Literature DB >> 25054025

Transthyretin as a potential biomarker for the differential diagnosis between lung cancer and lung infection.

Hongmei Ding1, Jianhua Liu2, Rong Xue3, Peng Zhao3, Yi Qin4, Fang Zheng4, Xuguo Sun4.   

Abstract

Satisfactory biomarkers for screening and early diagnosis of lung cancer remain scarce and require further investigation. The aim of the present study was to examine the changes of the biochemical and protein composition in the serum and pleural effusion from lung cancer and lung infection (bacterial pneumonia) patients. A total of 92 patients with lung cancer, 38 with bacterial pneumonia and 42 healthy controls were enrolled in the study. The serum levels of cholesterol, apolipoprotein A and transthyretin (TTR) in the lung cancer patients were higher than that of the lung infection patients (P<0.05). The levels of TTR were higher, whereas the activity of adenosine deaminase (ADA) was lower in the pleural effusion from the lung cancer patients compared to the lung infection patients (P<0.05). Furthermore, the pleural effusion/serum TTR ratios in the lung cancer patients were higher, whereas the ratios of ADA were lower (P<0.05). By matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analysis, four major peaks corresponding to native TTR, Sul-TTR, Cys-TTR and Cysgly-TTR were observed in the serum of the lung cancer and lung infection patients. A significant increase was found in the proportion of Cysgly-TTR in the pleural effusion from the patients with lung cancer. The data indicated that a combination of pleural effusion/serum TTR ratios and modified TTR may be beneficial for the differential diagnosis between lung cancer and lung infection.

Entities:  

Keywords:  lung cancer; lung infection; matrix-assisted laser desorption/ionization time-of-flight mass spectrometry; pleural effusion; transthyretin

Year:  2014        PMID: 25054025      PMCID: PMC4106510          DOI: 10.3892/br.2014.313

Source DB:  PubMed          Journal:  Biomed Rep        ISSN: 2049-9434


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