A sensitized RNA interference screen identifies a novel role for the PI3K p110I-gamma isoform in medulloblastoma cell proliferation and chemoresistance

Ana Guerreiro, Sarah Fattet, Dorota Kulesza, Abdullah Atamer, Alexandra Elsing, Tarek Shalaby, Shaun Jackson, Simone Schoenwaelder, Michael Grotzer, Olivier Delattre, Alexandre Arcaro

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Abstract

Medulloblastoma is the most common malignant brain tumor in children and is associated with a poor outcome. We were interested in gaining further insight into the potential of targeting the human kinome as a novel approach to sensitize medulloblastoma to chemotherapeutic agents. A library of small interfering RNA (siRNA) was used to downregulate the known human protein and lipid kinases in medulloblastoma cell lines. The analysis of cell proliferation, in the presence or absence of a low dose of cisplatin after siRNA transfection, identified new protein and lipid kinases involved in medulloblastoma chemoresistance. PLK1 (polo-like kinase 1) was identified as a kinase involved in proliferation in medulloblastoma cell lines. Moreover, a set of 6 genes comprising ATR, LYK5, MPP2, PIK3CG, PIK4CA, and WNK4 were identified as contributing to both cell proliferation and resistance to cisplatin treatment in medulloblastoma cells. An analysis of the expression of the 6 target genes in primary medulloblastoma tumor samples and cell lines revealed overexpression of LYK5 and PIK3CG. The results of the siRNA screen were validated by target inhibition with specific pharmacological inhibitors. A pharmacological inhibitor of p110I? (encoded by PIK3CG) impaired cell proliferation in medulloblastoma cell lines and sensitized the cells to cisplatin treatment. Together, our data show that the p110I? phosphoinositide 3-kinase isoform is a novel target for combinatorial therapies in medulloblastoma. A?2011 AACR.
Original languageEnglish
Pages (from-to)925 - 935
Number of pages11
JournalMolecular Cancer Research
Volume9
Issue number7
DOIs
Publication statusPublished - 2011

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