首页> 美国卫生研究院文献>Molecular Medicine Reports >Low-frequency ultrasound and microbubbles combined with simvastatin promote the apoptosis of MCF-7 cells by affecting the LATS1/YAP/RHAMM pathway
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Low-frequency ultrasound and microbubbles combined with simvastatin promote the apoptosis of MCF-7 cells by affecting the LATS1/YAP/RHAMM pathway

机译:低频超声和微泡联合辛伐他汀通过影响LATS1 / YAP / RHAMM途径促进MCF-7细胞凋亡

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摘要

Ultrasound scanning has widespread used in clinical practice and also has therapeutic applications. Simvastatin is a statins that is able to competitively inhibit the activity of 3-hydroxy-3-methylglutaryl-coenzyme A reductase. The aim of the present study was to investigate the roles and mechanisms of low-frequency ultrasound (LFU) and microbubbles combined with simvastatin on MCF-7 cell growth and apoptosis. Cell viability, apoptosis and cell cycle were evaluated using an MTT assay and flow cytometry, respectively. The expression of related proteins was measured by western blot assay. The results revealed that simvastatin and LFU with microbubbles reduces the viability of MCF-7 cells. The combination of LFU and microbubbles with simvastatin promoted the apoptosis of MCF-7 cells. Furthermore, it was confirmed that LFU and microbubbles combined with simvastatin affected the large tumor suppressor 1 (LATS1)/yes-associated protein (YAP)/receptor of the hyaluronan-mediated motility (RHAMM) pathway in MCF-7 cells. It was determined that LATS1 acts as a negative regulator in the LATS1/YAP/RHAMM pathway in MCF-7 cells. In conclusion, the results of the present study indicate that LFU and microbubbles combined with simvastatin promotes the apoptosis of MCF-7 cells via the LATS1/YAP/RHAMM pathway. The present study suggested a possible strategy for the treatment of breast cancer.
机译:超声扫描已在临床实践中广泛使用,也具有治疗应用。辛伐他汀是一种他汀类药物,能够竞争性地抑制3-羟基-3-甲基戊二酰辅酶A还原酶的活性。本研究的目的是研究低频超声(LFU)和微泡联合辛伐他汀对MCF-7细胞生长和凋亡的作用和机制。分别使用MTT测定法和流式细胞仪评估细胞活力,凋亡和细胞周期。通过蛋白质印迹法测定相关蛋白的表达。结果显示辛伐他汀和LFU带有微泡会降低MCF-7细胞的活力。 LFU和微泡与辛伐他汀的组合促进了MCF-7细胞的凋亡。此外,已证实LFU和微泡与辛伐他汀联合可影响MCF-7细胞中的大肿瘤抑制因子1(LATS1)/是相关蛋白(YAP)/透明质酸介导的运动性(RHAMM)受体。已确定LATS1在MCF-7细胞的LATS1 / YAP / RHAMM途径中充当负调节剂。总之,本研究的结果表明,LFU和微泡与辛伐他汀联合可通过LATS1 / YAP / RHAMM途径促进MCF-7细胞的凋亡。本研究提出了一种治疗乳腺癌的可能策略。

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