Abstract
There is little doubt that prostanoids are involved in the development of many types of cancer (1, 2). However, their role is not a simple one, and is poorly understood. Prostanoids, particularly PGE2, can promote the development of tumors, enhance the effects of initiators such as phorbol esters, promote tumor cell growth and spread, stimulate bone breakdown and inhibit the immune response (3). However, PGE2 also has the capacity to cause the opposite effects (4). It is not surprising, therefore, that studies with inhibitors of the endogenous synthesis of prostanoids such as the NSAIDs have given conflicting results, and have been generally disappointing in cancer therapy.
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Coleman, R.A. (1993). Prostanoids, Prostanoid Receptors and Tumor Progression. In: Nigam, S., Honn, K.V., Marnett, L.J., Walden, T.L. (eds) Eicosanoids and Other Bioactive Lipids in Cancer, Inflammation and Radiation Injury. Developments in Oncology, vol 71. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3520-1_30
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DOI: https://doi.org/10.1007/978-1-4615-3520-1_30
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