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首页> 外文期刊>Cancer Management and Research >Anticancer Effects of Antihypertensive L-Type Calcium Channel Blockers on Chemoresistant Lung Cancer Cells via Autophagy and Apoptosis
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Anticancer Effects of Antihypertensive L-Type Calcium Channel Blockers on Chemoresistant Lung Cancer Cells via Autophagy and Apoptosis

机译:抗高血压L型钙通道阻断剂通过自噬和凋亡对化学肺癌细胞的抗高血压钙血管阻断

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Purpose: Hypertension and cancer are frequently found comorbidity occurring in same individual. This study was intended to evaluate the anticancer effects of commonly used antihypertensive medications and chemotherapy on chemoresistant lung cancer cells. Methods: Calcium channel blockers (CCBs), including Verapamil, Diltiazem, and Nifedipine, either alone or combined with docetaxel (DOC) or vincristine (VCR) were used to treat A549 lung adenocarcinoma chemoresistant sublines. Cell viability was determined by MTT assay, and colony formation assay was used to demonstrate the long-term effect of CCBs on proliferation of the sublines. Apoptosis was evaluated by Annexin V assay and autophagy intensity was quantitated from acidic vesicular organelle formation. Pan-caspase inhibitor, shATG5 interference and chloroquine were applied to study the roles of Verapamil on apoptosis and autophagy, with related proteins verified by Western blot analysis. Results: Results show that 10 μM of Verapamil and Diltiazem, but not Nifedipine, differentially induce autophagy in DOC-resistant or VCR-resistant A549 cells, respectively. When CCBs are combined with DOC or VCR to treat the sublines, 10 μM of Verapamil induces autophagy more significantly than Diltiazem and Nifedipine, respectively, in DOC-resistant (54.91± 0.76, 18.03± 0.69, 7.05± 0.30) or VCR-resistant A549 (32.41± 1.04, 21.51± 0.63, 7.14± 0.24) cells. Inhibition of apoptosis by pan-caspase inhibitor partly reduced cell death indicates association of caspase-dependent cell death but with persistence of autophagy. Inhibition of autophagy by interfering ATG5 expression reduced c-PARP level and apoptotic cells suggest a pro-death role of autophagy. Chloroquine treatment enhanced autophagosome accumulation and cell death but with reduced c-PARP level suggests that mechanism of caspase-independent cell death also contributes to Verapamil/chemotherapy-induced anticancer effects. Conclusion: Verapamil combined with DOC or VCR induces chemoresistant lung cancer cells to death through autophagy burst and apoptosis more strongly than Diltiazem and Nifedipine. Administering Verapamil or Diltiazem individually with chemotherapy, but not Nifedipine, can be considered in lung cancer patients with hypertension.
机译:目的:高血压和癌症经常发现同一个体的合并症。本研究旨在评估常用的抗高血压药物和化疗对化学肺癌细胞的抗癌效果。方法:钙通道阻滞剂(CCBS),包括维拉帕米,Diltiazem和NifeDipine,单独或与多西紫杉醇(Doc)或vincristine(VCR)组合用于治疗A549肺腺癌化学血管瘤。通过MTT测定法测定细胞活力,并使用菌落形成测定来证明CCBS对寄生对汇流量增殖的长期影响。通过膜蛋白V测定法评估细胞凋亡,并从酸性脉冲细胞器形成中量化自噬强度。应用泛胱天蛋白酶抑制剂,Shatg5干扰和氯喹,用于研究Verapamil对凋亡和自噬的作用,用Western印迹分析验证的相关蛋白质。结果:结果表明,10μm的维拉帕米和Diltiazem,但不是硝苯地平,分别差异地诱导Doc抗性或VCR抗性A549细胞的自噬。当CCBS与DOC或VCR结合以治疗载体时,10μm的维拉帕米分别在DILTIAZEM和NifeDipine中更显着,在DOC抗性中更显着(54.91±0.76,18.03±0.69,7.05±0.30)或VCR抗性A549 (32.41±1.04,21.51±0.63,7.14±0.24)细胞。 PAN-Caspase抑制剂对细胞凋亡的抑制部分降低了细胞死亡表明依赖于胱天蛋白酶依赖性细胞死亡的关联,而是持久性的自噬。通过干扰ATG5表达降低C-PARP水平和凋亡细胞抑制自噬作用表明自噬的死亡作用。氯喹治疗增强自噬体积聚和细胞死亡,但随着C-PARP水平的降低表明,Caspase无关的细胞死亡机制也有助于维拉帕米/化疗诱导的抗癌效果。结论:维拉帕米与DOC或VCR联合诱导Chemolateistant肺癌细胞通过自噬爆发和细胞凋亡比Diltiazem和Nifedipine更强烈。在肺癌患者高血压患者中可以考虑单独使用化疗进行韦拉帕米尔或达尔替米佐姆,但不是硝苯地平。

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