Chen Min, Chen Qian, Xiao Xin-Yu, Feng Si-Jia, Wang Xiao-Ying, Tang Tai-Chun, Zheng Hui
Department of Colorectal Diseases, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
The Third Hospital/Acupuncture and Tuina School, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Front Pharmacol. 2022 Dec 23;13:1079953. doi: 10.3389/fphar.2022.1079953. eCollection 2022.
Previous studies suggested that anti-TNF drugs might be repurposed as a preventive treatment for colorectal cancer. We aimed to examine whether genetically proxied inhibition of tumor necrosis factor receptor 1 (TNFR1) reduces the absolute risk of colorectal cancer through mendelian randomization (MR) analysis. We obtained 28 single nucleotide polymorphisms (SNPs) that were located within a ±15 kilobase window of the TNFRSF1A-the gene that encodes the TNFR1 protein, and we used genetic data from three GWAS studies of circulating levels of TNFR1, C-reactive protein (CRP), and white blood counts (WBC) to screen SNPs that proxied the inhibition of TNFR1. Positive control analyses were then performed by using another three GWAS data from the ulcerative colitis cohort ( = 45,975), Crohn's disease cohort ( = 40,266), and multiple sclerosis cohort ( = 115,803) to confirm the effect of the included SNPs. A two-sample mendelian randomization analysis was performed to examine the association between TNFR1 inhibition and the absolute risk reduction (ARR) of colorectal cancer. We finally included seven SNPs to proxy the anti-TNF effect, and these SNPs caused lower levels of TNFR1, CRP, and white blood counts. In positive control analyses, the included SNPs caused lower odds ratio of ulcerative colitis and Crohn's disease but a higher odds ratio of multiple sclerosis, consistent with drug mechanistic actions and previous trial evidence. By using the inverse-variance weighted analyses to combine the effects of the seven SNPs, we found that the anti-TNF effect was associated with a 0.988 (95%CI 0.985-0.991) mg/L decrease in CRP levels and a reduction in the risk of colorectal cancer (absolute risk reduction -2.1%, 95%CI -3.8% to -0.4%, = 0.01). Our study confirmed that anti-TNF drugs were associated with a risk reduction in colorectal cancer. Physicians could consider using anti-TNF drugs for the prevention of colorectal cancer, especially in patients with high risks of developing cancer.
以往的研究表明,抗TNF药物可能被重新用作结直肠癌的预防性治疗药物。我们旨在通过孟德尔随机化(MR)分析,研究基因代理的肿瘤坏死因子受体1(TNFR1)抑制是否能降低结直肠癌的绝对风险。我们获得了28个单核苷酸多态性(SNP),这些SNP位于编码TNFR1蛋白的基因TNFRSF1A的±15千碱基窗口内,并使用来自三项GWAS研究的遗传数据,这些研究涉及TNFR1、C反应蛋白(CRP)和白细胞计数(WBC)的循环水平,以筛选代理TNFR1抑制的SNP。然后,通过使用来自溃疡性结肠炎队列(n = 45975)、克罗恩病队列(n = 40266)和多发性硬化症队列(n = 115803)的另外三项GWAS数据进行阳性对照分析,以确认所纳入SNP的效应。进行了两样本孟德尔随机化分析,以研究TNFR1抑制与结直肠癌绝对风险降低(ARR)之间的关联。我们最终纳入了7个SNP来代理抗TNF效应,这些SNP导致TNFR1、CRP和白细胞计数水平降低。在阳性对照分析中,所纳入的SNP导致溃疡性结肠炎和克罗恩病的比值比降低,但多发性硬化症的比值比升高,这与药物作用机制和先前的试验证据一致。通过使用逆方差加权分析来合并7个SNP的效应,我们发现抗TNF效应与CRP水平降低0.988(95%CI 0.985 - 0.991)mg/L以及结直肠癌风险降低相关(绝对风险降低 -2.1%,95%CI -3.8%至 -0.4%,P = 0.01)。我们的研究证实,抗TNF药物与结直肠癌风险降低相关。医生可以考虑使用抗TNF药物来预防结直肠癌,尤其是在癌症发生风险较高的患者中。