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CXC 趋化因子受体 5 基因多态性在埃及弥漫性大 B 细胞淋巴瘤患者队列中的研究。

CXC Chemokine Receptor Type 5 Gene Polymorphisms in a Cohort of Egyptian Patients with Diffuse Large B-Cell Lymphoma.

机构信息

Department of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt,

Department of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.

出版信息

Pathobiology. 2021;88(3):211-217. doi: 10.1159/000510456. Epub 2020 Dec 30.

Abstract

BACKGROUND

The chemokine receptor CXCR5 is selectively expressed on B cells; it is involved in lymphocyte homing and the development of normal lymphoid tissue. Its principle ligand is CXCL13 or B lymphocyte chemoattractant. Three polymorphisms in the CXCR5 gene, rs148351692 C/G, rs6421571 C/T, and rs78440425 G/A, have been identified.

OBJECTIVE

To assess the genetic polymorphisms of CXCR5 and evaluate their possible contribution to the susceptibility and response to therapy of diffuse large B-cell lymphoma (DLBCL).

PATIENTS AND METHODS

Fifty DLBCL (not otherwise specified) patients and 50 control subjects were included in this study. CXCR5 genotypes were determined by PCR-RFLP.

RESULTS

Our study revealed that the CXCR5 rs148351692 C/G and rs6421571 C/T gene polymorphisms are associated with an increased risk of developing DLBCL (OR 28.57 [95% CI 8.96-96.56] and 3.45 [1.67-11.83] respectively), while CXCR5 rs78440425 G/A showed no association with the risk of lymphoma. Moreover, the double and triple combined gene polymorphisms are associated with an increased risk of developing DLBCL of approximately 120-fold and 105-fold, respectively. CXCR5 gene polymorphisms had no significant impact on disease outcome or response to therapy.

CONCLUSIONS

CXCR5 gene polymorphisms could be considered a potential risk factor for the development of DLBCL.

摘要

背景

趋化因子受体 CXCR5 选择性地表达于 B 细胞;它参与淋巴细胞归巢和正常淋巴组织的发育。其主要配体是 CXCL13 或 B 细胞趋化因子。CXCR5 基因中有三个多态性,rs148351692C/G、rs6421571C/T 和 rs78440425G/A。

目的

评估 CXCR5 的遗传多态性,并评估其对弥漫性大 B 细胞淋巴瘤(DLBCL)易感性和治疗反应的可能贡献。

患者和方法

本研究纳入了 50 例 DLBCL(非特指型)患者和 50 名对照。通过 PCR-RFLP 确定 CXCR5 基因型。

结果

我们的研究表明,CXCR5 rs148351692C/G 和 rs6421571C/T 基因多态性与 DLBCL 的发病风险增加相关(OR 分别为 28.57 [95%CI 8.96-96.56]和 3.45 [1.67-11.83]),而 CXCR5 rs78440425G/A 与淋巴瘤的发病风险无关。此外,双和三重联合基因多态性与 DLBCL 的发病风险增加分别约 120 倍和 105 倍相关。CXCR5 基因多态性对疾病结局或治疗反应无显著影响。

结论

CXCR5 基因多态性可被视为 DLBCL 发生的潜在危险因素。

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