Gupta Sunny, Gupta Shipra, Singh Manju, Patel Ashok Kumar
Kusuma School of Biological Sciences, Indian Institute of Technology, Delhi, New Delhi 110016 India.
All India Institute of Ayurveda Delhi, New Delhi, 110076 India.
3 Biotech. 2025 Jun;15(6):186. doi: 10.1007/s13205-025-04349-8. Epub 2025 May 24.
Plant-derived exosome-like nanoparticles represent a novel class of plant-based therapeutics with potential anti-cancer applications. The present study aims to isolate, characterize, and evaluate the -derived exosome-like nanoparticles (ACENPs) for their cytotoxic and apoptotic effects on breast cancer cells. Nanoparticle tracking analysis (NTA) and transmission electron microscopy (TEM) revealed that ACENPs exhibited a mean hydrodynamic diameter of 122.4 ± 5.0 nm and a particle concentration of 1.58 × 10 particles/mL. Cellular uptake studies confirmed the efficient internalization of ACENPs in MCF-7, MDA-MB-453, and MDA-MB-231 breast cancer cells. Cytotoxicity assay demonstrated a significant reduction in cell viability by 17.6%, 25%, and 35.8% in MCF-7, MDA-MB-231, and MDA-MB-453 breast cancer cells, respectively. Apoptosis induction was validated through AO/EB staining, DAPI nuclear fragmentation assays, annexin V-FITC/PI staining, and Western blot analysis of apoptosis-related proteins. Treatment with ACENPs resulted in an increased Bax/Bcl-2 ratio, indicating apoptotic activation. Metabolomic profiling identified bioactive compounds such as arecoline, trigonelline, asarone, and gingerol, known for their anti-cancer properties. Our study findings highlight that ACENPs could be utilized as a promising therapeutic approach for breast cancer treatment. We propose to conduct future research focusing on in vivo validation and optimizing large-scale production for clinical translation.
The online version contains supplementary material available at 10.1007/s13205-025-04349-8.
植物来源的外泌体样纳米颗粒代表了一类新型的植物基疗法,具有潜在的抗癌应用前景。本研究旨在分离、表征并评估槟榔来源的外泌体样纳米颗粒(ACENPs)对乳腺癌细胞的细胞毒性和凋亡作用。纳米颗粒跟踪分析(NTA)和透射电子显微镜(TEM)显示,ACENPs的平均流体动力学直径为122.4±5.0纳米,颗粒浓度为1.58×10颗粒/毫升。细胞摄取研究证实ACENPs能有效内化于MCF-7、MDA-MB-453和MDA-MB-231乳腺癌细胞中。细胞毒性试验表明,在MCF-7、MDA-MB-231和MDA-MB-453乳腺癌细胞中,细胞活力分别显著降低了17.6%、25%和35.8%。通过AO/EB染色、DAPI核碎裂试验、膜联蛋白V-FITC/PI染色以及凋亡相关蛋白的蛋白质印迹分析验证了凋亡诱导情况。用ACENPs处理导致Bax/Bcl-2比值增加,表明凋亡被激活。代谢组学分析鉴定出了具有抗癌特性的生物活性化合物,如槟榔碱、胡芦巴碱、细辛醚和姜辣素。我们的研究结果表明,ACENPs可作为一种有前景的乳腺癌治疗方法。我们建议未来开展聚焦于体内验证和优化大规模生产以实现临床转化的研究。
在线版本包含可在10.1007/s13205-025-04349-8获取的补充材料。