Yang BoWen, Zeng XiaoYu, Wang HanYu, Feng JiuHuan, Hou ShuFang
Oncology, Dongguan Hospital of Guangzhou University of Chinese Medicine, Dongguan, Guangdong, China.
Graduate School of Guangzhou, University of Traditional Chinese Medicine, Guangzhou, China.
Am J Mens Health. 2025 Jan-Feb;19(1):15579883241311229. doi: 10.1177/15579883241311229.
Many observational epidemiological studies have reported an association between matrix metalloproteinases (MMPs) and urologic cancers. However, the causal relationship between these two phenotypes remains uncertain. This study aims to examine the bidirectional causal relationship between serum MMPs and three urologic cancers: kidney, prostate, and bladder cancer. Using data from large-scale genome-wide association studies (GWAS), we employed two-sample Mendelian randomization (MR) methods to assess the causal relationship between serum MMPs and urologic cancers. We performed inverse variance-weighted MR as the primary method for calculating the overall effects of multiple instruments, while implementing additional MR methods and sensitivity analyses. Odds ratios (ORs) were employed to evaluate the causal relationship between serum MMPs and urologic cancers risk. Our findings indicated a causal relationship between serum MMP-3 levels and prostate cancer risk (OR = 1.07, 95% confidence interval [CI] = [1.02, 1.11], = .003). There was a possible causal relationship between serum MMP-1 and prostate cancer (OR = 0.95, 95% CI = [0.92, 0.99], = .02). Serum MMP-1 may also increase the risk of bladder cancer (OR = 1.24, 95% CI = [1.04, 1.49], = .016). We did not find significant associations of the remaining MMPs with prostate, bladder, and kidney cancer. In reverse MR, no significant results were observed supporting the effect of urologic cancers on MMPs ( > .05). Our study provides evidence of a potential causal relationship between serum MMPs and both prostate cancer and bladder cancer. However, large-scale studies are necessary to confirm and reveal the underlying mechanisms of this association.
许多观察性流行病学研究报告了基质金属蛋白酶(MMPs)与泌尿系统癌症之间的关联。然而,这两种表型之间的因果关系仍不确定。本研究旨在探讨血清MMPs与三种泌尿系统癌症(肾癌、前列腺癌和膀胱癌)之间的双向因果关系。利用大规模全基因组关联研究(GWAS)的数据,我们采用双样本孟德尔随机化(MR)方法来评估血清MMPs与泌尿系统癌症之间的因果关系。我们将逆方差加权MR作为计算多种工具总体效应的主要方法,同时实施额外的MR方法和敏感性分析。采用优势比(OR)来评估血清MMPs与泌尿系统癌症风险之间的因果关系。我们的研究结果表明血清MMP - 3水平与前列腺癌风险之间存在因果关系(OR = 1.07,95%置信区间[CI] = [1.02, 1.11],P = .003)。血清MMP - 1与前列腺癌之间可能存在因果关系(OR = 0.95,95% CI = [0.92, 0.99],P = .02)。血清MMP - 1也可能增加膀胱癌的风险(OR = 1.24,95% CI = [1.04, 1.49],P = .016)。我们未发现其余MMPs与前列腺癌、膀胱癌和肾癌之间存在显著关联。在反向MR中,未观察到支持泌尿系统癌症对MMPs有影响的显著结果(P > .05)。我们的研究提供了血清MMPs与前列腺癌和膀胱癌之间潜在因果关系的证据。然而,需要大规模研究来证实并揭示这种关联的潜在机制。