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Toll 样受体多态性与巴西亚马逊地区急性淋巴细胞白血病风险的关联。

Association of Toll-like receptors polymorphisms with the risk of acute lymphoblastic leukemia in the Brazilian Amazon.

机构信息

Programa de Pós-Graduação em Ciências Aplicadas à Hematologia, Universidade do Estado do Amazonas (UEA), Manaus, AM, Brazil.

Diretoria de Ensino e Pesquisa, Fundação Hospitalar de Hematologia e Hemoterapia do Amazonas (HEMOAM), Av. Constantino Nery, 4397, Chapada, Manaus, AM, 69050-001, Brazil.

出版信息

Sci Rep. 2022 Sep 7;12(1):15159. doi: 10.1038/s41598-022-19130-7.

DOI:10.1038/s41598-022-19130-7
PMID:36071076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9452670/
Abstract

Acute lymphoblastic leukemia (ALL) is the most common hematologic malignancy in children in childhood. Single-nucleotide polymorphism (SNPs) in key molecules of the immune system, such as Toll-like receptors (TLRs) and CD14 molecules, are associated with the development of several diseases. However, their role in ALL is unknown. A case-control study was performed with 152 ALL patients and 187 healthy individuals to investigate the role of SNPs in TLRs and the CD14 gene in ALL. In this study, TLR6 C > T rs5743810 [OR: 3.20, 95% CI: 1.11-9.17, p = 0.003) and TLR9 C > T rs187084 (OR: 2.29, 95% CI: 1.23-4.26, p = 0.000) seems to be a risk for development of ALL. In addition, the TLR1 T > G rs5743618 and TLR6 C > T rs5743810 polymorphisms with protection against death (OR: 0.17, 95% IC: 0.04-0.79, p = 0.008; OR: 0.48, 95% IC: 0.24-0.94, p = 0.031, respectively). Our results show that SNPs in TLRs genes may be involved in the pathogenesis of ALL and may influence clinical prognosis; however, further studies are necessary to elucidate the role of TLR1, TLR4, TLR5, TLR6, TLR9 and CD14 polymorphisms in this disease.

摘要

急性淋巴细胞白血病(ALL)是儿童期最常见的血液系统恶性肿瘤。免疫系统关键分子(如 Toll 样受体(TLRs)和 CD14 分子)中的单核苷酸多态性(SNPs)与多种疾病的发生有关。然而,它们在 ALL 中的作用尚不清楚。本病例对照研究纳入了 152 例 ALL 患者和 187 例健康对照,旨在探讨 TLRs 和 CD14 基因中的 SNPs 与 ALL 发病的相关性。在这项研究中,TLR6 C>T rs5743810[比值比(OR):3.20,95%置信区间(CI):1.11-9.17,p=0.003]和 TLR9 C>T rs187084(OR:2.29,95%CI:1.23-4.26,p=0.000)似乎与 ALL 的发病风险相关。此外,TLR1 T>G rs5743618 和 TLR6 C>T rs5743810 多态性与降低死亡风险相关(OR:0.17,95%CI:0.04-0.79,p=0.008;OR:0.48,95%CI:0.24-0.94,p=0.031)。我们的研究结果表明,TLRs 基因中的 SNPs 可能与 ALL 的发病机制有关,并可能影响临床预后;然而,需要进一步的研究来阐明 TLR1、TLR4、TLR5、TLR6、TLR9 和 CD14 多态性在该疾病中的作用。