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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Immunoexpression of DIABLO, AIF and Cytochrome c in Gastric Adenocarcinoma Assessed by Tissue Microarray

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Author(s):
Da Silva, Larissa Comparini [1] ; Forones, Nora Manoukian [2] ; Ribeiro, Daniel Araki [3] ; Miki Ihara, Silvia Sauli [1] ; Gomes, Thiago Simao [1] ; Neto, Ricardo Artigiani [1] ; Fujiyama Oshima, Celina Tizuko [1]
Total Authors: 7
Affiliation:
[1] Univ Fed Sao Paulo, UNIFESP, Dept Pathol, BR-11060001 Santos, SP - Brazil
[2] Univ Fed Sao Paulo, UNIFESP, Dept Med, Div Gastroenterol, BR-11060001 Santos, SP - Brazil
[3] Univ Fed Sao Paulo, UNIFESP, Dept Biosci, BR-11060001 Santos, SP - Brazil
Total Affiliations: 3
Document type: Journal article
Source: ANTICANCER RESEARCH; v. 33, n. 2, p. 647-653, FEB 2013.
Web of Science Citations: 2
Abstract

The aim of this study was to analyze the immunoexpressioh of (Smac) DIABLO, AIF, cytochrome c, Ki-67 and cleaved caspase-3 in gastric cancer. A tissue microarray (TMA) paraffin block was constructed using gastric adenocarcinoma tissue and adjacent normal adjacent mucosa from 87 patients who had not previously undergone radiotherapy or chemotherapy. Immunohistochemistry was used to evaluate the protein levels. Samples were positive for (Smac) DIABLO in 37 (45.6%) and 37 (46.8%), for AIF in 31 (36.9%) and 36 (45.6%), for cytochrome c in 60 (68.9%) and 44 (54.4%), for Ki-67 in 63 (72.4%) and 52 (61.9%) and for cleaved caspase-3 in 21 (24.1%) and 3 (3.4%) cases of tumor and adjacent normal tissues, respectively. Our results suggest that increased expression of Ki-67 and cleaved caspase-3 could contribute to carcinogenesis. The expression of these proteins indicates an attempt of cells to maintain tissue homeostasis. (AU)

FAPESP's process: 10/15764-8 - Immuno-expression of Smac/Diablo, AIF, cytochrome c, cleaved caspase 3 and Ki-67 in gastric cancer tissue by tissue micro array (TMA)
Grantee:Celina Tizuko Fujiyama Oshima
Support Opportunities: Regular Research Grants