Yu Xiaopeng, Tang Yutian, Niu Junjie, Hu Jinyang
Hunan Provincial Hospital of Integrated Traditional Chinese and Western Medicine & Hunan University of Chinese Medicine, Changsha, Hunan Province, PR China.
School of Integrated Chinese and Western Medicine, Hunan University of Chinese Medicine, Changsha, Hunan, PR China.
Cancer Gene Ther. 2025 Jul 18. doi: 10.1038/s41417-025-00917-5.
This study aimed to investigate the molecular mechanisms underlying ulcerative colitis (UC)-associated colorectal cancer (CRC) development and identify potential therapeutic targets through integrated multi-omics analysis. Mendelian randomization (MR) analysis, combined with bioinformatics approaches including differential gene expression analysis, protein-protein interaction network construction, gene set enrichment analysis, and single-cell RNA sequencing, was employed. Data were obtained from GEO, TCGA, and genome-wide association study (GWAS) databases. Drug prediction and molecular docking were performed using DSigDB and AutoDockTools. A total of 48 shared genes were identified between UC and CRC, with MMP1 emerging as a significant protective factor (OR = 0.766; 95% CI = 0.593-0.989, P = 0.041). MMP1 demonstrated strong diagnostic potential (AUC = 0.927, 95% CI = 0.895-0.959) and was functionally associated with immune regulation and metabolic pathways. Single-cell analysis revealed predominant MMP1 expression in fibroblasts and immune cells, while immune infiltration analysis showed significant correlations with CD8⁺ T cells and NK cells. Mediation MR analysis indicated that 63.33% of MMP1's protective effect was mediated through naive-mature B cells. Drug prediction identified ilomastat as a potential MMP1 inhibitor with strong binding affinity (binding energy = -7.17 kcal/mol). These findings provide evidence for MMP1's protective role in UC-associated CRC through immune microenvironment modulation, highlighting its potential as a diagnostic biomarker and therapeutic target. The identification of ilomastat as a potential MMP1 inhibitor offers new avenues for targeted therapy in inflammation-associated cancers.
本研究旨在通过综合多组学分析,探究溃疡性结肠炎(UC)相关结直肠癌(CRC)发生发展的分子机制,并确定潜在的治疗靶点。采用了孟德尔随机化(MR)分析,并结合包括差异基因表达分析、蛋白质-蛋白质相互作用网络构建、基因集富集分析和单细胞RNA测序在内的生物信息学方法。数据来源于GEO、TCGA和全基因组关联研究(GWAS)数据库。使用DSigDB和AutoDockTools进行药物预测和分子对接。在UC和CRC之间共鉴定出48个共享基因,其中基质金属蛋白酶1(MMP1)成为一个显著的保护因子(比值比=0.766;95%置信区间=0.593-0.989,P=0.041)。MMP1具有很强的诊断潜力(曲线下面积=0.927,95%置信区间=0.895-0.959),并且在功能上与免疫调节和代谢途径相关。单细胞分析显示成纤维细胞和免疫细胞中MMP1表达占主导,而免疫浸润分析表明其与CD8⁺T细胞和自然杀伤细胞有显著相关性。中介MR分析表明,MMP1保护作用的63.33%是通过幼稚-成熟B细胞介导的。药物预测确定抑肽酶为一种具有强结合亲和力的潜在MMP1抑制剂(结合能=-7.17千卡/摩尔)。这些发现为MMP1通过调节免疫微环境在UC相关CRC中的保护作用提供了证据,突出了其作为诊断生物标志物和治疗靶点的潜力。抑肽酶作为潜在MMP1抑制剂的鉴定为炎症相关癌症的靶向治疗提供了新途径。