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CTLA-4 基因多态性与中国东北汉族女性散发性乳腺癌风险及临床特征的相关性。

Association of CTLA-4 gene polymorphisms with sporadic breast cancer risk and clinical features in Han women of northeast China.

机构信息

Department of Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin 150081, China.

出版信息

Mol Cell Biochem. 2012 May;364(1-2):283-90. doi: 10.1007/s11010-012-1228-8. Epub 2012 Jan 17.

Abstract

Cytotoxic T lymphocyte antigen-4 (CTLA-4) is an inhibitory molecule that plays a pivotal role in downregulating T-cell mediated immune responses. To determine the role of CTLA-4 in tumor immunity, and to validate previous results as well, we investigated four tag single nucleotide polymorphisms (SNPs) of CTLA-4 in a relatively large Chinese Han cohort from northeastern China. Genotypes were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 581 patients and 566 age-matched controls. Our data indicated that compared with the common genotype and allele of each SNP, the -1722 CC genotype and C allele showed an increased risk of breast cancer (P = 0.030, odds ratio (OR) = 1.457, 95% confidence internal (CI) 1.036-2.051; P = 0.024, OR = 1.214, 95% CI 1.026-1.436, respectively). The -1661 GG genotype and G allele were also associated with an increased risk of breast cancer (P = 0.018, OR = 1.396, 95% CI 1.058-1.843; P = 0.013, OR = 1.353, 95% CI 1.066-1.717, respectively). In the haplotype analysis, the CAAA haplotype showed a higher frequency in cases (P = 0.004), and this association remained significant after correcting the P value for multiple testing. Associations were shown between the SNPs of CTLA-4 and lymph node metastasis, estrogen receptor (ER), progesterone receptor (PR) and P53 statuses. These results indicate that some SNPs in the CTLA-4 gene may affect the risk of breast cancer and show that some SNPs are associated with breast cancer characteristics in Han women in northeastern China.

摘要

细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)是一种抑制性分子,在下调 T 细胞介导的免疫反应中起着关键作用。为了确定 CTLA-4 在肿瘤免疫中的作用,并验证以前的结果,我们在中国东北地区的一个较大的汉族队列中研究了 CTLA-4 的四个标签单核苷酸多态性(SNP)。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)在 581 名患者和 566 名年龄匹配的对照中确定基因型。我们的数据表明,与每个 SNP 的常见基因型和等位基因相比,-1722 CC 基因型和 C 等位基因显示出乳腺癌的风险增加(P=0.030,优势比(OR)=1.457,95%置信区间(CI)1.036-2.051;P=0.024,OR=1.214,95%CI 1.026-1.436)。-1661 GG 基因型和 G 等位基因也与乳腺癌风险增加相关(P=0.018,OR=1.396,95%CI 1.058-1.843;P=0.013,OR=1.353,95%CI 1.066-1.717)。在单体型分析中,CAAA 单体型在病例中出现频率更高(P=0.004),并且在对多重检验校正 P 值后,这种关联仍然显著。CTLA-4 基因的 SNP 与淋巴结转移、雌激素受体(ER)、孕激素受体(PR)和 P53 状态之间存在关联。这些结果表明 CTLA-4 基因中的一些 SNP 可能影响乳腺癌的风险,并表明一些 SNP 与中国东北地区汉族女性的乳腺癌特征有关。

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