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.
- Shi, R.
- Wang, X.
- Wu, Y.
- Xu, B.
- Zhao, T.
- Trapp, C.
- Wang, X.
- Unger, K.
- Zhou, C.
- Lu, S.
- Buchner, A.
- Schulz, G. B.
- Cao, F.
- Belka, C.
- Su, C.
- Li, M.
- Shu, Y.
Keywords
- Cytidine Deaminase/genetics
- Humans
- Immunotherapy
- Mutagenesis
- Proteins
- Tumor Microenvironment
- *Urinary Bladder Neoplasms/genetics/pathology/therapy
- APOBEC mutagenesis
- Pan-cancer analysis
- Prognosis