates in human cancers in detail [93].”
BackgroundCrystal Structure of a β-Catenin/BCL9/Tcf4 Complex
Sampietro, J., Dahlberg, C. L., Cho, U., Hinds, T. R., Kimelman, D., & Xu, W. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.09.001 · Cited by 225
Glycosylation and palmitoylation of Wnt‐3a are coupled to produce an active form of Wnt‐3a
Komekado, H., Yamamoto, H., Chiba, T., & Kikuchi, A. (2007) · Genes to Cells · doi:10.1111/j.1365-2443.2007.01068.x · Cited by 231
Wnt/beta-Catenin Signaling and Small Molecule Inhibitors
Voronkov, A. E., & Krauss, S. J. K. (2012) · Current Pharmaceutical Design · doi:10.2174/138161213804581837 · Cited by 227
Li, N., Kaur, P., Bunnag, N., Suresh, J., Sung, I. C. H., Tan, Q. H., Gruber, J., & Tolwinski, N. S. (2019) · Cells · doi:10.3390/cells8080826 · Cited by 228
“Inappropriate activation of the WNT pathway is also a major factor in human oncogenesis [4].”
BackgroundThe anticancer activity of propolis
Sawicka, D., Car, H., Borawska, M. H., & Nikliński, J. (2012) · Folia Histochemica et Cytobiologica · doi:10.5603/fhc.2012.0004 · Cited by 227
Beta-catenin signaling, liver regeneration and hepatocellular cancer: sorting the good from the bad
Nejak-Bowen, K. N., & Monga, S. P. S. (2011) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2010.12.010 · Cited by 260
Acetylation of β-Catenin by p300 Regulates β-Catenin-Tcf4 Interaction
Lévy, L., Yu, W., Labalette, C., Wu, Y., Renard, C.-A., Buendia, M. A., & Neuveut, C. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.8.3404-3414.2004 · Cited by 220
Cha, M.-Y., Kim, C.-M., Park, Y.-M., & Ryu, W. (2004) · Hepatology · doi:10.1002/hep.20245 · Cited by 223
Moon, R. T. (2005) · Science s STKE · doi:10.1126/stke.2712005cm1 · Cited by 225
Metabolic Reprogramming of Colorectal Cancer Cells and the Microenvironment: Implication for Therapy
Nenkov, M., Ma, Y., Gaßler, N., & Chen, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126262 · Cited by 226
Jung, A., Schrauder, M., Oswald, U., Knoll, C., Sellberg, P., Palmqvist, R., Niedobitek, G., Brabletz, T., & Kirchner, T. (2001) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63007-6 · Cited by 217
Targeting the β-catenin/TCF transcriptional complex in the treatment of multiple myeloma
Sukhdeo, K., Mani, M., Zhang, Y., Dutta, J., Yasui, H., Rooney, M., Carrasco, D. E., Zheng, M., He, H., Tai, Y., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610299104 · Cited by 219
Kemp, C. R., Willems, E., Abdo, S., Lambiv, L., & Leyns, L. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20408 · Cited by 219
Epidermal Growth Factor Receptor: A Novel Target of the Wnt/β-Catenin Pathway in Liver
Tan, X., Apte, U. M., Micsenyi, A., Kotsagrelos, E., Luo, J.-H., Ranganathan, S., Monga, D. K., Bell, A. W., Michalopoulos, G. K., & Monga, S. P. (2005) · Gastroenterology · doi:10.1053/j.gastro.2005.04.013 · Cited by 219
Ju, J., Hong, J., Zhou, J.-N., Pan, Z., Bose, M., Liao, J., Yang, G., Liu, Y. Y., Hou, Z., Lin, Y., et al. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-1949 · Cited by 222
RUNX3 Attenuates β-Catenin/T Cell Factors in Intestinal Tumorigenesis
Ito, K., Lim, A. C. B., Salto‐Tellez, M., Motoda, L., Osato, M., Chuang, L. S. H., Lee, C. W. L., Voon, D. C., Koo, J. K. W., Wang, H., et al. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.08.004 · Cited by 221
Conceptual Evolution of Cell Signaling
Nair, A., Chauhan, P. S., Saha, B., & Kubatzky, K. F. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20133292 · Cited by 238
“Not only the growth factor receptor pathway, but also defects in the Wnt signaling pathway, mainly β-catenin, represent an appropriate drug target in Wnt-signaling associated cancers [189].”
BackgroundProspective discovery of small molecule enhancers of an E3 ligase-substrate interaction
Simonetta, K. R., Taygerly, J., Boyle, K., Basham, S. E., Padovani, C., Lou, Y., Cummins, T. J., Yung, S. L., von Soly, S. K., Kayser, F., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09358-9 · Cited by 217
The c‐myc Promoter: Still MysterY and Challenge
(2008) · Advances in Cancer Research · doi:10.1016/s0065-230x(07)99004-1 · Cited by 211
Tcf4 can specifically recognize beta-catenin using alternative conformations.
Graham, T. A., Ferkey, D. M., Mao, F., Kimelman, D., & Xu, W. (2001) · Nature Structural Biology · doi:10.1038/nsb718 · Cited by 219
The GSK-3 Inhibitor BIO Promotes Proliferation in Mammalian Cardiomyocytes
Tseng, A.-S. K., Engel, F. B., & Keating, M. T. (2006) · Chemistry & Biology · doi:10.1016/j.chembiol.2006.08.004 · Cited by 218
Wu, G., Huang, H., Abreu, J. G., & He, X. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004926 · Cited by 216
The way Wnt works: Components and mechanism
Saito‐Diaz, K., Chen, T. W., Wang, X., Thorne, C. A., Wallace, H. A., Page, A. W., & Lee, E. N. (2012) · Growth Factors · doi:10.3109/08977194.2012.752737 · Cited by 223
“In addition, to these point mutations, N-terminal in-frame deletions of b-catenin (which remove the GSK3 and CK1a phosphorylation sites) have also been described in cancers (Peifer and Polakis 2000; Laurent-Puig et al. 2001).”
BackgroundInfluentialXu, J., Zhu, X., Wu, L., Yang, R., Yang, Z., Wang, Q., & Wu, F. (2012) · Liver International · doi:10.1111/j.1478-3231.2011.02750.x · Cited by 215
Prostaglandin E2 Stimulates the β-Catenin/T Cell Factor-dependent Transcription in Colon Cancer
Shao, J., Jung, C., Liu, C., & Sheng, H. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413056200 · Cited by 216
Impact of cytomorphological detection of circulating tumor cells in patients with liver cancer
Vona, G., Estepa, L., Béroud, C., Damotte, D., Capron, F., Nalpas, B., Mineur, A., Franco, D., Lacour, B., Pol, S., et al. (2004) · Hepatology · doi:10.1002/hep.20091 · Cited by 215
Tarte, K., Zhan, F., Vos, J. D., Klein, B., & Shaughnessy, J. D. (2003) · Blood · doi:10.1182/blood-2002-10-3161 · Cited by 215
Stein, U., Arlt, F., Walther, W., Smith, J. L., Waldman, T. A., Harris, E. D., Mertins, S. D., Heizmann, C. W., Allard, D., Birchmeier, W., et al. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.08.041 · Cited by 214
Maintenance of hematopoietic stem cells through regulation of Wnt and mTOR pathways
Huang, J. Y., Nguyen-McCarty, M., Hexner, E. O., Danet-Desnoyers, G. A., & Klein, P. S. (2012) · Nature Medicine · doi:10.1038/nm.2984 · Cited by 221
Crystal Structure of a Full-Length β-Catenin
Xing, Y., Takemaru, K., Liu, J., Berndt, J. D., Zheng, J., Moon, R. T., & Xu, W. (2008) · Structure · doi:10.1016/j.str.2007.12.021 · Cited by 233
Mesenchymal Stem Cell-Mediated Effects of Tumor Support or Suppression
Rhee, K., Lee, J. E., & Eom, Y. W. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161226215 · Cited by 221
“The WNT signaling pathway has also been associated with the development of carcinomas of the breast, liver, colon, skin, stomach, and ovary [160–171].”
BackgroundMurdoch, B., Chadwick, K., Martin, M. A., Shojaei, F., Shah, K. V., Gallacher, L. M., Moon, R. T., & Bhatia, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0130233100 · Cited by 214
Impact of p53 loss on reversal and recurrence of conditional Wnt-induced tumorigenesisPreprint
Gunther, E. J., Moody, S. E., Belka, G. K., Hahn, K. T., Innocent, N., Dugan, K. D., Cardiff, R. D., & Chodosh, L. A. (2003) · Genes & Development · doi:10.1101/gad.1051603 · Cited by 214
Identification of a Specific Inhibitor of the Dishevelled PDZ Domain
Shan, J., Shi, D., Wang, J., & Zheng, J. (2005) · Biochemistry · doi:10.1021/bi0512602 · Cited by 211
Sureban, S. M., May, R. J., Lightfoot, S. A., Hoskins, A. B., Lerner, M. R., Brackett, D. J., Postier, R. G., Ramanujam, R. P., Mohammed, A., Rao, C. V., et al. (2011) · Cancer Research · doi:10.1158/0008-5472.can-10-2738 · Cited by 213
Regulation of Wnt signaling by protein-protein interaction and post-translational modifications
Kikuchi, A., Kishida, S., & Yamamoto, H. (2006) · Experimental & Molecular Medicine · doi:10.1038/emm.2006.1 · Cited by 217
Yang, J., Zhang, W., Evans, P. M., Chen, X., He, X., & Liu, C. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600831200 · Cited by 219
Cadherin Signaling in Cancer: Its Functions and Role as a Therapeutic Target
Yu, W., Yang, L., Li, T., & Zhang, Y. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.00989 · Cited by 214
“keep the low level of β-catenin in cytoplasm, as well as cell nucleus (56).”
BackgroundLee, S., Cekanova, M., & Baek, S. J. (2007) · Molecular Carcinogenesis · doi:10.1002/mc.20374 · Cited by 212
Wnt signaling promotes oncogenic transformation by inhibiting c-Myc–induced apoptosis
You, Z., Saims, D., Chen, S., Zhang, Z., Guttridge, D. C., Guan, K., MacDougald, O. A., Brown, A. M. C., Evan, G. I., Kitajewski, J., et al. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200201110 · Cited by 211
Sarrió, D., Moreno‐Bueno, G., Hardisson, D., Sánchez‐Estévez, C., Guo, M., Herman, J. G., Gamallo, C., Esteller, M., & Palacios, J. (2003) · International Journal of Cancer · doi:10.1002/ijc.11197 · Cited by 211
Green, R. A., & Kaplan, K. B. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200307070 · Cited by 211
Wrch-1, a novel member of the Rho gene family that is regulated by Wnt-1Preprint
Tao, W., Pennica, D., Xu, L., Kalejta, R. F., & Levine, A. J. (2001) · Genes & Development · doi:10.1101/gad.894301 · Cited by 210
Townsley, F. M., Cliffe, A., & Bienz, M. (2004) · Nature Cell Biology · doi:10.1038/ncb1141 · Cited by 209
Wnt Signaling Pathway in Mammary Gland Development and Carcinogenesis
Turashvili, G., Bouchal, J., Burkadze, G., & Kolář, Z. (2006) · Pathobiology · doi:10.1159/000098207 · Cited by 210
The WNT signalling pathway and diabetes mellitus
Jin, T. (2008) · Diabetologia · doi:10.1007/s00125-008-1084-y · Cited by 211
Jiang, Z., Jiang, X., Chen, S., Lai, Y., Wei, X., Li, B., Lin, S., Wang, S., Wu, Q., Liang, Q., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00690 · Cited by 207
“Previous studies show that MET and CTNNB1 act as oncogenes in HCCs and that CCND1 is the hallmark of cell cycle progression (19, 26, 27).”
BackgroundDamalas, A., Kahan, S., Shtutman, M. S., Ben‐Ze'ev, A., & Oren, M. (2001) · The EMBO Journal · doi:10.1093/emboj/20.17.4912 · Cited by 208
New Insights into the Mechanism of Action of Soluble Klotho
Dalton, G. D., Xie, J., An, S.-W., & Huang, C. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00323 · Cited by 210
“Wnt signaling is initiated when secreted Wnt ligands activate transmembrane receptors that promote the translocation of β-catenin to the nucleus where it induces the activity of transcription factors such as TCF and LEF (77).”
BackgroundGuo, X., Jiang, H., Shi, B., Zhou, M., Zhang, H., Shi, Z., Du, G., Luo, H., Wu, X., Wang, Y., et al. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01118 · Cited by 208
“Among three analyzed tumor-related genes, CTNNB1 and MET act as the oncogenes in HCC, and CCND1 is the hallmarker of cell cycle procession (Polakis, 2000; Zhang et al., 2002; Venepalli and Goff, 2013).”
BackgroundHayward, P., Brennan, K. R., Sanders, P., Balayo, T., DasGupta, R., Perrimon, N., & Arias, A. M. (2005) · Development · doi:10.1242/dev.01724 · Cited by 204
Zhang, C., Qi, L., Hunter, D. J., Meigs, J. B., Manson, J. E., van Dam, R. M., & Hu, F. B. (2006) · Diabetes · doi:10.2337/db06-0643 · Cited by 207
Kim, J., Zhang, X., Rieger‐Christ, K., Summerhayes, I. C., Wazer, D. E., Paulson, K. E., & Yee, A. S. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m513378200 · Cited by 204
Casein kinase I phosphorylates the Armadillo protein and induces its degradation in Drosophila
Yanagawa, S.-I., Matsuda, Y., Lee, J.-S., Matsubayashi, H., Sese, S., Kadowaki, T., & Ishimoto, A. (2002) · The EMBO Journal · doi:10.1093/emboj/21.7.1733 · Cited by 202
TCF: Lady Justice Casting the Final Verdict on the Outcome of Wnt Signalling
Brantjes, H., Barker, N., van Es, J. H., & Clevers, H. C. (2002) · Biological Chemistry · doi:10.1515/bc.2002.027 · Cited by 202
Bax, B. D., Carter, P. S., Lewis, C. J., Guy, A. R., Bridges, A. M., Tanner, R., Pettman, G. R., Mannix, C. J., Culbert, A. A., Brown, M. J. B., et al. (2001) · Structure · doi:10.1016/s0969-2126(01)00679-7 · Cited by 209
In vivo P2X7 inhibition reduces amyloid plaques in Alzheimer's disease through GSK3β and secretases
Díaz‐Hernandéz, J. I., Gómez‐Villafuertes, R., León‐Otegui, M., Hontecillas‐Prieto, L., del Puerto, A., Trejo, J. L., Lucas, J. J., Garrido, J. J., Gualix, J., Miras‐Portugal, M. T., et al. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.09.040 · Cited by 203
Epigenetic alterations involved in cancer stem cell reprogramming
Muñoz, P., Iliou, M. S., & Esteller, M. (2012) · Molecular Oncology · doi:10.1016/j.molonc.2012.10.006 · Cited by 205
“Gain-of-function mutations of the CTNNB1 gene (encoding b-catenin) and loss-offunction mutations of APC and AXIN genes were identified as the main mechanisms associated to Wnt signaling dysfunction in cancers (Barker and Clevers, 2006; Lindvall et al., 2007; Polakis, 2000).”
BackgroundWnt/?-catenin-pathway as a molecular target for future anti-cancer therapeutics
Dihlmann, S., & Doeberitz, M. V. K. (2004) · International Journal of Cancer · doi:10.1002/ijc.20609 · Cited by 204
Cadherins and the tumour progression: is it all in a switch?
Cavallaro, U., Schaffhauser, B., & Christofori, G. (2002) · Cancer Letters · doi:10.1016/s0304-3835(01)00759-5 · Cited by 201
Grotewold, L., & Rüther, U. (2002) · The EMBO Journal · doi:10.1093/emboj/21.5.966 · Cited by 201
Potential Targets for Prevention of Colorectal Cancer: a Focus on PI3K/Akt/mTOR and Wnt Pathways
Pandurangan, A. K. (2013) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2013.14.4.2201 · Cited by 198
“A deregulation in the Wnt signaling pathway disrupts axis formation in embryos (Heasman et al., 1994; Funayama et al., 1995; Laurent et al., 1997) and is associated with multiple human malignancies (Polakis, 2000).”
BackgroundEffects of Intestinal Microbial–Elaborated Butyrate on Oncogenic Signaling Pathways
Chen, J., Zhao, K., & Vitetta, L. (2019) · Nutrients · doi:10.3390/nu11051026 · Cited by 211
Exploration of liver cancer genomes
Shibata, T., & Aburatani, H. (2014) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2014.6 · Cited by 202
Both ERK and Wnt/β-catenin pathways are involved in Wnt3a-induced proliferation
Yun, M.-S., Kim, S., Jeon, S. H., Lee, J., & Choi, K. (2004) · Journal of Cell Science · doi:10.1242/jcs.01601 · Cited by 197
Colnot, S., Niwa‐Kawakita, M., Hamard, G., Godard, C., Plénier, S. L., Houbron, C., Romagnolo, B., Berrebi, D. D., Giovannini, M., & Perret, C. (2004) · Laboratory Investigation · doi:10.1038/labinvest.3700180 · Cited by 219
The Wnt connection to tumorigenesis
Behrens, J., & Lustig, B. (2004) · The International Journal of Developmental Biology · doi:10.1387/ijdb.041815jb · Cited by 200
Fattet, S., Haberler, C., Legoix, P., Varlet, P., Lellouch‐Tubiana, A., Lair, S., Manié, É., Raquin, M., Bours, D., Carpentier, S., et al. (2009) · The Journal of Pathology · doi:10.1002/path.2514 · Cited by 194
Role of APC and DNA mismatch repair genes in the development of colorectal cancers.
Narayan, S., & Roy, D. (2003) · Molecular Cancer · doi:10.1186/1476-4598-2-41 · Cited by 194
TCF Transcription Factors, Mediators of Wnt-Signaling in Development and Cancer
van Noort, M., & Clevers, H. C. (2002) · Developmental Biology · doi:10.1006/dbio.2001.0566 · Cited by 194
Axin is a scaffold protein in TGF‐β signaling that promotes degradation of Smad7 by Arkadia
Liu, W., Rui, H., Wang, J., Lin, S., He, Y., Chen, M., Li, Q., Ye, Z., Chan, S. C., Chan, S. C., et al. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601057 · Cited by 199
Inagawa, S., Itabashi, M., Adachi, S., Kawamoto, T., Hori, M., Shimazaki, J., Yoshimi, F., & Fukao, K. (2002) · PubMed · Cited by 193
The Canonical Wnt/β-Catenin Signalling Pathway
Barker, N. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-249-6_1 · Cited by 192
The KIF3 motor transports N-cadherin and organizes the developing neuroepithelium
Teng, J., Rai, T., Tanaka, Y., Takei, Y., Nakata, T., Hirasawa, M., Kulkarni, A. B., & Hirokawa, N. (2005) · Nature Cell Biology · doi:10.1038/ncb1249 · Cited by 195
Uematsu, K., Kanazawa, S., You, L., He, B., Xu, Z., Li, K., Peterlin, B. M., McCormick, F. P., & Jablons, D. M. (2003) · PubMed · Cited by 188
Guo, Z. S., Thorne, S. H., & Bartlett, D. L. (2008) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2008.02.001 · Cited by 198
Pollheimer, J., Loregger, T., Sonderegger, S., Saleh, L., Bauer, S., Bilban, M., Czerwenka, K. F., Husslein, P. W., & Knöfler, M. (2006) · American Journal Of Pathology · doi:10.2353/ajpath.2006.050686 · Cited by 191
Bikkavilli, R. K., Feigin, M. E., & Malbon, C. C. (2008) · Journal of Cell Science · doi:10.1242/jcs.032854 · Cited by 193
Flahaut, M., Meier, R., Coulon, A., Nardou, K., Niggli, F. K., Martinet, D., Beckmann, J. S., Joseph, J.-M., Mühlethaler‐Mottet, A., & Gross, N. (2009) · Oncogene · doi:10.1038/onc.2009.80 · Cited by 193
Nuclear-cytoplasmic shuttling of Axin regulates subcellular localization of β-catenin
Cong, F., & VARMUS, H. E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307344101 · Cited by 189
Involvement of RNA Helicases p68 and p72 in Colon Cancer
Shin, S., Rossow, K. L., Grande, J. P., & Janknecht, R. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-4652 · Cited by 190
Urakami, S., Shiina, H., Enokida, H., Kawakami, T., Tokizane, T., Ogishima, T., Tanaka, Y., Li, L.-C., Ribeiro‐Filho, L. A., Terashima, M., et al. (2006) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-05-1344 · Cited by 189
Wnt and Bmp signalling cooperatively regulate gradedEmx2 expression in the dorsal telencephalon
Theil, T., Aydin, S., Koch, S., Grotewold, L., & Rüther, U. (2002) · Development · doi:10.1242/dev.129.13.3045 · Cited by 189
Schwarz-Romond, T., Asbrand, C., Bakkers, J., Kühl, M., Schaeffer, H.-J., Huelsken, J., Behrens, J., Hammerschmidt, M., & Birchmeier, W. (2002) · Genes & Development · doi:10.1101/gad.230402 · Cited by 192
VEGF inhibition: insights from preclinical and clinical studies
Crawford, Y., & Ferrara, N. (2008) · Cell and Tissue Research · doi:10.1007/s00441-008-0675-8 · Cited by 192
Arendt, T. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.09.007 · Cited by 189
Mani, M., Carrasco, D. E., Zhang, Y., Takada, K., Gatt, M. E., Dutta-Simmons, J., Ikeda, H., Diaz‐Griffero, F., Peña‐Cruz, V., Bertagnolli, M. M., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-0773 · Cited by 191
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Boettner, B., & Van Aelst, L. (2002) · Gene · doi:10.1016/s0378-1119(02)00426-2 · Cited by 229
Cell–cell connectivity: desmosomes and disease
Brooke, M. A., Nitoiu, D., & Kelsell, D. P. (2011) · The Journal of Pathology · doi:10.1002/path.3027 · Cited by 190
Osafune, K., Takasato, M., Kispert, A., Asashima, M., & Nishinakamura, R. (2005) · Development · doi:10.1242/dev.02174 · Cited by 189
ΔNp63 induces β-catenin nuclear accumulation and signaling
Patturajan, M., Nomoto, S., Sommer, M., Fomenkov, A. I., Hibi, K., Zangen, R., Poliak, N., Califano, J. A., Trink, B., Ratovitski, E. A., et al. (2002) · Cancer Cell · doi:10.1016/s1535-6108(02)00057-0 · Cited by 187
Conacci‐Sorrell, M., Ben-Yedidia, T., Shtutman, M. S., Feinstein, E., Einat, P., & Ben‐Ze'ev, A. (2002) · Genes & Development · doi:10.1101/gad.227502 · Cited by 187
Glycogen synthase kinase-3β positively regulates the proliferation of human ovarian cancer cells
Cao, Q., Lu, X., & Feng, Y. (2006) · Cell Research · doi:10.1038/sj.cr.7310078 · Cited by 186
Ysebaert, L., Chicanne, G., Demur, C., de Toni, F., Prade, N., Ruidavets, J.-B., Mas, V. M., Huguet, F., Laurent, G., Payrastre, B., et al. (2006) · Leukemia · doi:10.1038/sj.leu.2404239 · Cited by 192
Role of serine/threonine protein phosphatase 2A in cancer
Schönthal, A. H. (2001) · Cancer Letters · doi:10.1016/s0304-3835(01)00561-4 · Cited by 186
Acetylation of β-Catenin by CREB-binding Protein (CBP)
Wolf, D., Rodova, M., Miska, E. A., Calvet, J. P., & Kouzarides, T. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201196200 · Cited by 194
Yang, M., Zhong, W., Srivastava, N., Slavin, A., Yang, J., Hoey, T., & An, S. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501535102 · Cited by 188
Metadata
- Authors
- Polakis, P.
- Affiliations
- Genentech (US)
- Corresponding author
- Polakis, Paul
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2000-08-01
- Volume
- 14
- Issue
- 15
- Pages
- 1837-1851
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- OpenAlex
- W2239090104
- Cited by
- 3,183
- References
- 190
- Citations by year
- 2026: 6 · 2025: 12 · 2024: 25 · 2023: 43 · 2022: 39 · 2021: 46 · 2020: 56 · 2019: 67 · 2018: 71 · 2017: 86 · 2016: 110 · 2015: 144 · 2014: 138 · 2013: 147 · 2012: 174
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed (publishedVersion)
- 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 › Signaling Pathways in Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Hedgehog Signaling Pathway Studies
- Keywords
- Wnt signaling, β-catenin, cancer, oncogenic transformation, transcriptional activation, gene expression profiles, experimental tumor model
- MeSH terms
- Dishevelled Proteins, Animals, Cytoskeletal Proteins, Humans, Neoplasms, Phosphoprotein Phosphatases, Phosphoproteins, Proto-Oncogene Proteins, Transcription Factors, Signal Transduction, Trans-Activators, Calcium-Calmodulin-Dependent Protein Kinases, Adenomatous Polyposis Coli Protein, Zebrafish Proteins, Glycogen Synthase Kinase 3, Adaptor Proteins, Signal Transducing, Wnt Proteins, beta Catenin
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