Integrative machine learning algorithms for developing a consensus RNA modification-based signature for guiding clinical decision-making in bladder cancer

Author:

Jia Shijun1,Zhai Linhan12,Wu Feng1,Lv Wenzhi3,Min Xiangde2,Zhang Shuang1,Li Feng1

Affiliation:

1. Department of Radiology, Xiangyang Central Hospital , Affiliated Hospital of Hubei University of Arts and Science , Xiangyang , Hubei , China

2. Department of Radiology, Tongji Hospital, Tongji Medical College , Huazhong University of Science and Technology , Wuhan , Hubei , China

3. Department of Artificial Intelligence , Julei Technology Company , Wuhan , Hubei , China

Abstract

Abstract Objectives Dysregulation of RNA modifications has emerged as a contributor to cancer, but the clinical implication of RNA modification-related genes remains largely unclear. The study focused on well-studied RNA modification modalities (m6A, m1A, m5C and m7G) in bladder cancer, and proposed a machine learning-based integrative approach for establishing a consensus RNA modification-based signature. Methods Multiple publicly available bladder cancer cohorts were enrolled. A novel RNA modification-based classification was proposed via consensus clustering analysis. RNA modification-related genes were subsequently selected through WGCNA. A machine learning-based integrative framework was implemented for constructing a consensus RNA modification-based signature. Results Most RNA modifiers were dysregulated in bladder tumours at the multi-omics levels. Two RNA modification clusters were identified, with diverse prognostic outcomes. A consensus RNA modification-based signature was established, which displayed stable and powerful efficacy in prognosis estimation. Notably, the signature was superior to conventional clinical indicators. High-risk tumours presented the activation of tumourigenic pathways, with the activation of metabolism pathways in low-risk tumours. The low-risk group was more sensitive to immune-checkpoint blockade, with the higher sensitivity of the high-risk group to cisplatin and paclitaxel. Genes in the signature: AKR1B1, ANXA1, CCNL2, OAS1, PTPN6, SPINK1 and TNFRSF14 were specially expressed in distinct T lymphocytes of bladder tumours at the single-cell level, potentially participating in T cell-mediated antitumour immunity. They were transcriptionally and post-transcriptionally modulated, and might become potentially actionable therapeutic targets. Conclusions Altogether, the consensus RNA modification-based signature may act as a reliable and hopeful tool for improving clinical decision-making for individual bladder cancer patients.

Funder

The key program of scientific research foundation in the field of health and medicine of Xiangyang

The general program of scientific research foundation of Xiangyang Central Hospital

The key program of scientific research foundation of Hubei

Publisher

Walter de Gruyter GmbH

Subject

Oncology

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