Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 22, Issue 9, Pages -Publisher
MDPI
DOI: 10.3390/ijms22094750
Keywords
ARID1A; OCCC; mitochondria; ovarian cancer
Funding
- US Department of Defense Ovarian Cancer Research Program [OC160377]
- Minnesota Ovarian Cancer Alliance
- Randy Shaver Cancer Research and Community Fund
- National Institute of General Medical Sciences [R01-GM130800]
- Cancerfonden
- Vetenskapsradet
- Radiumhemmets forskningsfonder
- Knut och Alice Wallenbergs Stiftelse
- Linkoping Cancer Network
- CDMRP [OC160377, 917602] Funding Source: Federal RePORTER
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Ovarian clear cell carcinoma (OCCC) is a rare and chemorefractory tumor with about 50% of patients having inactivating mutations in the ARID1A gene. Loss of ARID1A leads to increased mitochondrial metabolism in OCCC cells, making them more dependent on mitochondrial activity. Preclinical testing has shown that targeting mitochondrial activity can extend overall survival in ARID1A-mutated OCCC.
Ovarian clear cell carcinoma (OCCC) is a rare but chemorefractory tumor. About 50% of all OCCC patients have inactivating mutations of ARID1A, a member of the SWI/SNF chromatin-remodeling complex. Members of the SWI/SNF remodeling have emerged as regulators of the energetic metabolism of mammalian cells; however, the role of ARID1A as a modulator of the mitochondrial metabolism in OCCCs is yet to be defined. Here, we show that ARID1A loss results in increased mitochondrial metabolism and renders ARID1A-mutated cells increasingly and selectively dependent on it. The increase in mitochondrial activity following ARID1A loss is associated with increase in c-Myc expression and increased mitochondrial number and reduction of their size consistent with a higher mitochondrial cristae/outer membrane ratio. Significantly, preclinical testing of the complex I mitochondrial inhibitor IACS-010759 showed it extends overall survival in a preclinical model of ARID1A-mutated OCCC. These findings provide for the targeting mitochondrial activity in ARID1A-mutated OCCCs.
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