Impact of IL31RA Genetic Variants and Expression on Metastatic Progression in Oral Cavity Squamous Cell Carcinoma.

IF 4.6 4区 医学 Q3 ONCOLOGY
Oncology Research Pub Date : 2026-08-13 eCollection Date: 2026-01-01 DOI:10.32604/or.2026.080527
Hsueh-Ju Lu, Chiao-Wen Lin, Chun-Yi Chuang, Chun-Wen Su, Shun-Fa Yang
{"title":"Impact of <i>IL31RA</i> Genetic Variants and Expression on Metastatic Progression in Oral Cavity Squamous Cell Carcinoma.","authors":"Hsueh-Ju Lu, Chiao-Wen Lin, Chun-Yi Chuang, Chun-Wen Su, Shun-Fa Yang","doi":"10.32604/or.2026.080527","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background:</b> Interleukin-31 receptor alpha (IL31RA) has been implicated in cancer progression and tumor cell migration, but its genetic associations across cancers remain unclear. This study aimed to examine <i>IL31RA</i> polymorphisms in relation to lymph node involvement in oral cavity squamous cell carcinoma (OCSCC). <b>Methods:</b> In this case-control study, 2845 participants were enrolled, including 1352 patients with OCSCC and 1493 cancer-free controls. Associations between <i>IL31RA</i> SNPs and OCSCC susceptibility and clinicopathological characteristics were evaluated. Functional analyses, including cell migration assays, together with bioinformatic database analyses, were performed to investigate the biological significance of IL31RA and genotype-expression correlations. Logistic regression and other appropriate statistical methods were used to assess these associations. <b>Results:</b> <i>IL31RA</i> polymorphisms did not significantly influence OCSCC development. However, subsite-specific analysis revealed that gingival cancer patients with minor alleles at rs6876491 and rs10055201 had significantly higher lymph node involvement rates than wild-type carriers. <i>IL31RA</i> rs6876491 was also an independent predictor of lymph node involvement in gingival cancer after adjusting for clinical characteristics, with adjusted odds ratios of 2.172 (95% Confidence Interval: 1.095-4.310). Bioinformatic databases also showed that minor genotypes correlated with increased IL31RA expression. Patients with higher IL31RA expression tended to have poorer survival in head and neck squamous cell carcinoma (HNSCC) based on TCGA public database analyses (<i>p</i> = 0.053). Moreover, functional studies confirmed that IL31RA overexpression enhanced cellular migration (<i>p</i> < 0.05), while knockdown suppressed migratory capacity (<i>p</i> < 0.05). <b>Conclusions:</b> <i>IL31RA</i> polymorphisms may be associated with an increased propensity for lymph node involvement, particularly in gingival cancer, suggesting that IL31RA may have potential clinical relevance in OCSCC progression.</p>","PeriodicalId":19537,"journal":{"name":"Oncology Research","volume":"34 9","pages":"17"},"PeriodicalIF":4.6000,"publicationDate":"2026-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13494500/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oncology Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.32604/or.2026.080527","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Interleukin-31 receptor alpha (IL31RA) has been implicated in cancer progression and tumor cell migration, but its genetic associations across cancers remain unclear. This study aimed to examine IL31RA polymorphisms in relation to lymph node involvement in oral cavity squamous cell carcinoma (OCSCC). Methods: In this case-control study, 2845 participants were enrolled, including 1352 patients with OCSCC and 1493 cancer-free controls. Associations between IL31RA SNPs and OCSCC susceptibility and clinicopathological characteristics were evaluated. Functional analyses, including cell migration assays, together with bioinformatic database analyses, were performed to investigate the biological significance of IL31RA and genotype-expression correlations. Logistic regression and other appropriate statistical methods were used to assess these associations. Results: IL31RA polymorphisms did not significantly influence OCSCC development. However, subsite-specific analysis revealed that gingival cancer patients with minor alleles at rs6876491 and rs10055201 had significantly higher lymph node involvement rates than wild-type carriers. IL31RA rs6876491 was also an independent predictor of lymph node involvement in gingival cancer after adjusting for clinical characteristics, with adjusted odds ratios of 2.172 (95% Confidence Interval: 1.095-4.310). Bioinformatic databases also showed that minor genotypes correlated with increased IL31RA expression. Patients with higher IL31RA expression tended to have poorer survival in head and neck squamous cell carcinoma (HNSCC) based on TCGA public database analyses (p = 0.053). Moreover, functional studies confirmed that IL31RA overexpression enhanced cellular migration (p < 0.05), while knockdown suppressed migratory capacity (p < 0.05). Conclusions: IL31RA polymorphisms may be associated with an increased propensity for lymph node involvement, particularly in gingival cancer, suggesting that IL31RA may have potential clinical relevance in OCSCC progression.

IL31RA基因变异及其表达对口腔鳞状细胞癌转移进展的影响
背景:白细胞介素-31受体α (IL31RA)与癌症进展和肿瘤细胞迁移有关,但其在癌症中的遗传关联尚不清楚。本研究旨在探讨IL31RA多态性与口腔鳞状细胞癌(OCSCC)淋巴结累及的关系。方法:在本病例对照研究中,纳入2845名参与者,其中包括1352例OCSCC患者和1493例无癌对照。评估IL31RA snp与OCSCC易感性和临床病理特征之间的关系。通过功能分析,包括细胞迁移分析,以及生物信息学数据库分析,研究IL31RA的生物学意义和基因型表达相关性。使用逻辑回归和其他适当的统计方法来评估这些关联。结果:IL31RA多态性对OCSCC的发展无显著影响。然而,亚位特异性分析显示,携带rs6876491和rs10055201等位基因的牙龈癌患者的淋巴结累及率明显高于野生型携带者。在调整临床特征后,IL31RA rs6876491也是牙龈癌淋巴结累及的独立预测因子,调整后的优势比为2.172(95%可信区间:1.095-4.310)。生物信息学数据库也显示,少量基因型与IL31RA表达增加相关。TCGA公共数据库分析显示,IL31RA高表达的头颈部鳞状细胞癌(HNSCC)患者生存率较低(p = 0.053)。此外,功能研究证实,IL31RA过表达增强了细胞迁移(p < 0.05),而敲低抑制了细胞迁移能力(p < 0.05)。结论:IL31RA多态性可能与淋巴结累及倾向增加有关,特别是在牙龈癌中,这表明IL31RA可能与OCSCC进展具有潜在的临床相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Oncology Research
Oncology Research 医学-肿瘤学
CiteScore
4.40
自引率
0.00%
发文量
56
审稿时长
3 months
期刊介绍: Oncology Research Featuring Preclinical and Clincal Cancer Therapeutics publishes research of the highest quality that contributes to an understanding of cancer in areas of molecular biology, cell biology, biochemistry, biophysics, genetics, biology, endocrinology, and immunology, as well as studies on the mechanism of action of carcinogens and therapeutic agents, reports dealing with cancer prevention and epidemiology, and clinical trials delineating effective new therapeutic regimens.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书