EGFR和mTOR双靶点通过调控mTOR下游蛋白磷酸化抑制三阴性乳腺癌细胞生长

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Jing Ma, Chao Dong, Yan-Zhen Cao, Bin-Lin Ma
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引用次数: 2

摘要

目的:检测三阴性乳腺癌细胞系MDA-MB-468中EGFR和mTOR信号通路的激活情况,探讨表皮生长因子受体抑制剂吉非替尼和雷帕霉素靶蛋白抑制剂依维莫司对三阴性乳腺癌细胞的抑制作用。方法:培养三阴性人乳腺癌MDA-MB-468细胞,分别设置空白对照组、单药EGFR抑制剂吉非替尼组、单药mTOR抑制剂依维莫司组和两种药物联合组,检测单药和联合用药对细胞增殖活性、细胞周期和凋亡的影响,并再次采用Western blot检测单药和联合用药干预后细胞株中EGFR和mTOR信号通路蛋白的表达。结果:三阴性乳腺癌中EGFR和p-mTOR蛋白水平高于非三阴性乳腺癌(ppppp)结论:EGFR和mTOR信号通路在三阴性乳腺癌中可被激活;EGFR抑制剂吉非替尼单用和mTOR抑制剂依维莫司单用均能显著抑制人三阴性乳腺癌MDA-MB-468细胞的增殖。EGFR抑制剂吉非替尼与mTOR抑制剂依维莫司联用可通过减少药物剂量达到与单一药物相似的抗肿瘤效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dual Target of EGFR and mTOR Suppresses Triple-Negative Breast Cancer Cell Growth by Regulating the Phosphorylation of mTOR Downstream Proteins.

Dual Target of EGFR and mTOR Suppresses Triple-Negative Breast Cancer Cell Growth by Regulating the Phosphorylation of mTOR Downstream Proteins.

Dual Target of EGFR and mTOR Suppresses Triple-Negative Breast Cancer Cell Growth by Regulating the Phosphorylation of mTOR Downstream Proteins.

Dual Target of EGFR and mTOR Suppresses Triple-Negative Breast Cancer Cell Growth by Regulating the Phosphorylation of mTOR Downstream Proteins.

Objective: To detect the activation of the EGFR and mTOR signaling pathways in the triple negative breast cancer cell line MDA-MB-468 and investigate the inhibitory effect of gefitinib, an epidermal growth factor receptor inhibitor, and everolimus, a target protein inhibitor of rapamycin, on triple negative breast cancer cells.

Methods: Triple negative human breast cancer MDA-MB-468 cells were cultured and blank control group, single EGFR inhibitor gefitinib group, single mTOR inhibitor everolimus group, and two drug combination group were set up respectively to detect the effects of single and combined drugs on cell proliferation activity, cell cycle and apoptosis, and the expression of EGFR and mTOR signal pathway proteins in cell lines after single and combined drug intervention was detected again by Western blot.

Results: The level of EGFR and p-mTOR protein in triple negative breast cancer was higher than in non triple negative breast cancer (P<0.05). The level of mTOR, S6K1, p-EGFR, p-S6K1 was significantly increased when treated with EGF (0ng/mL, 10ng/mL, 100ng/mL) for 1h, compared to without EGF stimulation (P<0.05). The level of p-EGFR, p-mTOR, p-S6K1 protein increased significantly when the cells were exposed to EGF for 2h, respectively (P<0.05). EGFR inhibitor gefitinib alone and the mTOR inhibitor everolimus alone could significantly inhibit the proliferation of human triple negative breast cancer MDA-MB-468 cells in a dose-dependent manner (P<0.05). The level of p-4EBP1 protein in EGFR and mTOR signal pathway was significantly increased after the intervention of gefitinib alone, everolimus alone, and the combination of two drugs (P<0.05).

Conclusion: EGFR and mTOR signaling pathways can be activated in triple negative breast cancer; Both the EGFR inhibitor gefitinib alone and the mTOR inhibitor everolimus alone can significantly inhibit the proliferation of human triple negative breast cancer MDA-MB-468 cells. The combination of the EGFR inhibitor gefitinib and the mTOR inhibitor everolimus may achieve anti-tumor effect similar to that of single drug by reducing the drug dose.

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CiteScore
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