Kundu Sweta, Saha Suvodeep, Ghosh Suparna, Sarkar Sampriti, Kotal Atanu, Acharya Chowdhury Avik
Department of Biosciences, JIS University, 81, Nilgunj Road, Agarpara, Kolkata, West Bengal, 700109, India.
Applied Biodiversity Lab, Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India.
Arch Pharm Res. 2025 Sep 9. doi: 10.1007/s12272-025-01565-x.
Bacoside A (BCA), a triterpenoid saponin isolated from Bacopa monnieri, exhibits diverse pharmacological properties, including neuroprotective, hepatoprotective, anti-stress, anti-inflammatory, and anti-ulcer effects. In the present study, BCA demonstrates pronounced anticancer activity against K562 chronic myelogenous leukemia (CML) cells by modulating autophagy-apoptosis dynamics. BCA induces dose- and time-dependent cytotoxicity in K562 cells while sparing normal human peripheral blood mononuclear cells (hPBMCs) and Vero cells, indicating therapeutic selectivity. Mechanistically, BCA elicits a biphasic cellular response characterized by autophagy induction at 24 h, followed by caspase-dependent apoptosis at 48 h. Autophagy activation was confirmed by the formation of Monodansylcadaverine-positive autophagic vacuoles, upregulation of Beclin-1 and LC3-II, and increased LC3 puncta in EGFP-LC3-transfected K562 cells. Notably, BCA treatment led to persistent accumulation of p62/SQSTM1 despite functional autophagic flux. Co-immunoprecipitation analysis revealed p62/SQSTM1-LC3-II interactions, while siRNA-mediated silencing of p62/SQSTM1 attenuated LC3-II accumulation, implicating p62/SQSTM1 as a positive modulator of autophagy. Moreover, p62/SQSTM1 facilitated apoptosis progression by interacting with and activating caspase-8, thereby bridging autophagy and apoptosis. Pharmacological inhibition of autophagy using 3-methyladenine abrogated both autophagic and apoptotic responses, establishing autophagy as a prerequisite for BCA-induced cell death. BCA promoted ERK1/2 activation and concomitant suppression of mTOR pathway via dephosphorylation of mTOR and 4E-BP1. Inhibition of ERK1/2 using PD98059 reversed mTOR dephosphorylation and autophagy induction, whereas mTOR overexpression restored ERK1/2 phosphorylation to basal levels. Collectively, these findings delineate BCA as a novel autophagy-inducing agent in CML, exerting cytotoxic effects via ERK1/2-mTOR signaling and p62/SQSTM1-mediated autophagy-apoptosis crosstalk.
胡黄连苷A(BCA)是从假马齿苋中分离出的一种三萜皂苷,具有多种药理特性,包括神经保护、肝脏保护、抗应激、抗炎和抗溃疡作用。在本研究中,BCA通过调节自噬-凋亡动态对K562慢性粒细胞白血病(CML)细胞表现出显著的抗癌活性。BCA在K562细胞中诱导剂量和时间依赖性细胞毒性,同时对正常人外周血单个核细胞(hPBMCs)和非洲绿猴肾细胞(Vero细胞)无毒性,表明其具有治疗选择性。机制上,BCA引发双相细胞反应,其特征是在24小时诱导自噬,随后在48小时发生半胱天冬酶依赖性凋亡。通过单丹磺酰尸胺阳性自噬泡的形成、Beclin-1和LC3-II的上调以及在EGFP-LC3转染的K{562}细胞中LC3斑点的增加,证实了自噬激活。值得注意的是,尽管自噬通量正常,但BCA处理导致p62/SQSTM1持续积累。免疫共沉淀分析揭示了p62/SQSTM1-LC3-II相互作用,而小干扰RNA介导的p62/SQSTM1沉默减弱了LC3-II积累,这表明p62/SQSTM1是自噬的正向调节剂。此外,p62/SQSTM1通过与半胱天冬酶-8相互作用并激活半胱天冬酶-8促进凋亡进程,从而在自噬和凋亡之间建立联系。使用3-甲基腺嘌呤对自噬进行药理学抑制消除了自噬和凋亡反应,确立了自噬是BCA诱导细胞死亡的先决条件。BCA通过mTOR和4E-BP1的去磷酸化促进ERK1/2激活并同时抑制mTOR通路。使用PD98059抑制ERK {1/2}可逆转mTOR去磷酸化和自噬诱导,而mTOR过表达可将ERK {1/2}磷酸化恢复至基础水平。总的来说,这些发现表明BCA是一种新型的CML自噬诱导剂,通过ERK1/2-mTOR信号传导和p62/SQSTM1介导的自噬-凋亡串扰发挥细胞毒性作用。