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

Takashi Nishina(Toho University), Yutaka Deguchi(Toho University), Daisuke Ohshima(Toho University), Wakami Takeda(Toho University), Masato Ohtsuka(Tokai University), Shigeyuki Shichino(Tokyo University of Science), Satoshi Ueha(Tokyo University of Science), Soh Yamazaki(Toho University), Mika Kawauchi(Toho University), Eri Nakamura(Juntendo University), Chiharu Nishiyama(Tokyo University of Science), Yuko Kojima(Juntendo University), Satomi Adachi‐Akahane(Toho University), Mizuho Hasegawa(University of Michigan), Mizuho Nakayama(Kanazawa University), Masanobu Oshima(Kanazawa University), Hideo Yagita∥(Juntendo University), Kazutoshi Shibuya(Toho University), Tetuo Mikami(Toho University), Naohiro Inohara(University of Michigan), Kouji Matsushima(Tokyo University of Science), Norihiro Tada(Juntendo University), Hiroyasu Nakano(Toho University)
Nature Communications
April 16, 2021
Cited by 130Open Access
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Abstract

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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