Li Juan, Zheng Lei, Yan Mi, Wu Jing, Liu Yongqing, Tian Xiaona, Jiang Wen, Zhang Lu, Wang Rongmei
Department of Clinical Pharmacy, The Second Hospital of Shandong University, Jinan, Shandong 250033, P.R. China.
Department of Pharmacy, Shandong Provincial Third Hospital, Jinan, Shandong 250031, P.R. China.
Oncol Lett. 2020 Jan;19(1):379-387. doi: 10.3892/ol.2019.11069. Epub 2019 Nov 8.
Lung cancer is one of the most common cancers, which is the leading cause of cancer-related death among various cancers worldwide. Flavokawain A (FKA), a chalcone found in the kava plant, exerts potent anticancer activity. However, the activity and mechanisms of FKA in inhibiting the viability of paclitaxel (PTX)-resistant lung cancer A549 (A549/T) have not been investigated. In the present study, the effect of FKA on the viability of A549/T and hepatotoxicity in normal liver epithelial cells was detected by Cell Counting Kit-8 assay. Flow cytometry, western blot analysis and Annexin V-FITC/PI apoptosis detection kit were used to assess cell apoptosis. The effect of FKA on permeability-glycoprotein (P-gp) expression was measured by reverse transcription-PCR and western blot analysis. The results indicated that FKA dose-dependently inhibited cell proliferation and induced cell apoptosis in PTX-resistant A549/T cells, with an IC value of ~21 µM, while the IC value of A549/T cells to PTX was 34.64 µM. FKA had no hepatic toxicity in liver epithelial cells. P-gp, which contributes to the chemoresistant phenotype, was not expressed in A549 cells but was remarkably enhanced in A549/T cells. FKA (30 µM) decreased P-gp protein expression at 24 h by 3-fold. Furthermore, FKA downregulated P-gp expression by blocking the PI3K/Akt pathway. These findings suggest FKA as a potential candidate for the treatment of PTX-resistant lung cancer.
肺癌是最常见的癌症之一,是全球各种癌症中癌症相关死亡的主要原因。黄烷卡瓦因A(FKA)是一种在卡瓦植物中发现的查耳酮,具有强大的抗癌活性。然而,FKA抑制耐紫杉醇(PTX)的肺癌A549(A549/T)细胞活力的活性和机制尚未得到研究。在本研究中,通过细胞计数试剂盒-8检测法检测了FKA对A549/T细胞活力以及对正常肝上皮细胞肝毒性的影响。采用流式细胞术、蛋白质免疫印迹分析和膜联蛋白V-FITC/PI凋亡检测试剂盒评估细胞凋亡。通过逆转录聚合酶链反应和蛋白质免疫印迹分析测定FKA对通透性糖蛋白(P-gp)表达的影响。结果表明,FKA剂量依赖性地抑制耐PTX的A549/T细胞的增殖并诱导细胞凋亡,IC值约为21μM,而A549/T细胞对PTX的IC值为34.64μM。FKA对肝上皮细胞无肝毒性。导致化疗耐药表型的P-gp在A549细胞中不表达,但在A549/T细胞中显著增强。FKA(30μM)在24小时时使P-gp蛋白表达降低了3倍。此外,FKA通过阻断PI3K/Akt信号通路下调P-gp表达。这些发现表明FKA是治疗耐PTX肺癌的潜在候选药物。