PI3K/Akt/mTOR and CDK4 combined inhibition enhanced apoptosis of thyroid cancer cell lines

N. Hamidipour, M. Fazeli, M. Hedayati, M. Dehghani, R. Gerami
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引用次数: 3

Abstract

Introduction Thyroid cancer is a malignant disease with poor prognosis. The PI3K/Akt/mTOR and Cyclin-Dependent Kinase 4 (CDK4) pathways are vital regulators of tumor cell proliferation and survival. Therefore the present study was designed to use dual inhibition of such pathways to kill thyroid cancer cells. Methods and materials The effects of each inhibitors on human ATC and BCPAP cell lines were evaluated by MTT assay. The suitable concentrations of inhibitors were determined and synergistic effects of such inhibitors were evaluated by bax/bcl-2 mRNA ratio, Caspase-3, and Caspase-9 activity assay as well as Akt, mTOR, and CDK4. Results:Our finding showed that both ATC and BCPAP cell proliferation is significantly inhibited by PD-332991(PD) and NVP-BEZ235 (NVP) in a time and concentration-dependent manner (P
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PI3K/Akt/mTOR和CDK4联合抑制可促进甲状腺癌细胞的凋亡
甲状腺癌是一种预后不良的恶性疾病。PI3K/Akt/mTOR和周期蛋白依赖性激酶4 (Cyclin-Dependent Kinase 4, CDK4)通路是肿瘤细胞增殖和存活的重要调控因子。因此,本研究旨在利用这些途径的双重抑制来杀死甲状腺癌细胞。方法与材料采用MTT法评价各抑制剂对人ATC和BCPAP细胞株的影响。通过bax/bcl-2 mRNA比值、Caspase-3、Caspase-9活性测定以及Akt、mTOR、CDK4检测,确定合适的抑制剂浓度,评价抑制剂的协同作用。结果:我们发现PD-332991(PD)和NVP- bez235 (NVP)对ATC和BCPAP细胞的增殖均有明显的抑制作用,并呈时间和浓度依赖性(P
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