PLIN2 confers gefitinib resistance by inhibiting cell apoptosis via activation of EGFR/AKT/survivin in PC9R cells

PLIN2 confers gefitinib resistance by inhibiting cell apoptosis via activation of EGFR/AKT/survivin in PC9R cells
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PLIN2 通过激活 PC9R 细胞中的 EGFR/AKT/survivin 抑制细胞凋亡,从而赋予吉非替尼耐药性

DOI:
10.18632/oncotarget.24153
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发表时间:
2018-01
期刊:
影响因子:
--
通讯作者:
Jian Zhou
Jian Zhou
中科院分区:
--
文献类型:
--
作者:
Meijia Chang;Jie Hu;Tao Fang;Jing Li;Yuanlin Song;Chunxue Bai;Jian Zhou

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表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI)是治疗EGFR激活突变的晚期非小细胞肺癌(NSCLC)患者的一线药物。然而,TKI耐药性的发展是一个重大的临床挑战。在这里,我们表明,亲脂蛋白/脂肪分化相关蛋白perilipin(PLIN)2在吉非替尼耐药的PC 9 R细胞上调; PLIN 2敲低PC 9 R细胞通过抑制癌细胞凋亡在体外和体内,并通过诱导线粒体功能障碍和caspase激活赋予吉非替尼耐药。PLIN 2还显示激活EGFR/AKT/生存素信号传导,并且在临床样品中的吉非替尼抗性细胞中过表达。这些结果表明,PLIN 2通过抑制细胞凋亡和激活EGFR/AKT/生存素途径在肺癌中赋予吉非替尼抗性,因此是EGFR TKI抗性NSCLC患者的潜在治疗靶标。www.impactjournals.com/oncotarget/ OncotTarget,Advance Publications 2018
Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are the first-line drugs for advanced non-small cell lung cancer (NSCLC) patients with activating EGFR mutations. However, the development of TKI resistance is a major clinical challenge. Here we show that the adipophilin/adipose differentiation-related protein perilipin (PLIN)2 was upregulated in gefitinib-resistant PC9R cells; PLIN2 knockdown in PC9R cells conferred gefitinib resistance by inhibiting cancer cell apoptosis in vitro and in vivo and by inducing mitochondrial dysfunction and caspase activation. PLIN2 was also shown to activate EGFR/AKT/survivin signalling and was overexpressed in gefitinib-resistant cells in clinical samples. These results indicate that PLIN2 confers gefitinib resistance in lung cancer by inhibiting apoptosis and activating the EGFR/AKT/survivin pathway, and is thus a potential therapeutic target in EGFR TKI-resistant NSCLC patients. www.impactjournals.com/oncotarget/ Oncotarget, Advance Publications 2018
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