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Published on: March 22, 2012
Targeting sphingolipid metabolism as an approach for combination therapies in haematological malignancies
Alexander C Lewis1, Craig T Wallington-Beddoe1,2,3,4, Jason A Powell1,2
1Centre for Cancer Biology, University of South Australia and SA Pathology, UniSA CRI Building, North Terrace, Adelaide, SA, 5001, Australia.
Abstract:
Conventional chemotherapy-based drug combinations have, until recently, been the backbone of most therapeutic strategies for cancer. In a time of emerging rationale drug development, targeted therapies are beginning to be added to traditional chemotherapeutics to synergistically enhance clinical responses. Of note, the importance of pro-apoptotic ceramide in mediating the anti-cancer effects of these therapies is becoming more apparent. Furthermore, reduced cellular ceramide in favour of pro-survival sphingolipids correlates with tumorigenesis and most importantly, drug resistance. Thus, agents that manipulate sphingolipid metabolism have been explored as potential anti-cancer agents and have recently demonstrated exciting potential to augment the efficacy of anti-cancer therapeutics. This review examines the biology underpinning these observations and the potential use of sphingolipid manipulating agents in the context of existing and emerging therapies for haematological malignancies.
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