4.4 Article

The altered expression of ING5 protein is involved in gastric carcinogenesis and subsequent progression

期刊

HUMAN PATHOLOGY
卷 42, 期 1, 页码 25-35

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.humpath.2010.05.024

关键词

Gastric carcinoma; ING5; Pathogenesis; Progression; Prognosis

资金

  1. Shenyang Outstanding Talent Foundation (Shenyang China)
  2. Liaoning BaiQianWan Talents Program (Shenyang China)
  3. Ministry of Personnel Shenyang Science and Technology (Shenyang China) [1091175 1 00]
  4. Scientific Research Foundation for the Returned Overseas Chinese Scholars (Shenyang China) State Education Ministry
  5. Ministry of Education Culture, Sports and Technology (Tokyo Japan) [20659109, 21790624]
  6. Japanese Smoking Research Foundation (Tokyo Japan) Japanese Uehara Memorial Foundation (Tokyo Japan)

向作者/读者索取更多资源

ING5 can interact with p53, thereby inhibiting cell growth and inducing apoptosis To clarify the roles of ING5 in gastric tumorigenesis and progression, its expression was examined by immunohistochemistry on a tissue microarray containing gastric nonneoplastic mucosa (n = 119), dysplasia (n = 50), and carcinomas (n = 429), with its comparison with clinicopathologic parameters of the carcinomas ING5 expression was analyzed in gastric carcinoma tissues and cell lines (MKN28, MKN45, AGS, GT-3 TKB, and KATO III) by Western blot and reverse transcriptase-polymerase chain reaction ING5 protein was found to distribute to the nuclei of gastric carcinoma cells with similar messenger RNA levels An increased expression of ING5 messenger RNA was observed in gastric carcinoma in comparison with paired mucosa (P < 05) Lower expression of nuclear ING5 was detected in gastric dysplasia and carcinoma than that in nonneoplastic mucosa (P < 05) Gastric nonneoplastic mucosa and metastatic carcinoma showed more expression of cytoplasmic ING5 than did gastric carcinoma and dysplasia (P < 05) Nuclear ING5 expression was negatively correlated with tumor size, depth of invasion, lymph node metastasis, and clinicopathologic staging (P < 05), whereas cytoplasmic ING5 was positively associated with depth of invasion, venous invasion, lymph node metastasis and chnicopathologic staging (P < 05) Nuclear ING5 was more expressed in older than younger carcinoma patients (P < 05) There was a higher expression of nuclear ING5 in intestinal-type than diffuse type carcinoma (P < 05), whereas it was the converse for cytoplasmic ING5 (P < 05) Survival analysis indicated that nuclear ING5 was closely linked to favorable prognosis of carcinoma patients (P < 05) albeit not independent It was suggested that aberrant ING5 expression may contribute to pathogenesis, growth, and invasion of gastric carcinomas and could be considered as a promising marker to gauge aggressiveness and prognosis of gastric carcinoma Crown Copyright (C) 2011 Published by Elsevier Inc All rights reserved

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