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SIRT1在胃癌组织中表达及对患者预后的影响

丁竞竞 何松 张建兵 吴徐明 陈颜夙 夏晓伟 王守宇 强福林 周建伟

南京医科大学学报(自然科学版)2011,Vol.31Issue(8):1142-1147,6.
南京医科大学学报(自然科学版)2011,Vol.31Issue(8):1142-1147,6.

SIRT1在胃癌组织中表达及对患者预后的影响

Expressions of SIRT1 as prognostic biomarker on resectable gastric cancer patient

丁竞竞 1何松 2张建兵 2吴徐明 2陈颜夙 1夏晓伟 1王守宇 1强福林 2周建伟1

作者信息

  • 1. 南京医科大学公共卫生学院分子毒理实验室,江苏南京210029
  • 2. 南通市肿瘤医院病理科,江苏南通226361
  • 折叠

摘要

Abstract

Objective:To investigate the SIRT1 expressions in gastric cancer tissue and the potential association with clinicopathological characteristics and prognosis of the patients. Methods:The clinicopathological and survival information of the 142 cases who underwent radical gastrectomy at Nantong Cancer Hospital from January 1990 to December 1995, was collected to establish a combined database. The tissue microarray was made from the paraffin embed gastric cancer tissues and corresponding adjacent nontumoral gastric tissues from 142 resectable patients. Expressions of SIRT1 were evaluated by a semi-quantitative immunoreactivity scoring (IRS) procedure. The correlations between the expressions of the SIRT1 and clinicopathological as well as survival characteristics of patients were further analyzed. Results:Expressions of SIRT1 were significantly lower in cancer lesions than in adjacent noncancerous tissues. Low tumoral SIRT1 expression was associated with depth of invasion,presence of lymph node metastasis,high pTNM stage and poor differentiation,respectively. Importantly,reduced SIRT1 expressions in cancerous tissues were significantly correlated with shorter overall survival (OS) in patients (HR = 0.205,95%CI:0.124~0.339,P < 0.001). Conclusion: SIRT1 might be a novel biomarker for evaluating progression and prognosis of resectable gastric cancer patients.

关键词

SIRT1;胃癌;预后;生物标志物

Key words

SIRT1/gastric cancer/prognosis/biomarker

分类

生物科学

引用本文复制引用

丁竞竞,何松,张建兵,吴徐明,陈颜夙,夏晓伟,王守宇,强福林,周建伟..SIRT1在胃癌组织中表达及对患者预后的影响[J].南京医科大学学报(自然科学版),2011,31(8):1142-1147,6.

基金项目

国家自然科学基金重点项目资助(30930080) (30930080)

南京医科大学学报(自然科学版)

OA北大核心CSCDCSTPCD

1007-4368

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