Vimalkumar Pothiyil S, Sivadas Neethu, Murali Vishnu Priya, Sherin Daisy R, Murali Madhukrishnan, Joseph Anuja Gracy, Radhakrishnan Kokkuvayil Vasu, Maiti Kaustabh Kumar
Chemical Sciences and Technology Division, CSIR-National Institute for Interdisciplinary Science and Technology (CSIR-NIIST) Thiruvananthapuram-695019 India
Academy of Scientific and Innovative Research (AcSIR) Ghaziabad-201002 India.
RSC Med Chem. 2024 Sep 9;15(10):3558-75. doi: 10.1039/d4md00391h.
Lam., commonly known as Malabar nutmeg or false nutmeg, is used in traditional medicine and as a spice. Our exploration focuses on malabaricones, a distinct group of secondary metabolites isolated from the fruit rind of . We investigated the selective cytotoxicity of malabaricones against the triple-negative breast cancer (TNBC) cell line. In particular, malabaricone A (Mal-A) displays heightened toxicity towards TNBC cells (MDA-MB-231), with an IC of 8.81 ± 0.03 μM. fluorimetric assays confirmed the apoptotic capability of Mal-A and its capacity to induce nuclear fragmentation. Additionally, ultrasensitive surface-enhanced Raman spectroscopy confirms DNA fragmentation during cellular apoptosis. Cell cycle analysis indicates arrest during the sub-G phase by downregulating key regulatory proteins involved in cell cycle progression. Increased expression levels of caspase 3, 9, and 8 suggest involvement of both extrinsic and intrinsic apoptotic pathways. Finally, assessment of protein expression patterns within apoptotic pathways reveals upregulation of key apoptotic proteins like Fas/FasL, TNF/TNFR1, and p53, coupled with downregulation of several inhibitors of apoptosis proteins such as XIAP, cIAP-2, and Livin. These findings are further verified with molecular docking. Mal-A reveals a strong affinity towards apoptotic proteins, including TNF, Fas, HTRA, Smac, and XIAP, with docking scores ranging from -5.1 to -7.2 kcal mol. Subsequently, molecular dynamics simulation confirms the binding stability. This conclusive evaluation validates Mal-A as a potent phyto-entity against TNBC. To the best of our knowledge, this study represents the first comprehensive anticancer evaluation of Mal-A in TNBC cells.
拉姆,通常被称为马拉巴尔肉豆蔻或假肉豆蔻,用于传统医学和作为香料。我们的探索集中在马拉巴酮类化合物上,这是从其果皮中分离出的一组独特的次生代谢产物。我们研究了马拉巴酮类化合物对三阴性乳腺癌(TNBC)细胞系的选择性细胞毒性。特别是,马拉巴酮A(Mal-A)对TNBC细胞(MDA-MB-231)显示出更高的毒性,IC50为8.81±0.03μM。荧光测定法证实了Mal-A的凋亡能力及其诱导核碎裂的能力。此外,超灵敏表面增强拉曼光谱证实了细胞凋亡过程中的DNA片段化。细胞周期分析表明,通过下调参与细胞周期进程的关键调节蛋白,在亚G期发生停滞。半胱天冬酶3、9和8表达水平的增加表明外在和内在凋亡途径均参与其中。最后,对凋亡途径内蛋白质表达模式的评估揭示了关键凋亡蛋白如Fas/FasL、TNF/TNFR1和p53的上调,同时下调了几种凋亡抑制蛋白如XIAP、cIAP-2和Livin。这些发现通过分子对接得到进一步验证。Mal-A对包括TNF、Fas、HTRA、Smac和XIAP在内的凋亡蛋白具有很强的亲和力,对接分数范围为-5.1至-7.2 kcal/mol。随后,分子动力学模拟证实了结合稳定性。这一结论性评估验证了Mal-A作为一种针对TNBC的有效植物实体。据我们所知,本研究代表了对Mal-A在TNBC细胞中的首次全面抗癌评估。