Wang Meng, Liu Kailin, Bao Wu, Hang Bingqing, Chen Xianjiong, Zhu Xinyi, Li Guifang, Liu Lihong, Xiang Haoyi, Hu Hai, Lu Yanhui, Song Zhangfa, Chen Jiaxin, Wang Yuhao
Zhejiang Provincial Key Laboratory of Pancreatic Disease of The First Affiliated Hospital, Institute of Translational Medicine, Zhejiang University School of Medicine, Hangzhou 310029, Zhejiang, China.
Department of Radiation Oncology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, Zhejiang, China.
Dev Cell. 2025 Apr 7;60(7):1008-1017.e7. doi: 10.1016/j.devcel.2024.12.013. Epub 2025 Jan 3.
The intestinal microbiota is a key environmental factor in the development of colorectal cancer (CRC). Here, we report that, in the context of mild colonic inflammation, the microbiota protects against colorectal tumorigenesis in mice. This protection is achieved by microbial suppression of the long non-coding RNA (lncRNA) Snhg9. Snhg9 promotes tumor growth through inhibition of the tumor suppressor p53. Snhg9 suppresses p53 activity by dissociating the p53 deacetylase sirtuin 1 (SIRT1) from the cell cycle and apoptosis regulator 2 (CCAR2). Consequently, the depletion of the microbiota by antibiotics causes upregulation of Snhg9 and accelerates CRC progression. Moreover, Snhg9 is functionally conserved. Human SNHG9 promotes tumor growth via the same mechanism as mouse Snhg9, despite their low sequence similarity.
肠道微生物群是结直肠癌(CRC)发生发展的关键环境因素。在此,我们报告,在轻度结肠炎症的背景下,微生物群可保护小鼠免受结直肠癌的发生。这种保护是通过微生物对长链非编码RNA(lncRNA)Snhg9的抑制来实现的。Snhg9通过抑制肿瘤抑制因子p53促进肿瘤生长。Snhg9通过使p53去乙酰化酶沉默调节蛋白1(SIRT1)与细胞周期和凋亡调节因子2(CCAR2)解离来抑制p53活性。因此,抗生素导致的微生物群耗竭会引起Snhg9上调并加速结直肠癌进展。此外,Snhg9在功能上是保守的。尽管人类SNHG9与小鼠Snhg9的序列相似性较低,但它们通过相同的机制促进肿瘤生长。