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AuthorKuttikrishnan, Shilpa
AuthorBhat, Ajaz A.
AuthorMateo, Jericha M.
AuthorAhmad, Fareed
AuthorAlali, Feras Q.
AuthorEl-Elimat, Tamam
AuthorOberlies, Nicholas H.
AuthorPearce, Cedric J.
AuthorUddin, Shahab
Available date2023-05-10T03:43:46Z
Publication Date2022-04-23
Publication NameBiochemical and Biophysical Research Communications
Identifierhttp://dx.doi.org/10.1016/j.bbrc.2022.02.071
CitationKuttikrishnan S, Bhat AA, Mateo JM, Ahmad F, Alali FQ, El-Elimat T, Oberlies NH, Pearce CJ, Uddin S. Anticancer activity of Neosetophomone B by targeting AKT/SKP2/MTH1 axis in leukemic cells. Biochem Biophys Res Commun. 2022 Apr 23;601:59-64. doi: 10.1016/j.bbrc.2022.02.071.
ISSN0006291X
URIhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85126115788&origin=inward
URIhttp://hdl.handle.net/10576/42517
AbstractNeosetophomone B (NSP–B), a meroterpenoid fungal secondary metabolite, was investigated for its anticancer potential in leukemic cell lines (K562 and U937). NSP-B treatment of leukemic cells suppressed cell viability by triggering apoptotic cell death. Apoptosis induced by NSP-B is triggered by mitochondrial signaling and caspase activation. Additionally, NSP-B treatment of leukemic cells causes AKT's inactivation accompanied by downregulation of SKP2 oncogene and MTH1 with a concomitant increase of p21Cip1and p27Kip1. Furthermore, NSP-B causes suppression of antiapoptotic proteins, including cIAP1, cIAP2, XIAP, survivin and BCl-XL. Overall, NSP-B reduces cell viability by mitochondrial and caspase-dependent apoptosis. The inhibition of AKT and SKP2 axis could be a promising therapeutic target for leukemia treatment.
SponsorThis work was supported by grant funded by the Medical Research Center (MRC), Hamad Medical Corporation, Doha, Qatar (MRC-01-21-301). The authors thank Qatar National Library for open access support of this article.
Languageen
PublisherElsevier
SubjectApoptosis
Fungal secondary metabolites
Leukemia
Meroterpenoids
Natural products
Neosetophomone B
TitleAnticancer activity of Neosetophomone B by targeting AKT/SKP2/MTH1 axis in leukemic cells
TypeArticle
Pagination59-64
Volume Number601
dc.accessType Open Access


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