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Prognostic and Clinical Value of Sirt1 Expression in Gastric Cancer:A Systematic Meta-Analysis 被引量:3

Prognostic and Clinical Value of Sirt1 Expression in Gastric Cancer:A Systematic Meta-Analysis
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摘要 Many studies have reported that the expression of silent information regulator 1(Sirt1) is associated with the clinical features and prognosis of patients with gastric cancer, but the exact function remains controversial. We conducted this study to illustrate the clinical and prognostic value of Sirt1 in gastric cancer. The related publications before December 2015 were searched in the databases including Pubmed, Cochrane Library, Embase and China National Knowledge Infrastructure(CNKI). The studies were included and excluded according to the inclusion criteria and exclusion criteria. The 3- and 5-year overall survival(OS) and clinical features such as age, T stage, N stage and differentiation were analyzed by software Rev Man 5.3. A total of 1650 patients in 7 studies were included according to the inclusion criteria and exclusion criteria. The high expression of Sirt1 was found in 58.4% cases by immunohistochemistry. High expression of Sirt1 was closely linked with the 3-year OS(OR=0.25, 95% CI: 0.16–0.39, P0.00001, fixed), patient's age(≥60 years old vs. 〈60 years old; OR=1.43, 95% CI: 1.06–1.93, P=0.02, fixed), T stage(T3+T4 vs. T1+T2; OR=1.45, 95% CI: 1.08–1.94, P=0.01, fixed), N stage(N1+N2+N3 vs. N0; OR=3.47, 95% CI: 2.39–5.05, P〈0.00001, fixed) and tumor differentiation(G1+G2 vs. G3; OR=0.50, 95% CI: 0.35–0.69, P〈0.0001, fixed). Nevertheless, it seemed that high expression of Sirt1 was not associated with 5-year OS(OR=0.44, 95% CI: 0.15–1.28, P=0.13, random). It was suggested that the high expression of Sirt1 implies a poor prognosis of gastric cancer patients in a relatively short period(3 years), but not in a long time(≥5 years). The expression of Sirt1 is also linked with patients' age, T stage, N stage and tumor differentiation. Many studies have reported that the expression of silent information regulator 1(Sirt1) is associated with the clinical features and prognosis of patients with gastric cancer, but the exact function remains controversial. We conducted this study to illustrate the clinical and prognostic value of Sirt1 in gastric cancer. The related publications before December 2015 were searched in the databases including Pubmed, Cochrane Library, Embase and China National Knowledge Infrastructure(CNKI). The studies were included and excluded according to the inclusion criteria and exclusion criteria. The 3- and 5-year overall survival(OS) and clinical features such as age, T stage, N stage and differentiation were analyzed by software Rev Man 5.3. A total of 1650 patients in 7 studies were included according to the inclusion criteria and exclusion criteria. The high expression of Sirt1 was found in 58.4% cases by immunohistochemistry. High expression of Sirt1 was closely linked with the 3-year OS(OR=0.25, 95% CI: 0.16–0.39, P0.00001, fixed), patient's age(≥60 years old vs. 〈60 years old; OR=1.43, 95% CI: 1.06–1.93, P=0.02, fixed), T stage(T3+T4 vs. T1+T2; OR=1.45, 95% CI: 1.08–1.94, P=0.01, fixed), N stage(N1+N2+N3 vs. N0; OR=3.47, 95% CI: 2.39–5.05, P〈0.00001, fixed) and tumor differentiation(G1+G2 vs. G3; OR=0.50, 95% CI: 0.35–0.69, P〈0.0001, fixed). Nevertheless, it seemed that high expression of Sirt1 was not associated with 5-year OS(OR=0.44, 95% CI: 0.15–1.28, P=0.13, random). It was suggested that the high expression of Sirt1 implies a poor prognosis of gastric cancer patients in a relatively short period(3 years), but not in a long time(≥5 years). The expression of Sirt1 is also linked with patients' age, T stage, N stage and tumor differentiation.
出处 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2016年第2期278-284,共7页 华中科技大学学报(医学英德文版)
基金 supported by the National Natural Science Foundation of China(Nos.81271199 and 81470789)
关键词 gastric cancer silent information regulator 1 clinicopathological characteristics PROGNOSIS gastric cancer silent information regulator 1 clinicopathological characteristics prognosis
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