Cell Death Discovery · 2021 · 80 citations · 48 references
MedicineOncologyPharmacologyCell SignalingMolecular OncologySignal TransductionBile Acid MetabolismCancer Cell SignalingColorectal CancerOncogenic Signaling PathwaysSignal Transduction In CancerTumor Suppressor GenesBile Acid ReceptorsBile Acid-mediated CarcinogenesisHippo Signaling PathwayIntestinal Bile Acid MetabolismMalignant ProgressionTgr5 SignalingYap SignalingYes-associated Protein Signaling
The Hippo/YAP pathway plays an important role in the development of cancers. Previous studies have reported that bile acids can activate YAP (Yes Associated Protein) to promote tumorigenesis and tumor progression. Ursodeoxycholic acid (UDCA) is a long-established old drug used for cholestasis treatment. So far, the effect of UDCA on YAP signaling in colorectal cancer (CRC) is not well defined. This study means to explore relationship of UDCA and YAP in CRC. UDCA suppressed YAP signaling by activating the membrane G-protein-coupled bile acid receptor (TGR5). TGR5 mainly regulated cAMP/PKA signaling pathway to inhibit RhoA activity, thereby suppressing YAP signaling. Moreover, the restoration of YAP expression alleviated the inhibitory effect of UDCA on CRC cell proliferation. In AOM/DSS-induced CRC model, UDCA inhibited tumor growth in a concentration-dependent manner and decreased expression of YAP and Ki67. UDCA plays a distinguished role in regulating YAP signaling and CRC growth from the primary bile acids and partial secondary bile acids, demonstrating the importance of maintaining normal intestinal bile acid metabolism in cancer patients. It also presents a potential therapeutic intervention for CRC.
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Metabolic control of YAP and TAZ by the mevalonate pathway
Giovanni Sorrentino, Naomi Ruggeri, Valeria Specchia et al. · Nature Cell Biology · 2014 · 774 citations
Alternative Wnt Signaling Activates YAP/TAZ
Hyun Woo Park, Young Chul Kim, Bo Yu et al. · Cell · 2015 · 736 citations · Full text