Xing Wenjing, Xiao Yun, Lu Xinliang, Zhu Hongyan, He Xiangchuan, Huang Wei, Lopez Elsa S, Wong Jerry, Ju Huanyu, Tian Linlu, Zhang Fengmin, Xu Hongwei, Wang Sheng Dian, Li Xia, Karin Michael, Ren Huan
Department of Immunology, Harbin Medical University, Harbin 150081, China.
Immunity & Infection Key laboratory of Heilongjiang Province, Harbin 150081, China.
Cell Death Differ. 2017 May;24(5):929-943. doi: 10.1038/cdd.2017.50. Epub 2017 Apr 7.
Inflammation is frequently associated with initiation, progression, and metastasis of colorectal cancer (CRC). Here, we unveil a CRC-specific metastatic programme that is triggered via the transcriptional repressor, GFI1. Using data from a large cohort of clinical samples including inflammatory bowel disease and CRC, and a cellular model of CRC progression mediated by cross-talk between the cancer cell and the inflammatory microenvironment, we identified GFI1 as a gating regulator responsible for a constitutively activated signalling circuit that renders CRC cells competent for metastatic spread. Further analysis of mouse models with metastatic CRC and human clinical specimens reinforced the influence of GFI1 downregulation in promoting CRC metastatic spread. The novel role of GFI1 is uncovered for the first time in a human solid tumour such as CRC. Our results imply that GFI1 is a potential therapeutic target for interfering with inflammation-induced CRC progression and spread.
炎症常常与结直肠癌(CRC)的起始、进展和转移相关。在此,我们揭示了一种由转录抑制因子GFI1触发的CRC特异性转移程序。利用来自包括炎症性肠病和CRC在内的大量临床样本队列的数据,以及由癌细胞与炎症微环境之间的相互作用介导的CRC进展细胞模型,我们确定GFI1是一种门控调节因子,负责一个组成性激活的信号通路,该通路使CRC细胞具备转移扩散的能力。对转移性CRC小鼠模型和人类临床标本的进一步分析强化了GFI1下调在促进CRC转移扩散中的作用。GFI1的这一新作用首次在诸如CRC这样的人类实体瘤中被发现。我们的结果表明,GFI1是干扰炎症诱导的CRC进展和扩散的潜在治疗靶点。