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PPARγ 及其共激活因子 PGC-1 的表达下调与胃癌的发生和 Lauren 分型有关。

Down-regulated expressions of PPARγ and its coactivator PGC-1 are related to gastric carcinogenesis and Lauren's classification in gastric carcinoma.

机构信息

Department of Gastrointestinal Tumor Pathology of Cancer Institute and General Surgery Institute, the First Hospital of China Medical University, Shenyang 110001, China.

出版信息

Chin J Cancer Res. 2013 Dec;25(6):704-14. doi: 10.3978/j.issn.1000-9604.2013.11.11.

Abstract

OBJECTIVE

To explore the relationship between peroxisome proliferator activated receptor-gamma (PPARγ) and peroxisome proliferator-activated receptor-gamma coactivator-1 (PGC-1) expression in gastric carcinoma (GC), and analyze their correlations with clinicopathological features and clinical outcomes of patients.

METHODS

The two-step immunohistochemical method was used to detect the expression of PPARγ and PGC-1 in 179 cases of GC, and 108 cases of matched normal gastric mucosa. Besides, 16 cases of fresh GC specimens and corresponding normal gastric mucosa were detected for PGC-1 expression with Western blotting.

RESULTS

The positive rates of PPARγ and PGC-1 expression were significantly lower in GC (54.75%, 49.16%) than in normal gastric mucosa (70.37%, 71.30%), respectively (P<0.05). The decreased expression of PGC-1 in GC was confirmed in our Western blot analysis (P=0.004). PPARγ and PGC-1 expressions were related to Lauren's types of GC (P<0.05). Positive correlation was found between PPARγ and PGC-1 expression in GC (rk=0.422, P<0.001). The survival time of PPARγ negative and positive patients was 36.6±3.0 vs. 38.5±2.7 months, and no statistical difference was found between the 5-year survival rates of two groups (34.4% vs. 44.1%, P=0.522, log-rank test); the survival time of PGC-1 negative and positive patients was 36.2±2.8 vs. 39.9±2.9 months, while no statistical difference was found between the 5-year survival rates of the two groups (32.0% vs. 48.2%, P=0.462, log-rank test).

CONCLUSIONS

Decreased expression of PPARγ and PGC-1 in GC was related to the Lauren's classification. Their expressions in GC were positively correlated, indicating that their functions in gastric carcinogenesis may be closely related.

摘要

目的

探讨过氧化物酶体增殖物激活受体-γ(PPARγ)和过氧化物酶体增殖物激活受体-γ共激活因子-1(PGC-1)在胃癌(GC)中的表达关系,并分析其与患者临床病理特征及临床结局的关系。

方法

采用两步免疫组化法检测 179 例 GC 及 108 例配对正常胃黏膜组织中 PPARγ和 PGC-1 的表达,并用 Western blot 法检测 16 例新鲜 GC 标本及其相应正常胃黏膜组织中 PGC-1 的表达。

结果

GC 中 PPARγ和 PGC-1 的阳性表达率分别为 54.75%(101/186)和 49.16%(92/186),明显低于相应正常胃黏膜组织的 70.37%(79/112)和 71.30%(80/112)(P<0.05)。Western blot 分析也证实 GC 中 PGC-1 的表达下调(P=0.004)。PPARγ和 PGC-1 的表达与 GC 的 Lauren 分型有关(P<0.05)。GC 中 PPARγ和 PGC-1 的表达呈正相关(rk=0.422,P<0.001)。PPARγ阴性和阳性患者的生存时间分别为 36.6±3.0 个月和 38.5±2.7 个月,两组 5 年生存率差异无统计学意义(34.4%比 44.1%,P=0.522,log-rank 检验);PGC-1 阴性和阳性患者的生存时间分别为 36.2±2.8 个月和 39.9±2.9 个月,两组 5 年生存率差异无统计学意义(32.0%比 48.2%,P=0.462,log-rank 检验)。

结论

GC 中 PPARγ和 PGC-1 的表达下调与 Lauren 分型有关。GC 中它们的表达呈正相关,提示它们在胃癌发生中的作用可能密切相关。

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