4.8 Article

R-Spondin1/LGR5 Activates TGFβ Signaling and Suppresses Colon Cancer Metastasis

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CANCER RESEARCH
卷 77, 期 23, 页码 6589-6602

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-17-0219

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  1. NIH/NCI [R01CA215389, R01CA212241, R01CA208063, R15GM122006]
  2. Fred and Pamela Buffett Cancer Center [P30 CA036727]
  3. Nebraska Research Initiative
  4. NIH/NIGMS [P30 GM106397]

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Leucine-rich repeat containing G-protein-coupled receptor 5 (LGR5), an intestinal stem cell marker, is known to exhibit tumor suppressor activity in colon cancer, the mechanism of which is not understood. Here we show that R-spondin 1 (RSPO1)/LGR5 directly activates TGF beta signaling cooperatively with TGF beta type II receptor in colon cancer cells, enhancing TGF beta-mediated growth inhibition and stress-induced apoptosis. Knockdown of LGR5 attenuated downstream TGF beta signaling and increased cell proliferation, survival, and metastasis in an orthotopic model of colon cancer in vivo. Upon RSPO1 stimulation, LGR5 formed complexes with TGF beta receptors. Studies of patient specimens indicate that LGR5 expression was reduced in advanced stages and positively correlated with markers of TGFb activation in colon cancer. Our study uncovers a novel cross-talk between LGR5 and TGFb signaling in colon cancer and identifies LGR5 as a new modulator of TGFb signaling able to suppress colon cancer metastasis. (C) 2017 AACR.

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