Literature DB >> 9771480

Beta- and gamma-catenin expression in thyroid carcinomas.

A Cerrato1, F Fulciniti, A Avallone, G Benincasa, L Palombini, M Grieco.   

Abstract

Cadherins are calcium-dependent cell-cell adhesion molecules whose intracellular domain forms a complex with proteins required for their function, called catenins. Down-regulation of cadherins has frequently been detected in many types of human carcinomas, being associated with tumour progression. The present study investigates the immunohistochemical expression of E-cadherin and beta- and gamma-catenin in 27 human thyroid carcinomas. E-cadherin immunoreactivity was found to be decreased at cell-cell contacts in 8/15 (53 per cent) papillary, 5/7 (71 per cent) follicular, and 5/5 (100 per cent) anaplastic carcinomas. Beta-catenin membrane localization was found to be decreased in 6/15 (40 per cent) papillary, 2/7 (28 per cent) follicular, and 5/5 (100 per cent) anaplastic carcinomas. Gamma-catenin expression was partially or totally lost in 13/15 (86 per cent) papillary, 6/7 (85 per cent) follicular, and 5/5 (100 per cent) anaplastic carcinomas. A normal pattern of expression for these three molecules was observed in areas of normal tissue in each sample. These data indicate that in addition to E-cadherin, catenins are also down-regulated at cell-cell junctions in thyroid tumours and could represent potentially useful differentiation and/or transformation markers. The high frequency of alterations of gamma-catenin expression found in thyroid carcinomas suggests an important role for this gene product in thyroid carcinogenesis.

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Year:  1998        PMID: 9771480     DOI: 10.1002/(SICI)1096-9896(199807)185:3<267::AID-PATH113>3.0.CO;2-C

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  16 in total

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2.  Beta-catenin dysregulation in thyroid neoplasms: down-regulation, aberrant nuclear expression, and CTNNB1 exon 3 mutations are markers for aggressive tumor phenotypes and poor prognosis.

Authors:  G Garcia-Rostan; R L Camp; A Herrero; M L Carcangiu; D L Rimm; G Tallini
Journal:  Am J Pathol       Date:  2001-03       Impact factor: 4.307

Review 3.  The cadherin-catenin superfamily in endocrine tumors.

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Journal:  Endocr Pathol       Date:  2001       Impact factor: 3.943

4.  Analysis of beta-catenin mutations and alpha-, beta-, and gamma-catenin expression in normal and neoplastic human pituitary tissues.

Authors:  V Tziortzioti; K H Ruebel; T Kuroki; L Jin; B W Scheithauer; R V Lloyd
Journal:  Endocr Pathol       Date:  2001       Impact factor: 3.943

Review 5.  Molecular pathobiology of thyroid neoplasms.

Authors:  Giovanni Tallini
Journal:  Endocr Pathol       Date:  2002       Impact factor: 3.943

6.  Immunoexpression of HBME-1, high molecular weight cytokeratin, cytokeratin 19, thyroid transcription factor-1, and E-cadherin in thyroid carcinomas.

Authors:  Yoon-La Choi; Mi Kyung Kim; Jin-Won Suh; Joungho Han; Jung Han Kim; Jung Hyun Yang; Seok Jin Nam
Journal:  J Korean Med Sci       Date:  2005-10       Impact factor: 2.153

7.  Snail family transcription factors are implicated in thyroid carcinogenesis.

Authors:  Robert G Hardy; Carolina Vicente-Dueñas; Ines González-Herrero; Catriona Anderson; Teresa Flores; Sharon Hughes; Chris Tselepis; James A Ross; Isidro Sánchez-García
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8.  Nuclear Accumulation of B-Catenin in Human Endocrine Tumors: Association with Ki-67 (MIB-1) Proliferative Activity.

Authors:  Shuho Semba; Ryoko Kusumi; Takuya Moriya; Hironobu Sasano
Journal:  Endocr Pathol       Date:  2000       Impact factor: 3.943

9.  Adhesion molecules and p16 expression in endocervical adenocarcinoma.

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Journal:  Virchows Arch       Date:  2009-08-13       Impact factor: 4.064

10.  Immunohistochemical detection of E-cadherin, alpha- and beta-catenins in papillary thyroid carcinoma.

Authors:  Y Kapran; N Ozbey; S Molvalilar; E Sencer; F Dizdaroğlu; S Ozarmağan
Journal:  J Endocrinol Invest       Date:  2002 Jul-Aug       Impact factor: 4.256

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