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[阿司匹林联合二甲双胍诱导甲状腺癌TPC-1细胞凋亡的机制]

[The mechanism of aspirin combined with metformin induced apoptosis of thyroid cancer TPC-1 cells].

作者信息

Qi L, Ye J W, Xue W H, Tian X, Zhang H J

机构信息

Department of Pharmacy, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

Department of Hepatobiliary and Pancreatic Surgery, the First Affiliated Hospital of Zhengzhou University, Open Laboratory of Key Disciplines of Hepatobiliary and Pancreatic Surgery and Digestive Organ Transplantation in Henan Province, Zhengzhou 450052, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2019 Apr 23;41(4):276-281. doi: 10.3760/cma.j.issn.0253-3766.2019.04.006.

Abstract

To explore the effect of aspirin combined with metformin on the apoptosis of thyroid cancer TPC-1 cells and its mechanism. The proliferation and apoptosis of TPC-1 cells treated with different concentrations of aspirin and metformin were detected using cell count kit-8 (CCK-8) assay and flow cytometry, respectively. Western blot was used to detect the expressions of microtubule-associated protein light chain 3 (LC3), p62 and cysteinyl aspartate specific proteinase 3 (caspase-3) after treatment with aspirin, metformin and 3-Methyladenine (3-MA). The relative cell viability of TPC-1 cells treated with 0.5, 1.0, 2.0, 4.0 mmol/L aspirin for 24 and 48 hours were (85.6±9.1)%, (79.9±8.6)%, (57.0±5.3)%, (55.7±5.4)%; (76.7±2.8)%, (75.4±6.1)%, (46.1±4.1)%, (36.3±3.2)%, respectively. The value of half maximal inhibitory concentration (IC(50)) for 24 and 48 hours were 4.297 mmol/L, 2.133 mmol/L, respectively. The apoptotic rate in the 1 mmol/L aspirin treatment group and negative control group were (29.2±8.5)%, (4.2±2.9)%, respectively (<0.05). Moreover, treatment with metformin increased the protein expression of LC3Ⅱ/Ⅰ ratio, and decreased the expression of p62, while treatment with aspirin decreased the expression of LC3Ⅱ/Ⅰ ratio and increased the expression of p62. The relative cell viability of TPC-1 cells treated with metformin, 3-MA, an autophagy inhibitor, and 3-MA combined with metformin were (73.2±9.2)%, (95.8±3.3)%, (59.9±9.2)%, respectively. The apoptotic rates in these groups were (35.5±1.5)%, (12.3±1.4)%, (49.9±5.4)%, respectively. Compared with the metformin group, the relative cell viability in metformin combined with 3-MA group was significantly lower while the apoptotic rate was higher (<0.05), which indicated that treatment with 3-MA enhanced the metformin-induced apoptosis of TPC-1 cells. The relative cell viability of TPC-1 cells in metformin group, aspirin group, metformin combined with aspirin group were (87.3±11.8)%, (85.7±9.6)%, (72.4±8.8)%, respectively. The apoptotic rates in these groups were (29.7±4.0)%, (30.5±6.5)%, (52.5±4.6)%, respectively. Compared with the metformin or aspirin group, the relative cell viability in metformin combined with aspirin group was significantly lower, while the apoptotic rate was higher (<0.05), which indicated that aspirin enhanced the metformin-induced apoptosis of TPC-1 cells. Our findings indicate that metformin-mediated autophagy plays a protective role in metformin-induced apoptosis and proliferation inhibition. Aspirin enhances the metformin-induced apoptosis of thyroid cancer TPC-1 cells through inhibition of autophagy.

摘要

探讨阿司匹林联合二甲双胍对甲状腺癌TPC-1细胞凋亡的影响及其机制。分别采用细胞计数试剂盒-8(CCK-8)法和流式细胞术检测不同浓度阿司匹林和二甲双胍处理的TPC-1细胞的增殖和凋亡情况。采用蛋白质免疫印迹法检测阿司匹林、二甲双胍和3-甲基腺嘌呤(3-MA)处理后微管相关蛋白轻链3(LC3)、p62和半胱氨酸天冬氨酸特异性蛋白酶3(caspase-3)的表达。0.5、1.0、2.0、4.0 mmol/L阿司匹林处理TPC-1细胞24小时和48小时后的相对细胞活力分别为(85.6±9.1)%、(79.9±8.6)%、(57.0±5.3)%、(55.7±5.4)%;(76.7±2.8)%、(75.4±6.1)%、(46.1±4.1)%、(36.3±3.2)%。24小时和48小时的半数最大抑制浓度(IC50)值分别为4.297 mmol/L、2.133 mmol/L。1 mmol/L阿司匹林处理组和阴性对照组的凋亡率分别为(29.2±8.5)%、(4.2±2.9)%(P<0.05)。此外,二甲双胍处理可增加LC3Ⅱ/Ⅰ比值的蛋白表达,降低p62的表达,而阿司匹林处理则降低LC3Ⅱ/Ⅰ比值的表达,增加p62的表达。二甲双胍、自噬抑制剂3-MA以及3-MA联合二甲双胍处理的TPC-1细胞的相对细胞活力分别为(73.2±9.2)%、(95.8±3.3)%、(59.9±9.2)%。这些组的凋亡率分别为(35.5±1.5)%、(12.3±1.4)%、(49.9±5.4)%。与二甲双胍组相比,3-MA联合二甲双胍组的相对细胞活力显著降低,而凋亡率更高(P<0.05),这表明3-MA处理增强了二甲双胍诱导的TPC-1细胞凋亡。二甲双胍组、阿司匹林组、二甲双胍联合阿司匹林组的TPC-1细胞相对细胞活力分别为(87.3±11.8)%、(85.7±9.6)%、(72.4±8.8)%。这些组的凋亡率分别为(29.7±4.0)%、(30.5±6.5)%、(52.5±4.6)%。与二甲双胍组或阿司匹林组相比,二甲双胍联合阿司匹林组的相对细胞活力显著降低,而凋亡率更高(P<0.05),这表明阿司匹林增强了二甲双胍诱导的TPC-1细胞凋亡。我们的研究结果表明,二甲双胍介导的自噬在二甲双胍诱导的凋亡和增殖抑制中起保护作用。阿司匹林通过抑制自噬增强二甲双胍诱导的甲状腺癌TPC-1细胞凋亡。

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