β-Catenin regulates expression of cyclin D1 in colon carcinoma cells (original) (raw)
Kinzler, K. & Vogelstein, B. Lessons from hereditary colorectal cancer. Cell87, 159–170 (1996). ArticleCAS Google Scholar
Munemitsu, S., Albert, I., Souza, B., Rubinfeld, B. & Polakis, P. Regulation of intracellular β-catenin levels by the adenomatous polyposis coli (APC) tumor-suppressor protein. Proc. Natl Acad. Sci. USA92, 3046–3050 (1995). ArticleADSCAS Google Scholar
Korinek, V. et al. Constitutive transcriptional activation by a β-catenin-Tcf complex in APC−/− colon carcinoma. Science275, 1784–1787 (1997). ArticleCAS Google Scholar
Morin, P. et al. Activation of β-catenin-Tcf signaling in colon cancer by mutations in β-catenin or APC. Science275, 1787–1790 (1997). ArticleCAS Google Scholar
Rubinfeld, B. et al. Stabilization of β-catenin by genetic defects in melanoma cell lines. Science275, 1790–1792 (1997). ArticleCAS Google Scholar
Zurawel, R., Chiappa, S., Allen, C. & Raffel, C. Sporadic medulloblastomas contain β-catenin mutations. Cancer Res.58, 896–899 (1998). CASPubMed Google Scholar
Voeller, H., Truica, C. & Gelmann, E. β-catenin mutations in human prostate cancer. Cancer Res.58, 2520–2523 (1998). CASPubMed Google Scholar
Kawanishi, J. et al. Loss of E-cadherin-dependent cell-cell adhesion due to a mutation of the β-catenin gene in a human cancer cell line, HSC-39. Mol. Cell. Biol.15, 1175–1181 (1995). ArticleCAS Google Scholar
Miyoshi, Y. et al. Activation of the β-catenin gene in primary hepatocellular carcinomas by somatic alterations involving Exon 3. Cancer Res.58, 2524–2527 (1998). CASPubMed Google Scholar
De La Coste, A. et al. Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas. Proc. Natl Acad. Sci. USA95, 8847–8851 (1998). ArticleADSCAS Google Scholar
Molenaar, M. et al. XTcf-3 transcription factor mediates β-catenin-induced axis formation in Xenopus embryos. Cell86, 391–399 (1996). ArticleCAS Google Scholar
Behrens, J. et al. Functional interaction of β-catenin with the transcription factor LEF-1. Nature382, 638–642 (1996). ArticleADSCAS Google Scholar
Clevers, H. & Grosschedl, R. Transcriptional control of lymphoid development: lessons from gene targeting. Immunol. Today17, 336–343 (1996). ArticleCAS Google Scholar
van de Wetering, M. et al. Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF. Cell88, 789–799 (1997). ArticleCAS Google Scholar
Geise, K., Kingsley, C., Kirshner, J. & Grosschedl, R. Assembly and function of a TCR-alpha enhancer complex is dependent on LEF-1-induced DNA bending and multiple protein-protein interactions. Genes Dev.9, 995–1008 (1995). Article Google Scholar
Huber, O. et al. Nuclear localization of β-catenin by interaction with transcription factor LEF-1. Mech. Dev.59, 310 (1996). Article Google Scholar
van der Heyden, M. et al. Identification of connexin43 as a target for wnt signaling. J. Cell Sci.111, 1741–1749 (1998). CASPubMed Google Scholar
Riese, J. et al. LEF-1, a nuclear factor coordinating signaling inputs from wingless and decapentaplegic. Cell88, 777–787 (1997). ArticleCAS Google Scholar
Brannon, M., Gomperts, M., Sumoy, L., Moon, R. & Kimelman, D. Aβ-catenin/XTcf-3 complex binds to the siamois promoter to regulate dorsal axis specification in Xenopus. Genes Dev.11, 2359–2370 (1997). ArticleCAS Google Scholar
McKendry, R., Hsu, S., Harland, R. & Grosschedl, R. LEF-1/TCF proteins mediate Wnt-inducible transcription from the Xenopus Nodal related 3 promoter. Dev. Biol.192, 420–431 (1997). ArticleCAS Google Scholar
He, T. et al. Identification of c-myc as a target of the APC pathway. Science281, 1509–1512 (1998). ArticleADSCAS Google Scholar
Arber, N. et al. Increased expression of cyclin D1 is an early event in multistage colorectal carcinogenesis. Gastroenterology110, 669–674 (1996). ArticleCAS Google Scholar
Arber, N. et al. Antisense to cyclin D1 inhibits the growth and tumorigenicity of human colon cancer cells. Cancer Res.57, 1569–1574 (1997). CASPubMed Google Scholar
Motokura, T. & Arnold, A. PRAD1/cyclin D1 proto-oncogene: genomic organization, 5′DNA sequence, and sequence of a tumor-specific rearrangement breakpoint. Genes Chromosom. Cancer7, 89–95 (1993). ArticleCAS Google Scholar
Albanese, C. et al. Transforming p21ras mutants and c-ets-2 activate the cyclin D1 promoter through distinguishable regions. J. Biol. Chem.270, 23589–23597 (1995). ArticleCAS Google Scholar
Zhang, T. et al. Concurrent overexpression of cyclin D1 and cyclin-dependent kinase 4 (cdk4) in intestinal adenomas from multiple intestinal neoplasia (Min) mice and human familial adenomatous polyposis patients. Cancer Res.57, 169–175 (1997). CASPubMed Google Scholar
Quelle, D. et al. Overexpression of mouse D-type cyclins accelerates G1 phase in rodent fibroblasts. Genes Dev.7, 1559–1571 (1993). ArticleCAS Google Scholar
Lahti, J. et al. Elimination of cyclin D1 in vertebrate cells leads to an altered cell cycle phenotype, which is rescued by overexpression of murine cyclins D1, D2, or D3 but not by a mutant cyclin D1. J. Biol. Chem.272, 10859–10869 (1997). ArticleCAS Google Scholar