Sambantham Shanmugam, Radha Mahendran, Paramasivam Arumugam, Anandan Balakrishnan, Malathi Ragunathan, Chandra Samuel Rajkumar, Jayaraman Gopalswamy
Department of Genetics, University of Madras, Chennai, India.
Asian Pac J Cancer Prev. 2013;14(7):4347-52. doi: 10.7314/apjcp.2013.14.7.4347.
To investigate the molecular mechanisms underlying triggering of apoptosis by hesperetin using in silico and in vitro methods.
The mechanism of binding of hesperetin with NF-?B and other apoptotic proteins like BAX, BAD, BCL2 and BCLXL was analysed in silico using Schrodinger suite 2009. In vitro studies were also carried out to evaluate the potency of hesperetin in inducing apoptosis using the human prostate cancer PC-3 cell line.
Hesperetin was found to exhibit high-affinity binding resulting from greater intermolecular forces between the ligand and its receptor NF-?B (-7.48 Glide score). In vitro analysis using MTT assay confirmed that hesperetin reduced cell proliferation (IC50 values of 90 and 40μM at 24 and 48h respectively) in PC-3 cells. Hesperetin also downregulated expression of the anti-apoptotic gene BCLXL at both mRNA and protein levels and increased the expression of pro-apoptotic genes like BAD at mRNA level and BAX at mRNA as well as protein levels.
The results suggest that hesperetin can induce apoptosis by inhibiting NF-?B.
采用计算机模拟和体外实验方法,研究橙皮素引发细胞凋亡的分子机制。
使用Schrodinger suite 2009软件对橙皮素与核因子κB(NF-κB)以及其他凋亡蛋白(如BAX、BAD、BCL2和BCLXL)的结合机制进行计算机模拟分析。还进行了体外实验,使用人前列腺癌PC-3细胞系评估橙皮素诱导细胞凋亡的能力。
发现橙皮素表现出高亲和力结合,这是由于配体与其受体NF-κB之间存在更强的分子间作用力(-7.48 Glide评分)。使用MTT法进行的体外分析证实,橙皮素可降低PC-3细胞的增殖(在24小时和48小时时的IC50值分别为90和40μM)。橙皮素还在mRNA和蛋白质水平下调抗凋亡基因BCLXL的表达,并在mRNA水平上调促凋亡基因BAD的表达,在mRNA和蛋白质水平上调BAX的表达。
结果表明,橙皮素可通过抑制NF-κB诱导细胞凋亡。