TY - JOUR T1 - A Syx-RhoA-Dia1 signaling axis regulates cell cycle progression, DNA damage, and therapy resistance in glioblastoma JF - bioRxiv DO - 10.1101/2021.12.03.469255 SP - 2021.12.03.469255 AU - Wan-Hsin Lin AU - Ryan W. Feathers AU - Lisa M. Cooper AU - Laura J. Lewis-Tuffin AU - Jann N. Sarkaria AU - Panos Z. Anastasiadis Y1 - 2021/01/01 UR - http://biorxiv.org/content/early/2021/12/03/2021.12.03.469255.abstract N2 - Glioblastomas (GBM) are aggressive tumors that lack effective treatments. Here, we show that the Rho family guanine nucleotide exchange factor Syx promotes GBM cell growth both in vitro and in orthotopic GBM patient-derived xenografts. Growth defects upon Syx depletion are attributed to prolonged mitosis, increased DNA damage, G2/M cell cycle arrest, and cell apoptosis, mediated by altered mRNA and protein expression of various cell cycle regulators. These effects are phenocopied by depletion of the Rho downstream effector Dia1 and are due at least in part to increased cytoplasmic retention and reduced activity of the YAP/TAZ transcriptional coactivators. Further, targeting Syx signaling cooperates with radiation treatment and temozolomide (TMZ) to decrease viability in GBM cells irrespective of their inherent response to TMZ. Taken together, the data indicate that a Syx-RhoA-Dia1-YAP/TAZ signaling axis regulates cell cycle progression, DNA damage, and therapy resistance in GBM and argue for its targeting for cancer treatment.One Sentence Summary Syx promotes growth and therapy resistance in glioblastoma.Competing Interest StatementThe authors have declared no competing interest. ER -