부산대학교 도서관

Dysregulation of the PI3K/AKT pathway is a common occurrence in high‐grade serous ovarian carcinoma (HGSOC), with the loss of the tumour suppressor PTEN in HGSOC being associated with poor prognosis. The cellular mechanisms of how PTEN loss contributes to HGSOC are largely unknown. We here utilise time‐lapse imaging of HGSOC spheroids coupled to a machine learning approach to classify the phenotype of PTEN loss. PTEN deficiency induces PI(3,4,5)P3‐rich and ‐dependent membrane protrusions into the extracellular matrix (ECM), resulting in a collective invasion phenotype. We identify the small GTPase ARF6 as a crucial vulnerability of HGSOC cells upon PTEN loss. Through a functional proteomic CRISPR screen of ARF6 interactors, we identify the ARF GTPase‐activating protein (GAP) AGAP1 and the ECM receptor β1‐integrin (ITGB1) as key ARF6 interactors in HGSOC regulating PTEN loss‐associated invasion. ARF6 functions to promote invasion by controlling the recycling of internalised, active β1‐integrin to maintain invasive activity into the ECM. The expression of the CYTH2‐ARF6‐AGAP1 complex in HGSOC patients is inversely associated with outcome, allowing the identification of patient groups with improved versus poor outcome. ARF6 may represent a therapeutic vulnerability in PTEN‐depleted HGSOC. Synopsis: Loss of the tumor suppressor PTEN is associated with poor prognosis in high‐grade serous ovarian carcinoma (HGSOC) but its cellular role remains unclear. Here, PTEN deficiency is shown to drive PI(3,4,5)P3‐dependent cancer cell invasion via enhancing recycling of pro‐invasive endocytic cargos. PTEN depletion in three‐dimensional HGSOC spheroids induces PI(3,4,5)P3‐rich membrane protrusions in an ARF6‐dependent manner.A CYTH2‐ARF6‐AGAP1 module regulates PTEN loss‐associated invasion, with GEF CYTH2 being PI(3,4,5)P3‐responsive.The CYTH2‐ARF6‐AGAP1 module localises to PI(3,4,5)P3‐rich protrusion tips, supporting recycling of β1‐integrin and extracellular matrix invasion.Expression of the ARF6 complex in HGSOC patients is inversely correlated with outcome. [ABSTRACT FROM AUTHOR]