Growth suppression and cell death by pyridoxal is dependent on p53 in the human breast cancer cell line MCF-7

被引:7
|
作者
Minamino, Masaki [1 ]
Oka, Tatsuzo [1 ]
Kanouchi, Hiroaki [1 ]
机构
[1] Kagoshima Univ, Joint Fac Vet Med, Dept Vet Pathobiol, Kagoshima 890, Japan
关键词
vitamin B-6; pyridoxal; MCF-7; p53; insulin-like growth factor binding protein-3 (IGFBP-3); COLON TUMORIGENESIS; BINDING PROTEIN-3; VITAMIN-B6; MICE; PROLIFERATION; EXPRESSION; APOPTOSIS; IGFBP-3; PATHWAY; GENE;
D O I
10.1080/09168451.2014.952618
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vitamin B-6 compound, pyridoxine (PN), has shown antitumor action. Our previous experiments showed that PN induces expression of insulin-like growth factor binding protein-3 to arrest proliferation and induce cell death. This induction is inhibited by the p53-specific inhibitor pifithrin-alpha. Here, we report that another B-6 compound, pyridoxal (PL), strongly inhibited MCF-7 cell growth compared to PN. PL induced the G(0)/G(1) arrest and the accumulation of subG1 population. Although p53 mRNA was not changed by PL, 0.5mM PL increased the protein level in MCF-7 cells. The cell growth suppression by 0.5mM PL did not occur when p53 expression was knocked down using siRNA. Together, these data suggest that PL accumulate p53 and PL-induced cell growth suppression is dependent on p53 in MCF-7 breast cancer cells.
引用
收藏
页码:124 / 129
页数:6
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