GPR56/ADGRG1 Inhibits Mesenchymal Differentiation and Radioresistance in Glioblastoma
Author(s) -
Marta Fernández,
Leire Pedrosa,
Laia Paré,
Estela Pineda,
Leire Bejarano,
Josefina Martínez,
Veerakumar Balasubramaniyan,
Ravesanker Ezhilarasan,
Naveen Kallarackal,
Sung-Hak Kim,
Jia Wang,
Alessandra Audia,
Siobhan Conroy,
Mercedes MarínAguilera,
Teresa Ribalta,
Teresa Pujol,
Antoni Herreros,
Avelina Tortosa,
Helena Mira,
Marta M. Alonso,
Candelaria GomezManzano,
Francesc Graus,
Erik P. Sulman,
Xianhua Piao,
Ichiro Nakano,
Aleix Prat,
Krishna Bhat,
Núria de la Iglesia
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.10.083
Subject(s) - radioresistance , mesenchymal stem cell , cancer research , biology , epithelial–mesenchymal transition , glioma , microbiology and biotechnology , cancer , cell culture , metastasis , genetics
A mesenchymal transition occurs both during the natural evolution of glioblastoma (GBM) and in response to therapy. Here, we report that the adhesion G-protein-coupled receptor, GPR56/ADGRG1, inhibits GBM mesenchymal differentiation and radioresistance. GPR56 is enriched in proneural and classical GBMs and is lost during their transition toward a mesenchymal subtype. GPR56 loss of function promotes mesenchymal differentiation and radioresistance of glioma initiating cells both in vitro and in vivo. Accordingly, a low GPR56-associated signature is prognostic of a poor outcome in GBM patients even within non-G-CIMP GBMs. Mechanistically, we reveal GPR56 as an inhibitor of the nuclear factor kappa B (NF-κB) signaling pathway, thereby providing the rationale by which this receptor prevents mesenchymal differentiation and radioresistance. A pan-cancer analysis suggests that GPR56 might be an inhibitor of the mesenchymal transition across multiple tumor types beyond GBM.
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