Importin subunit alpha-2 is identified as a potential biomarker for non-small cell lung cancer by integration of the cancer cell secretome and tissue transcriptome

被引:109
作者
Wang, Chun-I. [6 ]
Wang, Chih-Liang [4 ,5 ]
Wang, Chih-Wei [3 ]
Chen, Chi-De [6 ]
Wu, Chih-Ching [2 ]
Liang, Ying [2 ]
Tsai, Ying-Huang [4 ]
Chang, Yu-Sun [2 ,6 ]
Yu, Jau-Song [1 ,2 ,6 ]
Yu, Chia-Jung [1 ,2 ,6 ]
机构
[1] Chang Gung Univ, Dept Cell & Mol Biol, Tao Yuan, Taiwan
[2] Chang Gung Univ, Chang Gung Mol Med Res Ctr, Tao Yuan, Taiwan
[3] Chang Gung Mem Hosp, Dept Pathol, Tao Yuan, Taiwan
[4] Chang Gung Mem Hosp, Dept Thorac Med, Div Pulm Oncol & Intervent Bronchoscopy, Tao Yuan, Taiwan
[5] Chang Gung Univ, Grad Inst Clin Med Sci, Tao Yuan, Taiwan
[6] Chang Gung Univ, Grad Inst Biomed Sci, Tao Yuan, Taiwan
关键词
Biomarker; Non-small cell lung cancer; KPNA2; Secretome; Transcriptome; TUMOR-MARKERS; PROTEOMICS ANALYSIS; KARYOPHERIN ALPHA-2; PROGNOSTIC MARKER; CONDITIONED MEDIA; PROTEIN; EXPRESSION; KPNA2; OVEREXPRESSION; STATISTICS;
D O I
10.1002/ijc.25568
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The cancer cell secretome may contain potentially useful biomarkers. In this study, we integrated the profiles of secreted proteins in lung cancer cell lines with mRNA expression levels from pulmonary adenocarcinoma tissue, with a view to identify effective biomarkers for non-small cell lung cancer (NSCLC). Among the novel candidates isolated, importin subunit alpha-2 (also known as karyopherin subunit alpha [KPNA]-2), was selected for further validation. Immunohistochemical staining revealed overexpression of KPNA2 in the nuclei of tumor cells, compared with adjacent normal cells. A sandwich ELISA assay developed to detect KPNA2 levels in serum samples showed significantly higher serum KPNA2 in NSCLC patients than in healthy controls. A combination of serum KPNA2 and carcinoembryonic antigen displayed higher diagnostic capacity than either marker alone. Importantly, protein levels of KPNA2 in pleural effusion from NSCLC patients were also significantly higher than those from non-lung cancer. Moreover, knockdown of KPNA2 inhibited the migration ability and viability of lung cancer cells. Our results collectively suggest that integration of the cancer cell secretome and transcriptome datasets provides an efficient means of identifying novel biomarkers for NSCLC, such as KPNA2.
引用
收藏
页码:2364 / 2372
页数:9
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