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T 细胞调节基因多态性与口腔鳞状细胞癌的关联。

Association of T-cell regulatory gene polymorphisms with oral squamous cell carcinoma.

机构信息

Department of Oral and Maxillofacial Surgery, University Medical Centre of the Johannes Gutenberg University, Mainz, Germany.

出版信息

Oral Oncol. 2010 Jul;46(7):543-8. doi: 10.1016/j.oraloncology.2010.03.025.

Abstract

Costimulatory molecules have complementary effects on T-cell activation and their balance may control the development of oral cancer. The aim of this study was to determine the relevance of cytotoxic T-lymphocyte antigen 4 (CTLA-4), CD28 and inducible costimulator (ICOS) polymorphisms in oral squamous cell carcinoma (OSCC). Genotyping for CTLA-4 (-1661 A/G and +49 A/G), CD28 (0 C/G and +3160 G/T) and ICOS (+637 A/C and +1599 C/T) was performed in the 83 patients with OSCC, compared to the 40 unrelated healthy volunteers as controls. The genotype CTLA-4 -1661 was significantly different between the patient group and the control group. The allele CTLA-4 -1661 G was significantly found more frequent in patients with OSCC (p=0.001). In bivariate analysis, noticeable differences between OSCC and controls were seen. The combinations CTLA-4 -1661 G/G and CTLA-4 +49 A/G, ICOS +1559 C/T and ICOS +1559 C/C each with CTLA-4 -1661 G/G, ICOS +637 C/C and ICOS +637 A/C each with CTLA-4 -1661, CTLA-4 -1661 A/G and ICOS +637 C/C, CD28 +3160 G/T and CTLA-4 -1661 A/A and CD28 +3160 G/T and CTLA-4 -1661 A/G were seen in the patient group only. Especially the polymorphisms of the CTLA-4 -1661-genotype - alone and in combination with other T cell regulator polymorphisms - seem to be possible predisposing factors for OSCC. Therefore, they might be future targets for a primary prophylaxis or an individualised therapy.

摘要

共刺激分子对 T 细胞的激活有互补作用,其平衡可能控制口腔癌的发展。本研究的目的是确定细胞毒性 T 淋巴细胞抗原 4(CTLA-4)、CD28 和诱导共刺激分子(ICOS)多态性在口腔鳞状细胞癌(OSCC)中的相关性。对 83 例 OSCC 患者和 40 名无关的健康志愿者进行 CTLA-4(-1661A/G 和 +49A/G)、CD28(0C/G 和 +3160G/T)和 ICOS(+637A/C 和 +1599C/T)的基因分型。CTLA-4-1661 基因型在患者组和对照组之间有显著差异。等位基因 CTLA-4-1661G 在 OSCC 患者中明显更常见(p=0.001)。在双变量分析中,OSCC 组和对照组之间有显著差异。组合 CTLA-4-1661G/G 和 CTLA-4+49A/G、ICOS+1559C/T 和 ICOS+1559C/C 各与 CTLA-4-1661G/G、ICOS+637C/C 和 ICOS+637A/C 各与 CTLA-4-1661、CTLA-4-1661A/G 和 ICOS+637C/C、CD28+3160G/T 和 CTLA-4-1661A/A 和 CD28+3160G/T 和 CTLA-4-1661A/G 仅在患者组中可见。特别是 CTLA-4-1661 基因型的多态性-单独存在或与其他 T 细胞调节因子的多态性结合-似乎是 OSCC 的可能易感因素。因此,它们可能是初级预防或个体化治疗的未来靶点。

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