RHOA L57V drives the development of diffuse gastric cancer through IGF1R-PAK1-YAP1 signaling

• Published in: Science signaling Vol. 16; no. 816; p. eadg5289
• Main Authors: Schaefer, Antje, Hodge, Richard G, Zhang, Haisheng, Hobbs, G Aaron, Dilly, Julien, Huynh, Minh V, Goodwin, Craig M, Zhang, Feifei, Diehl, J Nathaniel, Pierobon, Mariaelena, Baldelli, Elisa, Javaid, Sehrish, Guthrie, Karson, Rashid, Naim U, Petricoin, Emanuel F, Cox, Adrienne D, Hahn, William C, Aguirre, Andrew J, Bass, Adam J, Der, Channing J
• Format: Journal Article
• Language: English
• Published: United States 19.12.2023
• Subjects: Actins; Animals; Guanosine Triphosphate; Humans; Mice; p21-Activated Kinases; Proto-Oncogene Proteins p21(ras); Receptor, IGF Type 1; rhoA GTP-Binding Protein - genetics; Signal Transduction; Stomach Neoplasms - genetics
• ISSN: 1937-9145
• DOI: 10.1126/scisignal.adg5289

Cancer-associated mutations in the guanosine triphosphatase (GTPase) RHOA are found at different locations from the mutational hotspots in the structurally and biochemically related RAS. Tyr -to-Cys (Y42C) and Leu -to-Val (L57V) substitutions are the two most prevalent RHOA mutations in diffuse gastric cancer (DGC). RHOA exhibits a gain-of-function phenotype and is an oncogenic driver in DGC. Here, we determined how RHOA promotes DGC growth. In mouse gastric organoids with deletion of , which encodes the cell adhesion protein E-cadherin, the expression of RHOA , but not of wild-type RHOA, induced an abnormal morphology similar to that of patient-derived DGC organoids. RHOA also exhibited a gain-of-function phenotype and promoted F-actin stress fiber formation and cell migration. RHOA retained interaction with effectors but exhibited impaired RHOA-intrinsic and GAP-catalyzed GTP hydrolysis, which favored formation of the active GTP-bound state. Introduction of missense mutations at KRAS residues analogous to Tyr and Leu in RHOA did not activate KRAS oncogenic potential, indicating distinct functional effects in otherwise highly related GTPases. Both RHOA mutants stimulated the transcriptional co-activator YAP1 through actin dynamics to promote DGC progression; however, RHOA additionally did so by activating the kinases IGF1R and PAK1, distinct from the FAK-mediated mechanism induced by RHOA . Our results reveal that RHOA and RHOA drive the development of DGC through distinct biochemical and signaling mechanisms.