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Curcumin suppresses proliferation and invasion in human gastric cancer cells by downregulation of PAK1 activity and cyclin Dl expression

机译:姜黄素通过下调PAK1活性和cyclin Dl表达抑制人胃癌细胞的增殖和侵袭

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Curcumin (diferuloylmethane), is a natural chemopreventive agent known to inhibit the proliferation of several cancer cell lines. It has been previously demonstrated that curcumin is a potent inhibitor of EGF-receptor (EGFR) tyrosine kinase, but its inhibitive effect on p21-activated kinase 1 (PAKl), a downstream protein of EGFR, has not been defined. In this paper we found that curcumin repressed the expression of HER2 and inhibited the kinase activity of PAKl without affecting its expression. Silencing HER2 in gastric cancer cells showed that even if PAKl activity was transiently strengthened by EGF, curcumin still had a strong inhibitive effect. It should be emphasized that kinase assay in vitro showed that curcumin could act as an ATP-competitive inhibitor, which was supported by computer-aided molecular modeling. Curcumin also downregulated the mRNA and the protein expression of cyclin Dl and suppressed transition of the cells from Gx to S phase. Therefore, curcumin inhibited the proliferation and invasion of gastric cancer cells. Overall, these results provided novel insights into the mechanisms of curcumin inhibition of gastric cancer cell growth and potential therapeutic strategies for gastric cancer.
机译:姜黄素(二氟甲酰甲烷)是一种天然的化学预防剂,已知可以抑制几种癌细胞的增殖。以前已经证明姜黄素是EGF受体(EGFR)酪氨酸激酶的有效抑制剂,但是尚未确定其对p21活化激酶1(PAK1)(EGFR的下游蛋白)的抑制作用。在本文中,我们发现姜黄素可抑制HER2的表达并抑制PAK1的激酶活性,而不会影响其表达。使胃癌细胞中的HER2沉默表明,即使EGF瞬时增强了PAK1活性,姜黄素仍具有很强的抑制作用。应该强调的是,体外激酶测定表明姜黄素可以作为ATP竞争性抑制剂,这得到了计算机辅助分子模型的支持。姜黄素还下调细胞周期蛋白D1的mRNA和蛋白表达,并抑制细胞从Gx过渡到S期。因此,姜黄素抑制胃癌细胞的增殖和侵袭。总体而言,这些结果为姜黄素抑制胃癌细胞生长的机制和潜在的胃癌治疗策略提供了新颖的见解。

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