Department of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Balanagar, Hyderabad, Telangana 500037, India.
Centre for Pharmaceutical Sciences, Institute of Science and Technology, Jawaharlal Nehru Technological University, Kukatpally, Hyderabad, Telangana 500085, India.
Toxicol In Vitro. 2018 Sep;51:114-128. doi: 10.1016/j.tiv.2018.05.010. Epub 2018 May 17.
Autophagy is a critical regulator of cellular homeostasis and its dysregulation often results in various disease manifestations, including cancer. Nimbolide, an active chemical constituent of neem (Azadirachta indica) exhibits potent anticancer effects. Although, nimbolide mediated apoptosis activation in breast cancer cells is well known. Nevertheless, its role in autophagy induction mechanism and epigenetic alteration is not explored previously. Our current study intended to bridge the gaps in the existing research by exploring the potential of nimbolide in inducing autophagy, which could counter regulate the transformations in breast cancer. In our studies, nimbolide significantly inhibited the cell proliferation of MDA-MB-231 and MCF-7 cells with IC values of 1.97 ± 0.24 and 5.04 ± 0.25 μM, respectively. Nimbolide markedly arrested the cell cycle progression and cell survival with loss of mitochondrial membrane potential by reducing Bcl-2 concomitantly inducing Bax and caspases protein expression with modulation of HDAC-2 and H3K27Ac expression. Consequently, characteristic autophagolysosome accumulation was observed by acridine orange, monodansylcadaverine (MDC) and Lysotracker Red staining. Moreover, nimbolide induced autophagy signaling by increasing Beclin 1 and LC3B along with decreased p62 and mTOR protein expression. Thus, our findings imply that nimbolide induces autophagy mediated apoptotic cell death in breast cancer with epigenetic modifications.
自噬是细胞内稳态的关键调节因子,其失调通常会导致各种疾病表现,包括癌症。印苦楝素是印楝(Azadirachta indica)的一种活性化学成分,具有很强的抗癌作用。虽然印苦楝素介导的乳腺癌细胞凋亡激活已为人所知,但它在自噬诱导机制和表观遗传改变中的作用以前尚未得到探索。我们目前的研究旨在通过探索印苦楝素在诱导自噬中的潜力来填补现有研究中的空白,从而可以对乳腺癌的转化进行逆向调节。在我们的研究中,印苦楝素显著抑制了 MDA-MB-231 和 MCF-7 细胞的增殖,其 IC 值分别为 1.97±0.24 和 5.04±0.25 μM。印苦楝素通过减少 Bcl-2 同时诱导 Bax 和半胱天冬酶蛋白表达,并调节 HDAC-2 和 H3K27Ac 表达,显著阻止了细胞周期进程和细胞存活,导致线粒体膜电位丧失。因此,通过吖啶橙、单丹磺酰尸胺(MDC)和 Lysotracker Red 染色观察到特征性自噬溶酶体积累。此外,印苦楝素通过增加 Beclin 1 和 LC3B 并降低 p62 和 mTOR 蛋白表达来诱导自噬信号。因此,我们的研究结果表明,印苦楝素通过表观遗传修饰诱导乳腺癌中的自噬介导的细胞凋亡。