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吉非替尼耐药性人肺腺癌中蛋白质表达变化的鉴定:PCNT和mPR在吉非替尼相关耐药性的发展中起关键作用。

Identification of protein expression alterations in gefitinib-resistant human lung adenocarcinoma: PCNT and mPR play key roles in the development of gefitinib-associated resistance.

作者信息

Lin Chi-Chen, Chen Jing-Ting, Lin Meng-Wei, Chan Chia-Hao, Wen Yueh-Feng, Wu Shin-Bei, Chung Ting-Wen, Lyu Kevin W, Chou Hsiu-Chuan, Chan Hong-Lin

机构信息

Institute of Biomedical Science, National Chung-Hsing University, Taichung, Taiwan; Institute of Biomedical Science, and Rong Hsing Research Center for Translational Medicine, National Chung Hsing University, Taiwan; Department of Medical Research and Education, Taichung Veterans General Hospital, Taichung, Taiwan; Division of Chest Medicine, Department of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan.

Department of Medical Science and Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, Taiwan.

出版信息

Toxicol Appl Pharmacol. 2015 Nov 1;288(3):359-73. doi: 10.1016/j.taap.2015.08.008. Epub 2015 Aug 20.

Abstract

Gefitinib is the first-line chemotherapeutic drug for treating non-small cell lung cancer (NSCLC), which comprises nearly 85% of all lung cancer cases worldwide. However, most patients eventually develop drug resistance after 12-18 months of treatment. Hence, investigating the drug resistance mechanism and resistance-associated biomarkers is necessary. Two lung adenocarcinoma cell lines, PC9 and gefitinib-resistant PC9/Gef, were established for examining resistance mechanisms and identifying potential therapeutic targets. Two-dimensional differential gel electrophoresis and matrix-assisted laser desorption ionization time-of-flight mass spectrometry were used for examining global protein expression changes between PC9 and PC9/Gef. The results revealed that 164 identified proteins were associated with the formation of gefitinib resistance in PC9 cells. Additional studies using RNA interference showed that progesterone receptor membrane component 1 and pericentrin proteins have major roles in gefitinib resistance. In conclusion, the proteomic approach enabled identifying of numerous proteins involved in gefitinib resistance. The results provide useful diagnostic markers and therapeutic candidates for treating gefitinib-resistant NSCLC.

摘要

吉非替尼是治疗非小细胞肺癌(NSCLC)的一线化疗药物,NSCLC占全球所有肺癌病例的近85%。然而,大多数患者在接受12至18个月的治疗后最终会产生耐药性。因此,研究耐药机制和耐药相关生物标志物是必要的。建立了两种肺腺癌细胞系,PC9和吉非替尼耐药的PC9/Gef,用于研究耐药机制和鉴定潜在的治疗靶点。采用二维差异凝胶电泳和基质辅助激光解吸电离飞行时间质谱法检测PC9和PC9/Gef之间的整体蛋白质表达变化。结果显示,164种已鉴定的蛋白质与PC9细胞中吉非替尼耐药性的形成有关。使用RNA干扰的进一步研究表明,孕激素受体膜成分1和中心体周围蛋白在吉非替尼耐药中起主要作用。总之,蛋白质组学方法能够鉴定出许多与吉非替尼耐药相关的蛋白质。这些结果为治疗吉非替尼耐药的NSCLC提供了有用的诊断标志物和治疗候选物。

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