Artificial intelligence-driven consensus gene signatures for improving bladder cancer clinical outcomes identified by multi-center integration analysis.
Hui XuZaoqu LiuSiyuan WengQin DangXiaoyong GeYuyuan ZhangYuqing RenZhe XingShuang ChenYifang ZhouJianzhuang RenXin-Wei HanPublished in: Molecular oncology (2022)
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.
Keyphrases
- artificial intelligence
- copy number
- genome wide
- machine learning
- big data
- mitochondrial dna
- deep learning
- dna methylation
- end stage renal disease
- ejection fraction
- decision making
- randomized controlled trial
- chronic kidney disease
- risk factors
- high throughput
- public health
- cardiovascular disease
- type diabetes
- risk assessment
- clinical practice
- squamous cell carcinoma
- climate change
- systematic review
- papillary thyroid
- muscle invasive bladder cancer