APOBEC-mediated mutagenesis is a favorable predictor of prognosis and immunotherapy for bladder cancer patients: evidence from pan-cancer analysis and multiple databases

阿波贝克 突变 生物 癌症 癌症研究 免疫疗法 计算生物学 转录组 突变 遗传学 基因组 基因 基因表达
作者
Run Shi,Xin Wang,Yang Wu,Bin Xu,Tianyu Zhao,Christian Trapp,Xuanbin Wang,Kristian Unger,Cheng Zhou,Shun Lü,Alexander Büchner,Gerald Bastian Schulz,Fengjun Cao,C. Belka,Chuan Su,Minglun Li,Yongqian Shu
出处
期刊:Theranostics [Ivyspring International Publisher]
卷期号:12 (9): 4181-4199 被引量:19
标识
DOI:10.7150/thno.73235
摘要

Background: The APOBEC (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like) family-mediated mutagenesis is widespread in human cancers. However, our knowledge of the biological feature and clinical relevance of APOBECs and APOBEC mutagenesis in cancers remains limited. Methods: In this study, with a series of bioinformatic and statistical approaches, we performed a comprehensive analysis of multiple levels of data, including whole-exome sequencing (WES) and targeted next-generation sequencing (NGS), transcriptome (bulk RNA-seq and single-cell RNA-seq), immune signatures and immune checkpoint blockade (ICB) potential, patient survival and drug sensitivity, to reveal the distribution characteristics and clinical significance of APOBECs and APOBEC mutagenesis in pan-cancer especially bladder cancer (BLCA). Results: APOBEC mutagenesis dominates in the mutational patterns of BLCA. A higher enrichment score of APOBEC mutagenesis correlates with favorable prognosis, immune activation and potential ICB response in BLCA patients. APOBEC3A and 3B play a significant role in the malignant progression and cell differentiation within the tumor microenvironment. Furthermore, using machine learning approaches, a prognostic APOBEC mutagenesis-related model was established and validated in different BLCA cohorts. Conclusions: Our study illustrates the characterization of APOBECs and APOBEC mutagenesis in multiple cancer types and highlights its potential value as a promising biomarker for prognosis and immunotherapy in BLCA.
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