Journal article

Publication year: 2021

Pages: 422-434

Journal: Clinical and Experimental Pharmacology and Physiology

Volume number: 48

Issue number: 3

ISSN: 0305-1870

eISSN: 1440-1681

Open access status: Hybrid

DOI Link: https://doi.org/10.1111/1440-1681.13452

Publisher: Wiley

Abstract: 
Nicotinamide phosphoribosyltransferase (NAMPT) is a rate-limiting enzyme for nicotinamide adenine dinucleotide (NAD) synthesis and is involved in cancer cell proliferation through regulation of energy production pathways. Therefore, NAMPT inhibitors are promising drugs for cancer therapy by limiting energy supply of tumours. Herein, we demonstrated that the NAMPT inhibitor FK866 ((E)-N-(4-(1-Benzoylpiperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamide) dose-dependently inhibited growth and cell motility of DU-145 prostate tumour spheroids and decreased the intracellular ATP concentration. The apoptosis marker cleaved caspase-3 remained unchanged, but the autophagy marker microtubule-associated protein 1A/1B-light chain 3 (LC3) was upregulated. Growth inhibition was reversed upon co-administration of NAD to the cell culture medium. FK866 decreased calcein as well as pheophorbide A efflux from tumour spheroids and increased doxorubicin toxicity, indicating interference with function of drug efflux transporters. DU-145 multicellular tumour spheroids expressed the stem cell associated markers CD133, CD44, Oct4, Nanog, Sox2, and drug transporters ABCB1, ABCG2, and ABCC1 which are associated with stem cell properties in cancer cells. The ABCB1 inhibitor zosuquidar, the ABCG2 inhibitor Ko143, and the ABCC1 inhibitor MK571 increased calcein retention. Neither protein expression of stem cell markers, nor drug transporters was significantly changed upon FK866 treatment. In conclusion, our data suggest that FK866 inhibits prostate cancer cell proliferation by interference with the energy metabolism, and function of drug efflux transporters.

Harvard Citation style: Sauer, H., Kampmann, H., Kosravi, F., Sharifpanah, F. and Wartenberg, M. (2021) The nicotinamide phosphoribosyltransferase antagonist FK866 inhibits growth of prostate tumour spheroids and increases doxorubicin retention without changes in drug transporter and cancer stem cell protein expression, Clinical and Experimental Pharmacology and Physiology, 48(3), pp. 422-434. https://doi.org/10.1111/1440-1681.13452

APA Citation style: Sauer, H., Kampmann, H., Kosravi, F., Sharifpanah, F., & Wartenberg, M. (2021). The nicotinamide phosphoribosyltransferase antagonist FK866 inhibits growth of prostate tumour spheroids and increases doxorubicin retention without changes in drug transporter and cancer stem cell protein expression. Clinical and Experimental Pharmacology and Physiology. 48(3), 422-434. https://doi.org/10.1111/1440-1681.13452