Shu Xiang, Sun Jing, Zhang Meng, Li Xinxuan, Yang Nan, Sun Xiaohui, Wang Xinjun, Guo Xingyi, Buas Matthew, Watt Gordon, Li Xue
Memorial Sloan Kettering Cancer Center.
Zhejiang University School of Medicine.
Res Sq. 2025 May 7:rs.3.rs-6491161. doi: 10.21203/rs.3.rs-6491161/v1.
Although prior studies have reported a link between autoimmunity and carcinogenesis, the roles of genetic factors and potential mediators involved in this process remain elusive. We constructed disease-specific and combined polygenic risk scores (PRSs) for 6 common autoimmune diseases (AIDs) (systemic lupus erythematosus [SLE], rheumatoid arthritis, multiple sclerosis, Crohn's disease, ulcerative colitis [UC], and type 1 diabetes mellitus [T1D]) in the UK Biobank cohort. Compared to those without AID, AID patients at baseline had increased risks of overall cancer, hematological, digestive, and urinary cancer. The combined AID-PRS was significantly associated with increased risks of hematological cancer (HR [95% CI] per SD increase: 1.06 [1.03-1.09]) and non-Hodgkin's lymphoma (HR [95% CI] per SD increase: 1.10 [1.05-1.14]). For individual AID-PRSs, we identified 21 significant associations between 5 PRSs and 11 types of cancer in the overall population, along with 15 additional associations in the sex-stratified analysis. For example, SLE-, UC-, and T1D-PRS showed complex cross-cancer effects on risks of up to 6 cancer types. These associations were generally independent of immunosuppressant drug use. Differential associations of SLE-PRS with prostate cancer risk were found by prostate cancer PRS status ( <0.05). Several peripheral biomarkers, including red or white blood cell counts, platelet counts, and CRP partly mediated the PRS associations (up to 16.96%). Our study provides important insights into the role of autoimmune diseases in carcinogenesis, which also highlights opportunities for target cancer screening and prevention in potentially vulnerable populations.
尽管先前的研究报道了自身免疫与致癌作用之间的联系,但参与这一过程的遗传因素和潜在介质的作用仍不明确。我们在英国生物银行队列中构建了6种常见自身免疫性疾病(AIDs)(系统性红斑狼疮[SLE]、类风湿性关节炎、多发性硬化症、克罗恩病、溃疡性结肠炎[UC]和1型糖尿病[T1D])的疾病特异性和综合多基因风险评分(PRSs)。与无AID的人相比,基线时的AID患者患总体癌症、血液系统癌症、消化系统癌症和泌尿系统癌症的风险增加。综合AID-PRS与血液系统癌症风险增加显著相关(每标准差增加的HR[95%CI]:1.06[1.03-1.09])和非霍奇金淋巴瘤(每标准差增加的HR[95%CI]:1.10[1.05-1.14])。对于个体AID-PRSs,我们在总体人群中确定了5个PRS与11种癌症类型之间的21个显著关联,以及在按性别分层分析中的另外15个关联。例如,SLE-、UC-和T1D-PRS对多达6种癌症类型的风险显示出复杂的跨癌症效应。这些关联通常独立于免疫抑制药物的使用。通过前列腺癌PRS状态发现SLE-PRS与前列腺癌风险的差异关联(<0.05)。包括红细胞或白细胞计数、血小板计数和CRP在内的几种外周生物标志物部分介导了PRS关联(高达16.96%)。我们的研究为自身免疫性疾病在致癌作用中的作用提供了重要见解,这也凸显了在潜在易感人群中进行靶向癌症筛查和预防的机会。