Bacterial infection promotes tumorigenesis of colorectal cancer via regulating CDC42 acetylation

作者：Danni Wang, Jinjing Ni, Jianhui Li, Yaqi Gao, Fangjing Ni, Zhenzhen Zhang, Jing‐Yuan Fang, Jie Lu, Yufeng Yao · 发表于：PLoS Pathogens · 年份：2023 · DOI：10.1371/journal.ppat.1011189 · 被引用次数：14 · 研究领域：Sirtuins and Resveratrol in Medicine、Autophagy in Disease and Therapy、Cancer Research and Treatments

Increasing evidence highlights the role of bacteria in promoting tumorigenesis. The underlying mechanisms may be diverse and remain poorly understood. Here, we report that Salmonella infection leads to extensive de/acetylation changes in host cell proteins. The acetylation of mammalian cell division cycle 42 (CDC42), a member of the Rho family of GTPases involved in many crucial signaling pathways in cancer cells, is drastically reduced after bacterial infection. CDC42 is deacetylated by SIRT2 and acetylated by p300/CBP. Non-acetylated CDC42 at lysine 153 shows an impaired binding of its downstream effector PAK4 and an attenuated phosphorylation of p38 and JNK, consequently reduces cell apoptosis. The reduction in K153 acetylation also enhances the migration and invasion ability of colon cancer cells. The low level of K153 acetylation in patients with colorectal cancer (CRC) predicts a poor prognosis. Taken together, our findings suggest a new mechanism of bacterial infection-induced promotion of colorectal tumorigenesis by modulation of the CDC42-PAK axis through manipulation of CDC42 acetylation.