Literature DB >> 26298006

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

Chi-Chen Lin1, Jing-Ting Chen2, Meng-Wei Lin3, Chia-Hao Chan4, Yueh-Feng Wen5, Shin-Bei Wu6, Ting-Wen Chung2, Kevin W Lyu7, Hsiu-Chuan Chou8, Hong-Lin Chan9.   

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.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  DIGE; Gefitinib; Lung adenocarcinoma; PCNT; Proteomics; Resistance; mPR

Mesh:

Substances:

Year:  2015        PMID: 26298006     DOI: 10.1016/j.taap.2015.08.008

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  3 in total

1.  Whole-exome sequencing identifies key mutated genes in T790M wildtype/cMET-unamplified lung adenocarcinoma with acquired resistance to first-generation EGFR tyrosine kinase inhibitors.

Authors:  Chenguang Li; Hailin Liu; Bin Zhang; Liqun Gong; Yanjun Su; Zhenfa Zhang; Changli Wang
Journal:  J Cancer Res Clin Oncol       Date:  2018-04-03       Impact factor: 4.553

2.  Integrative Analysis of Proteome and Ubiquitylome Reveals Unique Features of Lysosomal and Endocytic Pathways in Gefitinib-Resistant Non-Small Cell Lung Cancer Cells.

Authors:  Wang Li; Heyong Wang; Yan Yang; Tian Zhao; Zhixiong Zhang; Ye Tian; Zhaomie Shi; Xiaojun Peng; Fei Li; Yonghong Feng; Lei Zhang; Gening Jiang; Fan Zhang
Journal:  Proteomics       Date:  2018-07-08       Impact factor: 3.984

3.  Progesterone receptor membrane component 1 leads to erlotinib resistance, initiating crosstalk of Wnt/β-catenin and NF-κB pathways, in lung adenocarcinoma cells.

Authors:  Ying Lin; Kazuma Higashisaka; Takuya Shintani; Ayaka Maki; Sachiyo Hanamuro; Yuya Haga; Shinichiro Maeda; Hirofumi Tsujino; Kazuya Nagano; Yasushi Fujio; Yasuo Tsutsumi
Journal:  Sci Rep       Date:  2020-03-16       Impact factor: 4.379

  3 in total

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