ATM-deficient lung, prostate and pancreatic cancer cells are acutely sensitive to the combination of olaparib and the ATR inhibitor AZD6738

Jette, N. R.; Radhamani, S.; Ye, R.; Yu, Y.; Arthur, G.; Goutam, S.; Bizmar, T.; Kumar, M.; Bose, P.; Yip, S.; Kolinsky, M.; Lees-MIller, S. P.

doi:10.1101/2020.03.13.991166

bioRxiv · 10.1101/2020.03.13.991166

ATM-deficient lung, prostate and pancreatic cancer cells are acutely sensitive to the combination of olaparib and the ATR inhibitor AZD6738

Jette, N. R.·Radhamani, S.·Ye, R.·Yu, Y.·Arthur, G.·Goutam, S.·Bizmar, T.·Kumar, M.·Bose, P.·Yip, S.·Kolinsky, M.·Lees-MIller, S. P.

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Abstract

BackgroundThe ataxia telangiectasia mutated (ATM) protein kinase is mutated in several human cancers, presenting potential opportunities for targeted cancer therapy. We previously reported that the poly-ADP ribose polymerase (PARP) inhibitor olaparib induced transient G2 arrest but not cell death in ATM-deficient A549 lung cancer cells, while the combination of olaparib with the ATM-, Rad3-related (ATR) inhibitor VE-821 induced cell death. Here, we show that the clinically relevant ATR inhibitor, AZD6738, sensitizes ATM-deficient A549 lung, prostate and pancreatic cancer cells to olaparib. MethodsATM was depleted from A549 lung cancer cells, PC-3 prostate cancer cells and Panc 10.05 pancreatic cancer cells, and the effects of olaparib alone and in combination with AZD6738 were determined. ResultsThe combination of olaparib plus AZD6738 induced cell death in ATM-deficient lung, prostate and pancreatic cancer cells with little effect on their ATM-proficient counterparts. ConclusionsLung, prostate and pancreatic patients whose tumours exhibit loss or inactivation of ATM may benefit from combination of a PARP inhibitor plus an ATR inhibitor.

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Jette, N. R., Radhamani, S., Ye, R., Yu, Y., Arthur, G., Goutam, S., Bizmar, T., Kumar, M., Bose, P., Yip, S., Kolinsky, M., Lees-MIller, S. P.. 2020-03-15. ATM-deficient lung, prostate and pancreatic cancer cells are acutely sensitive to the combination of olaparib and the ATR inhibitor AZD6738. https://doi.org/10.1101/2020.03.13.991166

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