Artificial intelligence‐driven consensus gene signatures for improving bladder cancer clinical outcomes identified by multi‐center integration analysis

肿瘤科 膀胱癌 基因签名 阶段(地层学) 精密医学 内科学 医学 癌症 生物信息学 机器学习 基因 生物 计算机科学 病理 基因表达 古生物学 生物化学
作者
Hui Xu,Zaoqu Liu,Siyuan Weng,Qin Dang,Xiaoyong Ge,Yuyuan Zhang,Yuqing Ren,Zhe Xing,Shuang Chen,Yifang Zhou,Jianzhuang Ren,Xinwei Han
出处
期刊:Molecular Oncology [Elsevier BV]
卷期号:16 (22): 4023-4042 被引量:16
标识
DOI:10.1002/1878-0261.13313
摘要

To accurately predict the prognosis and further improve the clinical outcomes of bladder cancer (BLCA), we leveraged large-scale data to develop and validate a robust signature consisting of small gene sets. Ten machine-learning algorithms were enrolled and subsequently transformed into 76 combinations, which were further performed on eight independent cohorts (n = 1218). We ultimately determined a consensus artificial intelligence-derived gene signature (AIGS) with the best performance among 76 model types. In this model, patients with high AIGS showed a higher risk of mortality, recurrence, and disease progression. AIGS is not only independent of traditional clinical traits [(e.g., American Joint Committee on Cancer (AJCC) stage)] and molecular features (e.g., TP53 mutation) but also demonstrated superior performance to these variables. Comparisons with 58 published signatures also indicated that AIGS possessed the best performance. Additionally, the combination of AIGS and AJCC stage could achieve better performance. Patients with low AIGS scores were sensitive to immunotherapy, whereas patients with high AIGS scores might benefit from seven potential therapeutics: BRD-K45681478, 1S,3R-RSL-3, RITA, U-0126, temsirolimus, MRS-1220, and LY2784544. Additionally, some mutations (TP53 and RB1), copy number variations (7p11.2), and a methylation-driven target were characterized by AIGS-related multi-omics alterations. Overall, AIGS provides an attractive platform to optimize decision-making and surveillance protocol for individual BLCA patients.

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