Fengping Wang, Jun Liu, Wenliang Liao, Lixiang Zheng, Shuai Qian, Lisi Mao
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Additionally, animal model experiments were conducted to validate the therapeutic potential of Matrine alkaloids in NSCLC treatment.</p><p><strong>Results: </strong>Our findings demonstrate that Matrine alkaloids disrupt DNA damage repair processes in NSCLC cells, leading to increased sensitivity to chemotherapy. Molecular docking studies revealed the intricate mechanisms by which Matrine alkaloids interact with DNA repair proteins, impacting cell survival and proliferation. Both cell experiments and animal models confirmed the chemosensitizing effects of Matrine alkaloids in NSCLC treatment.</p><p><strong>Conclusion: </strong>Matrine alkaloids offer a promising avenue for overcoming chemotherapy resistance in NSCLC by interfering with DNA repair pathways. 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引用次数: 0
摘要
背景:非小细胞肺癌(NSCLC非小细胞肺癌(NSCLC)因其高发病率和对化疗的耐药性而成为医学领域的一大挑战。非小细胞肺癌的化疗耐药性会降低治疗效果,导致患者预后不佳。马钱子碱通过靶向DNA修复机制,有望逆转NSCLC的化疗耐药性:利用分子动力学模拟,我们探索了马钱子碱与DNA修复相关蛋白之间的相互作用,以阐明它们对NSCLC细胞的影响。体外实验包括用Matrine生物碱处理A549/DDP细胞,以评估其对肺癌细胞的增敏作用。此外,还进行了动物模型实验,以验证松脂酸生物碱在治疗 NSCLC 方面的治疗潜力:结果:我们的研究结果表明,Matrine 生物碱能破坏 NSCLC 细胞的 DNA 损伤修复过程,从而提高细胞对化疗的敏感性。分子对接研究揭示了Matrine生物碱与DNA修复蛋白相互作用、影响细胞存活和增殖的复杂机制。细胞实验和动物模型都证实了马钱子碱在 NSCLC 治疗中的化疗增敏作用:结论:马钱子碱通过干扰DNA修复途径,为克服NSCLC的化疗耐药性提供了一条很有前景的途径。这项研究为今后的临床研究奠定了坚实的基础,以探究Matrine生物碱作为有效治疗剂提高NSCLC治疗效果的潜力。
Matrine alkaloids modulating DNA damage repair in chemoresistant non-small cell lung cancer cells.
Background: Non-small cell lung cancer (NSCLC) presents a significant challenge in the medical field due to its high incidence and resistance to chemotherapy. Chemoresistance in NSCLC diminishes treatment efficacy and contributes to poor patient outcomes. Matrine alkaloids have shown promise in reversing chemotherapy resistance in NSCLC by targeting DNA repair mechanisms.
Methods: Utilizing molecular dynamics simulations, we explored the interactions between Matrine alkaloids and DNA repair-related proteins to elucidate their impact on NSCLC cells. In vitro experiments involved treating A549/DDP cells with Matrine alkaloids to evaluate their sensitizing effects on lung cancer cells. Additionally, animal model experiments were conducted to validate the therapeutic potential of Matrine alkaloids in NSCLC treatment.
Results: Our findings demonstrate that Matrine alkaloids disrupt DNA damage repair processes in NSCLC cells, leading to increased sensitivity to chemotherapy. Molecular docking studies revealed the intricate mechanisms by which Matrine alkaloids interact with DNA repair proteins, impacting cell survival and proliferation. Both cell experiments and animal models confirmed the chemosensitizing effects of Matrine alkaloids in NSCLC treatment.
Conclusion: Matrine alkaloids offer a promising avenue for overcoming chemotherapy resistance in NSCLC by interfering with DNA repair pathways. This study lays a solid foundation for future clinical investigations into the potential of Matrine alkaloids as effective therapeutic agents for enhancing NSCLC treatment outcomes.
期刊介绍:
BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.