Impact of NLRP3 gene polymorphisms (rs10754558 and rs10733113) on HPV infection and cervical cancer in southern Chinese population.

IF 3.1 2区 医学 Q3 IMMUNOLOGY Infectious Agents and Cancer Pub Date : 2023-10-26 DOI:10.1186/s13027-023-00529-4
Qingchun Lu, Xiaoxia Lao, Jinghua Gan, Ping Du, Yingpei Zhou, Wenzheng Nong, Zhige Yang
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Abstract

Objective: Mutations in the NLRP3gene have previously been linked to certain forms of cancer, but there have not been any specific studies examining the association between NLRP3 polymorphisms and cervical cancer (CC). This study was therefore designed to investigate the effect of NLRP3 gene polymorphisms on HPV infection and cervical cancer in southern Chinese population.

Methods: Multiplex PCR and next-generation sequencing approaches were used to assess the NLRP3 rs10754558 and rs10733113 polymorphisms in 404 cervical lesion patients, including 227 diagnosed with CC and 177 diagnosed with cervical intraepithelial neoplasia(CIN), with 419 healthy female controls being included for comparison. Correlations between the rs10754558 and rs10733113 genotypes and alleles in these patients and CC and CIN were then analyzed.

Results: No correlations were found between NLRP3 rs10754558 and rs10733113 and human papillomavirus(HPV) infection status. Relative to the healthy control group, the NLRP3 rs10754558 GG genotype, CG + GG genotype, and G allele frequencies were significantly increased among patients with cervical lesions (CC and CIN) (OR = 1.815,P = 0.013;OR = 1.383, P = 0.026; OR = 1.284, P = 0.014,respectively), whereas no such differences were observed for rs10733113. A higher cervical lesion risk was detected for patients over the age of 45 exhibiting the rs10754558 GG genotype (OR = 1.848, P = 0.040). Additionally, the risk of CC was elevated in patients with the rs10754558 GG genotype or the G allele relative to patients with the CC genotype or the C allele(OR = 1.830, P = 0.029; OR = 1.281, P = 0.039). The rs10733113 genotypes or alleles were not significantly associated with CC risk (P > 0.05). No association between rs10754558 and rs10733113 genotypes and CC patient clinicopathological features were observed (P > 0.05). Serum NLRP3, IL-1β, and IL-18 levels were significantly elevated in CC patients relative to healthy controls(P < 0.05). Relative to the CC genotype, CC patients harboring the rs10754558 GG genotype exhibited significantly elevated IL-1β and IL-18 levels(P < 0.05).

Conclusion: The rs10754558 polymorphism in the NLRP3 gene may contribute to an elevated risk of CC, although it is not significantly correlated with HPV infection and CC progression.

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NLRP3基因多态性(rs10754558和rs10733113)对中国南方人群HPV感染和宫颈癌症的影响。
目的:NLRP3基因突变以前与某些形式的癌症有关,但尚未有任何具体的研究来检验NLRP3多态性与癌症(CC)之间的关系。因此,本研究旨在研究NLRP3基因多态性对中国南方人群HPV感染和宫颈癌症的影响。方法:采用多重PCR和下一代测序方法评估404例宫颈病变患者的NLRP3 rs10754558和rs10733113多态性,其中227例诊断为CC,177例诊断为宫颈上皮内瘤变(CIN),419名健康女性对照进行比较。然后分析这些患者的rs10754558和rs10733113基因型和等位基因与CC和CIN之间的相关性。结果:NLRP3 rs10754558和rs10733113与人乳头瘤病毒(HPV)感染状况无相关性。相对于健康对照组,NLRP3 rs10754558 GG基因型,CG + GG基因型和G等位基因频率在宫颈病变(CC和CIN)患者中显著增加(OR = 1.815,P = 0.013;或 = 1.383,P = 0.026;或 = 1.284,P = 0.014),而rs10733113没有观察到这种差异。年龄在45岁以上的rs10754558GG基因型患者的宫颈病变风险较高(OR = 1.848,P = 0.040)。此外,与CC基因型或C等位基因的患者相比,rs10754558 GG基因型或G等位基因患者患CC的风险升高(or = 1.830,P = 0.029;或 = 1.281,P = rs10733113基因型或等位基因与CC风险无显著相关性(P > rs10754558和rs10733113基因型与CC患者临床病理特征无相关性(P > 与健康对照组相比,CC患者血清NLRP3、IL-1β和IL-18水平显著升高(P 结论:NLRP3基因rs10754558多态性可能导致CC风险升高,尽管它与HPV感染和CC进展没有显著相关性。
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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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