Interleukin-11-expressing fibroblasts have a unique gene signature correlated with poor prognosis of colorectal cancer

表达白细胞介素-11的成纤维细胞具有独特的基因特征,该特征与结直肠癌预后不良相关。

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作者:Takashi Nishina ,Yutaka Deguchi ,Daisuke Ohshima ,Wakami Takeda ,Masato Ohtsuka ,Shigeyuki Shichino ,Satoshi Ueha ,Soh Yamazaki ,Mika Kawauchi ,Eri Nakamura ,Chiharu Nishiyama ,Yuko Kojima ,Satomi Adachi-Akahane ,Mizuho Hasegawa ,Mizuho Nakayama ,Masanobu Oshima ,Hideo Yagita ,Kazutoshi Shibuya ,Tetuo Mikami ,Naohiro Inohara ,Kouji Matsushima ,Norihiro Tada ,Hiroyasu Nakano

Abstract

Interleukin (IL)-11 is a member of the IL-6 family of cytokines and is involved in multiple cellular responses, including tumor development. However, the origin and functions of IL-11-producing (IL-11+) cells are not fully understood. To characterize IL-11+ cells in vivo, we generate Il11 reporter mice. IL-11+ cells appear in the colon in murine tumor and acute colitis models. Il11ra1 or Il11 deletion attenuates the development of colitis-associated colorectal cancer. IL-11+ cells express fibroblast markers and genes associated with cell proliferation and tissue repair. IL-11 induces the activation of colonic fibroblasts and epithelial cells through phosphorylation of STAT3. Human cancer database analysis reveals that the expression of genes enriched in IL-11+ fibroblasts is elevated in human colorectal cancer and correlated with reduced recurrence-free survival. IL-11+ fibroblasts activate both tumor cells and fibroblasts via secretion of IL-11, thereby constituting a feed-forward loop between tumor cells and fibroblasts in the tumor microenvironment.

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