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Nuclear beta-catenin

Fischer AN, Fnchs E, Mikula M, Huber H, Beug H, Mikulits W (2006). PDGF essentially links TGF beta signaling to nuclear beta-catenin accumulation in hepatocellular carcinoma progression. Oncogene [Epub ahead of print]. [Pg.133]

Bhattacharya B, Dilworth HP, lacobtrzio-Donahue C, et al. Nuclear beta-catenin expression distingirishes deep fibromatosis from other benign and malignant fibroblastic and myofibroblastic lesions. Am J Surg Pathol. 2005 29 653-659. [Pg.130]

Adenocarcinomas of urinary bladder (urachal origin) are CDX2-I- but are also positive for thrombomodulin and CK7, whereas colorectal carcinomas are negative with thrombomodulin and CK7 and have nuclear beta-catenin expression. [Pg.232]

Ng TL, Gown AM, Barry TS, et al. Nuclear beta-catenin in mesenchymal tumors. Mod Pathol. 2005 18 68-74. [Pg.539]

Jung CK, Jung JH, Lee A, et al. Diagnostic use of nuclear beta-catenin expression for the assessment of endometrial stromal tumors. Mod Pathol. 2008 21 756-763. [Pg.751]

Yamazaki K, Hanami K, Nagao T, Asoh A, Sugano I, Ishida Y. Increased cyclinDl expression in cancer of the ampula of Vater relevance to nuclear beta-catenin accumulation and K-ras gene mutation. Mol Pathol. 2003 56 336-41. [Pg.694]

Stucke VM, Corses D, Hofmann F (2008) DEAD-box RNA helicase p68 is not required for nuclear translocation of beta-catenin in colon cancer cells. Cell Cycle 7 830-832... [Pg.12]

Persad S, Troussard AA, McPhee TR, Mulholland DJ, Dedhar S. Tumor suppressor PTEN inhibits nuclear accumulation of beta-catenin and T cell/lymphoid enhancer factor 1-mediated transcriptional activation. J. Cell. Biol. 2001 153 1161-1174. Yang Y, Guo L, Blattner SM, Mundel P, Kretzler M, Wu C. Formation and phosphorylation of the PINCH-l-integrin linked kinase-alpha-parvin complex are important for regulation of renal glomerular podoc)4e adhesion, architecture, and survival. J. Am. Soc. Nephrol. 2005 16 1966-1976. [Pg.782]

FIGURE 4.2 Nuclear labeling for beta-catenin is typical of deep fibromatosis. [Pg.97]

Eew studies have been done on the molecular features of gastrointestinal endocrine tumors. Allelic loss of llq has been detected in GI endocrine tumors associated with MENl, and LOH of 1 Iq is also present in a subset of sporadic GI endocrine tumors. Mutations of the MENl gene are present in approximately 30% of sporadic gastrinomas and in occasional midgut and hindgut endocrine tumors. In contrast to pancreatic endocrine tumors, the CpG island methylator phenotype is frequent in GI endocrine tumors. Beta-catenin exon 3 mutations are relatively common (38%) in these tumors, and up to 80% of the tumors show nuclear and cytoplasmic localization of the corresponding protein. Other studies, however, reported absence of exon 3 mutations, but nuclear f5-catenin was found in 30% of cases. In contrast, extra-GI endocrine tumors were negative for nuclear f5-catenin. [Pg.321]

Garcia-Rostan G, Camp RL, Herreo A, et al. Beta catenin dys-regulation in thyroid neoplasms Down regrrlation, aberrant nuclear expression, and CTNNBl exon 3 mutations are markers for aggressive trrmor phenotypes and poor prognosis. Am J Pathol. 2001 158 987-996. [Pg.332]

Su MC, Wang CC, Chen CC, et al. Nuclear translocation of beta-catenin and APC mutation in gastrointestinal carcinoid tumor. Ann Surg Oncol. 2006 13 1604-1609. [Pg.336]

SOLITARY FIBROUS TUMOR AND PSEUDOTUMOR Solitary fibrous tumors infrequently arise in the upper abdomen and mesentery.350.375-377 They are positive with CD34, CD99, and smooth muscle actin but do not stain with CD 117.350.368,378 Also, approximately 25% of solitary fibrous tumors stain with beta-catenin in a nuclear pat-tern.3 3 Nodular fibrous pseudotumors are rare lesions in this location. They share strong GDI 17 reactivity with GISTs however, they are morphologically distinct from GISTs. [Pg.525]

Saito T, Oda Y, Tanaka K, et al. beta-catenin nuclear expression correlates with cyclin D1 overexpression in sporadic desmoid tumours. J Pathol. 2001 195 222-228. [Pg.540]

Tanaka Y, Kato K, Notohara K, et al. Significance of aberrant (cytoplasmic/nuclear) expression of beta-catenin in pancreatoblastoma. J Pathol. 2003 199 185-190. [Pg.583]

Kim MJ, Jang SJ, Yu E. Loss of E-cadherin and cytoplasmic-nuclear expression of beta-catenin are the most useful immuno-profiles in the diagnosis of solid-pseudopapillary neoplasm of the pancreas. Hum Pathol. 2008 39 251-258. [Pg.583]

Haydon RC, Deyrup A, Ishikawa A, et al. Cytoplasmic and/or nuclear accumulation of the beta-catenin protein is a frequent event in human osteosarcoma. Int J Cancer. 2002 102 338-342. [Pg.689]

Saegusa M, Hamano M, Kuwata T, et al. Up-regulation and nuclear localization of beta-catenin in endometrial carcinoma in response to progesterone therapy. Cancer Sci. 2003 94 103-... [Pg.749]

Williams, J.L., Nath, N., Chen, J., Hundley, T.R., Gao, J., Kopelovich, L., Kashfi, K., and Rigas, B. (2003). Growth inhibition of human colon cancer cells by nitric oxide (no)-donating aspirin is associated with cyclooxygena.se-2 induction and beta-catenin/t-cell factor signahng, nuclear factor-kappab, and no synthase 2 inhibition Implications for chemoprevention. Cancer Res. 63, 7613-7618. [Pg.131]


See other pages where Nuclear beta-catenin is mentioned: [Pg.87]    [Pg.97]    [Pg.231]    [Pg.345]    [Pg.683]    [Pg.87]    [Pg.97]    [Pg.231]    [Pg.345]    [Pg.683]    [Pg.299]    [Pg.243]    [Pg.231]    [Pg.304]    [Pg.525]    [Pg.554]    [Pg.247]    [Pg.2194]    [Pg.2207]    [Pg.254]   
See also in sourсe #XX -- [ Pg.97 ]




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