Flavonoid apigenin modified gene expression associated with inflammation and cancer and induced apoptosis in human pancreatic cancer cells through inhibition of GSK-3β/NF-κB signaling cascade
Flavonoid apigenin modified gene expression associated with inflammation and cancer and induced apoptosis in human pancreatic cancer cells through inhibition of GSK-3β/NF-κB signaling cascade
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DOI:
10.1002/mnfr.201300307
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发表时间:
2013-12-01
影响因子:
5.2
通讯作者:
de Mejia, Elvira Gonzalez
中科院分区:
文献类型:
--
作者:
Johnson, Jodee L.;de Mejia, Elvira Gonzalez
ScopeThe objective was to examine the inhibitory effects of citrus fruit bioactive compounds on BxPC-3 and PANC-1 human pancreatic cancer cells, focusing on the antiproliferative mechanism of action of the flavonoid apigenin related to the glycogen synthase kinase-3/nuclear factor kappa B signaling pathway.Methods and resultsFlavonoids, limonoids, phenolic acids, and ascorbic acid were tested for cytotoxic effects on BxPC-3 and PANC-1 cells; apigenin was the most potent (IC50 = 23 and 12 M for 24 and 48 h for BxPC-3 and IC50 = 71 and 41 M for 24 and 48 h for PANC-1). Apigenin induced pancreatic cell death through inhibition of the glycogen synthase kinase-3/nuclear factor kappa B signaling pathway. Apigenin arrested cell cycle at G(2)/M phase (36 and 32% at 50 M for BxPC-3 and PANC-1, respectively) with concomitant decrease in the expression of cyclin B1. Apigenin activated the mitochondrial pathway of apoptosis (44 and 14% at 50 M for BxPC-3 and PANC-1, respectively) and modified the expression of apoptotic proteins. Apigenin highly upregulated the expression of cytokine genes IL17F (114.2-fold), LTA (33.1-fold), IL17C (23.2-fold), IL17A (11.3-fold), and IFNB1 (8.9-fold) in BxPC-3 cells, which potentially contributed to the anticancer properties.ConclusionFlavonoids have a protective role in pancreatic cancer tumorigenesis.