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CTLA-4 +49A>G 多态性与结直肠癌的风险相关,但与进展无关。

CTLA-4 +49A>G polymorphism is associated with the risk but not with the progression of colorectal cancer in Chinese.

机构信息

Department of Laboratory Medicine, Eastern Hepatobiliary Hospital, Second Military Medical University, Shanghai, China.

出版信息

Int J Colorectal Dis. 2010 Jan;25(1):39-45. doi: 10.1007/s00384-009-0806-z. Epub 2009 Sep 29.

DOI:10.1007/s00384-009-0806-z
PMID:19787358
Abstract

PURPOSE

Colorectal cancer (CRC) is one of the most common malignancies in the world and a multipathway disease. Cytotoxic T-lymphocyte antigen-4 (CTLA-4) is a potent immunoregulatory molecule that suppresses antitumor response by down-regulating T-cell activation. The most studied +49A>G polymorphism of CTLA-4 gene has been associated with several autoimmune or cancer diseases. Our aim was to investigate the association between this genetic variant and the risk as well as progression of colorectal cancer in Chinese.

METHODS

We conducted a case-control study of 124 colorectal cancer cases and 407 healthy controls. DNA was extracted from blood specimens, and +49A>G polymorphism in the CTLA-4 gene was genotyped by polymerase chain reaction-ligation detection reaction (PCR-LDR).

RESULTS

In our study group, the frequency of AG or GG or carrying at least one G allele at position +49 was significantly different in colorectal cancer patients and the control group, indicating that the risk of CRC was significantly higher among subjects with the AG or GG genotype or carrying at least one G allele at position +49 than among the subjects with the AA genotype. However, we observed no association between CTLA-4 +49A>G polymorphism and the progression of CRC. Interestingly, the CTLA-4 +49A allele was in non-significantly higher numbers in CRC patients with distant metastasis.

CONCLUSIONS

Our results suggested that CTLA-4 +49A>G polymorphism was associated with an increased risk of colorectal cancer, but this polymorphism did not play an important role in the progression of CRC in Chinese.

摘要

目的

结直肠癌(CRC)是世界上最常见的恶性肿瘤之一,也是一种多途径疾病。细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)是一种有效的免疫调节分子,通过下调 T 细胞激活来抑制抗肿瘤反应。CTLA-4 基因最受研究的+49A>G 多态性与多种自身免疫或癌症疾病有关。我们的目的是研究这种遗传变异与中国人群结直肠癌的风险和进展之间的关系。

方法

我们进行了一项病例对照研究,纳入了 124 例结直肠癌患者和 407 名健康对照者。从血标本中提取 DNA,采用聚合酶链反应-连接酶检测反应(PCR-LDR)检测 CTLA-4 基因的+49A>G 多态性。

结果

在我们的研究组中,结直肠癌患者和对照组之间 CTLA-4 基因+49 位的 AG 或 GG 或至少携带一个 G 等位基因的频率存在显著差异,表明与 AA 基因型相比,AG 或 GG 基因型或至少携带一个 G 等位基因的个体患 CRC 的风险显著更高。然而,我们未观察到 CTLA-4+49A>G 多态性与 CRC 进展之间存在关联。有趣的是,远处转移的 CRC 患者中 CTLA-4+49A 等位基因的数量呈非显著性增加。

结论

我们的结果表明,CTLA-4+49A>G 多态性与结直肠癌的风险增加有关,但这种多态性在中国人群中对 CRC 的进展没有重要作用。

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