R-Spondin1/LGR5 Activates TGFβ Signaling and Suppresses Colon Cancer Metastasis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28939678.
- Also identified by DOI 10.1158/0008-5472.CAN-17-0219 and PMC identifier 5898809.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
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 TGFβ signaling cooperatively with TGFβ type II receptor in colon cancer cells, enhancing TGFβ-mediated growth inhibition and stress-induced apoptosis. Knockdown of LGR5 attenuated downstream TGFβ signaling and increased cell proliferation, survival, and metastasis in an orthotopic model of colon cancer <i>in vivo</i> Upon RSPO1 stimulation, LGR5 formed complexes with TGFβ receptors. Studies of patient specimens indicate that LGR5 expression was reduced in advanced stages and positively correlated with markers of TGFβ activation in colon cancer. Our study uncovers a novel cross-talk between LGR5 and TGFβ signaling in colon cancer and identifies LGR5 as a new modulator of TGFβ signaling able to suppress colon cancer metastasis. <i>Cancer Res; 77(23); 6589-602. ©2017 AACR</i>.
Medical subject headings
- Colonic Neoplasms
- Neoplasm Metastasis
- Receptors, G-Protein-Coupled
- Thrombospondins
- Transforming Growth Factor beta
- Wnt Signaling Pathway