Saeed Mohd, Alshagdali Khalid, Moholkar Disha N, Kandimalla Raghuram, Adnan Kausar Mohd, Aqil Farrukh
Department of Biology, College of Sciences, University of Hail, Hail, Saudi Arabia.
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hail, Hail, Saudi Arabia.
Biomol Biomed. 2024 Nov 5. doi: 10.17305/bb.2024.11267.
Cancer remains a leading cause of mortality, with non-small cell lung cancer (NSCLC) being a primary contributor to cancer-related deaths. Traditional treatment strategies such as chemotherapy, radiation, and hormone therapy often present challenges, including severe side effects, drug resistance, and toxicity. Recent advancements in nanotechnology aim to enhance the effectiveness of cancer therapies by targeting drugs selectively and specifically to tumor cells. Among these innovations, exosomes, or small extracellular vesicles (sEVs), have emerged as promising carriers for drug delivery due to their natural origin and ability to encapsulate both small molecules and biologics. This study explores the use of exosomes derived from camel milk in Hail, Saudi Arabia, as a vehicle for delivering curcumin (CUR), a polyphenol with known chemopreventive properties but limited bioavailability. Camel milk was processed to isolate exosomes through differential centrifugation, followed by characterization using dynamic light scattering, zeta potential measurements, and Western blot analysis to confirm exosomal markers. The encapsulation of CUR into camel milk-derived exosomes demonstrated a 20% loading efficiency as analyzed by UPLC. In vitro antiproliferative assays revealed that the exosomal formulation of CUR (ExoCUR) significantly enhanced cytotoxicity against drug-sensitive (A549) and taxol-resistant (A549TR) lung cancer cells compared to free CUR. Molecular docking studies and molecular dynamics simulations indicated that CUR has a strong binding affinity for the epidermal growth factor receptor (EGFR), comparable to the established drug gefitinib. Furthermore, CUR effectively downregulated EGFR and STAT3 expression in lung cancer cells, suggesting its potential to disrupt key signaling pathways involved in tumor progression. Our findings highlight the potential of camel milk-derived exosomes as an effective and biocompatible delivery system for CUR, offering a promising strategy to overcome the limitations of current cancer therapies and enhance the therapeutic efficacy of chemopreventive agents.
癌症仍然是主要的死亡原因,非小细胞肺癌(NSCLC)是癌症相关死亡的主要原因之一。化疗、放疗和激素疗法等传统治疗策略常常面临挑战,包括严重的副作用、耐药性和毒性。纳米技术的最新进展旨在通过将药物选择性且特异性地靶向肿瘤细胞来提高癌症治疗的有效性。在这些创新中,外泌体或小细胞外囊泡(sEVs)因其天然来源以及能够封装小分子和生物制剂的能力,已成为有前景的药物递送载体。本研究探索了源自沙特阿拉伯哈伊勒骆驼奶的外泌体作为递送姜黄素(CUR)的载体的用途,姜黄素是一种具有已知化学预防特性但生物利用度有限的多酚。通过差速离心法处理骆驼奶以分离外泌体,随后使用动态光散射、zeta电位测量和蛋白质印迹分析进行表征,以确认外泌体标志物。通过超高效液相色谱(UPLC)分析,姜黄素封装到源自骆驼奶的外泌体中的装载效率为20%。体外抗增殖试验表明,与游离姜黄素相比,姜黄素的外泌体制剂(ExoCUR)对药物敏感(A549)和耐紫杉醇(A549TR)肺癌细胞的细胞毒性显著增强。分子对接研究和分子动力学模拟表明,姜黄素与表皮生长因子受体(EGFR)具有很强的结合亲和力,与已上市的药物吉非替尼相当。此外,姜黄素有效地下调了肺癌细胞中EGFR和STAT3的表达,表明其有可能破坏参与肿瘤进展的关键信号通路。我们的研究结果突出了源自骆驼奶的外泌体作为姜黄素有效且生物相容性递送系统的潜力,为克服当前癌症治疗的局限性和提高化学预防剂的治疗效果提供了一种有前景的策略。