Conjugated linolenic fatty acids trigger ferroptosis in triple-negative breast cancer

Beatty, A.; Singh, T.; Tyurina, Y. Y.; Nicolas, E.; Maslar, K.; Zhou, Y.; Cai, K. Q.; Tan, Y.; Doll, S.; Conrad, M.; Bayır, H.; Kagan, V. E.; Rennefahrt, U.; Peterson, J. R.

doi:10.1101/556084

bioRxiv · 10.1101/556084

Conjugated linolenic fatty acids trigger ferroptosis in triple-negative breast cancer

Beatty, A.·Singh, T.·Tyurina, Y. Y.·Nicolas, E.·Maslar, K.·Zhou, Y.·Cai, K. Q.·Tan, Y.·Doll, S.·Conrad, M.·Bayır, H.·Kagan, V. E.·Rennefahrt, U.·Peterson, J. R.

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Abstract

Ferroptosis is a non-apoptotic form of cell death linked to the accumulation of reactive hydroperoxides generated by oxidation of polyunsaturated fatty acids (PUFAs) in membrane phospholipids. The therapeutic potential of promoting ferroptosis by enriching PUFAs in cancer cells is unknown. We found an association between elevated PUFA levels and vulnerability to ferroptosis in triple-negative breast cancer (TNBC) cells. A screen of PUFAs identified conjugated linolenic acids, including -eleostearate, as ferroptosis inducers. Three conjugated double bonds were required for ferroptotic activity although their positioning and stereochemistry were less significant. Mechanistically, -eleostearate differed from canonical ferroptosis inducers by a distinct dependence on acyl-CoA synthetase long-chain isoforms and by not altering glutathione or glutathione peroxidase 4 activity. Orally administered tung oil, naturally rich in -eleostearate, limited tumor growth and metastasis in an aggressive TNBC xenograft model. These results expand our understanding of ferroptotic cell death and highlight the anti-cancer potential of conjugated PUFAs.

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Beatty, A., Singh, T., Tyurina, Y. Y., Nicolas, E., Maslar, K., Zhou, Y., Cai, K. Q., Tan, Y., Doll, S., Conrad, M., Bayır, H., Kagan, V. E., Rennefahrt, U., Peterson, J. R.. 2019-02-20. Conjugated linolenic fatty acids trigger ferroptosis in triple-negative breast cancer. https://doi.org/10.1101/556084

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