Differential mitochondrial proteome analysis of human lung adenocarcinoma and normal bronchial epithelium cell lines using quantitative mass spectrometry. Issue 4 (27th October 2013)

• Record Type: Journal Article
• Authors: Zhang, Wei; Li, Yanting; Yang, Shuanying; Li, Wei; Ming, Zongjuan; Zhang, Yuping; Hou, Yanli; Niu, Zequn; Rong, Biaoxue; Zhang, Xuede; Liu, Xiaoli
• Is Part Of: Thoracic cancer. Volume 4:Issue 4(2013)
• Page Start: 373
• Page End: 379
• Publication Date: 2013-10-27
• Subjects: Adenocarcinoma -- expression -- mitochondrial proteins; Chest -- Cancer -- Periodicals; Chest -- Cancer -- Treatment -- Periodicals; Chest -- Surgery -- Periodicals; 616.99494005
• DOI: 10.1111/1759-7714.12031
• Languages: English
• ISSNs: 1759-7706

Abstract

Abstract: Background: Lung cancer is one of the higher incidences of malignant tumors around the world. At present, tumor markers CEA, CA19‐9, and CA‐125 in serum are used for the diagnosis of lung cancer, however, fewer studies have shown tumor markers for early diagnosis. Therefore, using quantitative mass spectrometry, differential mitochondrial proteome analysis was performed, comparing human lung adenocarcinoma and normal bronchial epithelium cells. Methods: A human lung adenocarcinoma cell line A549 and a normal human bronchial epithelial cell line 16HBE were cultured in vitro . The cell mitochondria of the two cell lines were extracted and purified by differential centrifugation and percoll density gradient centrifugation. The integrity and purity of mitochondria were validated by electron microscopy and Western‐blot. The proteins/peptides from lung cancer cells and normal cells were marked by the same amount of relative and absolute quantification of ectopic tags (iTRAQ). The mixed samples were analyzed and identified by two‐dimensional liquid chromatography – tandem mass spectrometry (2D‐LC‐MS/MS). The proteome was analyzed with different bioinformatic tools. Results: One hundred and sixty‐one mitochondrial proteins were identified. One hundred and fifty‐three mitochondrial proteins, which were expressed differently between 16HBE cells and A549 cells, were identified. Sixty‐seven proteins were high expression, while 86 proteins were lower expression. Expression of three proteins: ornithine aminotransferase (OAT), heat shock protein beta90 (HSP90), and vimentin (VIM), was increased more than twice. Our results, in combination with the literature review, suggest that HSP90 and Vimentin may be the new tumor markers of lung cancer.