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 PMID:25625625  

Coexistent ARID1A-PIK3CA mutations promote ovarian clear-cell tumorigenesis through pro-tumorigenic inflammatory cytokine signalling.

Ronald L Chandler | Jeffrey S Damrauer | Jesse R Raab | Jonathan C Schisler | Matthew D Wilkerson | John P Didion | Joshua Starmer | Daniel Serber | Della Yee | Jessie Xiong | David B Darr | Fernando Pardo-Manuel de Villena | William Y Kim | Terry Magnuson
Nature communications | 2015

Ovarian clear-cell carcinoma (OCCC) is an aggressive form of ovarian cancer with high ARID1A mutation rates. Here we present a mutant mouse model of OCCC. We find that ARID1A inactivation is not sufficient for tumour formation, but requires concurrent activation of the phosphoinositide 3-kinase catalytic subunit, PIK3CA. Remarkably, the mice develop highly penetrant tumours with OCCC-like histopathology, culminating in haemorrhagic ascites and a median survival period of 7.5 weeks. Therapeutic treatment with the pan-PI3K inhibitor, BKM120, prolongs mouse survival by inhibiting the tumour cell growth. Cross-species gene expression comparisons support a role for IL-6 inflammatory cytokine signalling in OCCC pathogenesis. We further show that ARID1A and PIK3CA mutations cooperate to promote tumour growth through sustained IL-6 overproduction. Our findings establish an epistatic relationship between SWI/SNF chromatin remodelling and PI3K pathway mutations in OCCC and demonstrate that these pathways converge on pro-tumorigenic cytokine signalling. We propose that ARID1A protects against inflammation-driven tumorigenesis.

Pubmed ID: 25625625

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: R01 HD036655
  • Agency: NCI NIH HHS, United States
    Id: CA142794
  • Agency: NICHD NIH HHS, United States
    Id: HD03665
  • Agency: NCI NIH HHS, United States
    Id: R01 CA142794
  • Agency: NHLBI NIH HHS, United States
    Id: T32-HL069768
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL069768

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