| Autor: |
Mao, Zhenguang, Gao, Fang, Sun, Tuo, Xiao, Yi, Wu, Jiajin, Xiao, Yanping, Chu, Haiyan, Wu, Dongmei, Du, Mulong, Zheng, Rui, Zhang, Zhengdong |
| Zdroj: |
Environmental Toxicology; Dec2024, Vol. 39 Issue 12, p5357-5370, 14p |
| Abstrakt: |
Cigarette smoking causes multiple cancers by directly influencing mutation burden of driver mutations. However, the mechanism between somatic mutation caused by cigarette smoking and bladder tumorigenesis remains elusive. Smoking‐related mutation profile of bladder cancer was characterized by The Cancer Genome Atlas cohort. Integraticve OncoGenomics database was utilized to detect the smoking‐related driver genes, and its biological mechanism predictions were interpreted based on bulk transcriptome and single‐cell transcriptome, as well as cell experiments. Cigarette smoking was associated with an increased tumor mutational burden under 65 years old (p = 0.031), and generated specific mutational signatures in smokers. RB1 was identified as a differentially mutated driver gene between smokers and nonsmokers, and the mutation rate of RB1 increased twofold after smoking (p = 0.008). RB1 mutations and the 4‐aminobiphenyl interference could significantly decrease the RB1 expression level and thus promote the proliferation, invasion, and migration ability of bladder cancer cells. Enrichment analysis and real‐time quantitative PCR (RT‐qPCR) data showed that RB1 mutations inhibited cytochrome P450 pathway by reducing expression levels of UGT1A6 and AKR1C2. In addition, we also observed that the component of immunological cells was regulated by RB1 mutations through the stronger cell‐to‐cell interactions between epithelial scissor+ cells and immune cells in smokers. This study highlighted that RB1 mutations could drive smoking‐related bladder tumorigenesis through inhibiting cytochrome P450 pathway and regulating tumor immune microenvironment. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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