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过氧化物酶和原肌球蛋白作为肺癌和石棉暴露的血浆生物标志物。

Peroxiredoxins and tropomyosins as plasma biomarkers for lung cancer and asbestos exposure.

机构信息

Department of Pathology, HUSLAB and Helsinki University Hospital, Helsinki and Espoo, P.O. 800, FI-00029 HUS, Finland.

出版信息

Lung Cancer. 2012 Aug;77(2):450-9. doi: 10.1016/j.lungcan.2012.03.024. Epub 2012 Apr 24.

Abstract

The prognosis of lung cancer is poor due to late diagnosis, the lack of established screening programs, and the paucity of early biomarkers for high-risk populations. Plasma proteome analysis was used to identify novel biomarkers for diagnosing lung cancer, and to unravel the mechanisms of underlying pathogenesis. Plasma proteins obtained from asbestos-exposed lung cancer cases detected by CT screening, asbestos-exposed subjects, clinical lung cancer patients, and healthy tobacco smokers, 5-6 cases in each group, were separated by two-dimensional gel electrophoresis, and identified with tandem mass spectrometry (LC-MS/MS). Nine proteins were selected for immunological confirmation in a test or validation set of plasma samples from an additional 49 clinical lung cancer cases, 66 asbestos-exposed patients, and 107 healthy tobacco smokers. Twenty-eight unique proteins were differentially expressed between the four study groups (p<0.05). Peroxiredoxin 1 (PRX1) was detected as a novel plasma marker for lung cancer (p=0.001). We also confirmed the previously found association of serum amyloid A with lung cancer (p<0.001). High plasma levels of tropomyosin 4 (TPM4: p<0.001) and peroxiredoxins 1 and 2 (PRX2: p<0.001) correlated with asbestos exposure or a diagnosis of asbestosis. PRX1 and PRX2 exhibited an inverse correlation with tobacco smoking (p<0.001). Plasma peroxiredoxins 1 and 2, and tropomyosin 4 were shown to associate with asbestos-exposure, and peroxiredoxin 1 with lung cancer. High plasma levels of peroxiredoxin 1 may result from genetic damage caused by reactive oxygen species. This study has identified several biomarkers worthy of further investigation in lung cancer and asbestos-related diseases.

摘要

由于晚期诊断、缺乏既定的筛查计划以及缺乏高危人群的早期生物标志物,肺癌的预后较差。本研究通过血浆蛋白质组分析,旨在寻找用于诊断肺癌的新型生物标志物,并阐明潜在发病机制。收集通过 CT 筛查检测到的、接触石棉的肺癌病例、接触石棉的对照者、临床肺癌患者以及健康吸烟人群的血浆蛋白质(每组 5-6 例),通过二维凝胶电泳进行分离,并采用串联质谱法(LC-MS/MS)进行鉴定。选择 9 种蛋白,在另外 49 例临床肺癌病例、66 例接触石棉的患者以及 107 例健康吸烟人群的血浆样本的测试或验证组中,通过免疫法进行验证。四组研究对象间(p<0.05)有 28 种差异表达蛋白。过氧化物酶 1(PRX1)被检测为肺癌的新型血浆标志物(p=0.001)。我们还证实了先前发现的血清淀粉样蛋白 A 与肺癌的相关性(p<0.001)。高浓度的肌球蛋白轻链 4(TPM4:p<0.001)和过氧化物酶 1 和 2(PRX2:p<0.001)与石棉暴露或石棉沉着病的诊断相关。PRX1 和 PRX2 与吸烟呈负相关(p<0.001)。PRX1、PRX2 和 TPM4 与石棉暴露有关,PRX1 与肺癌有关。高水平的过氧化物酶 1 可能是由于活性氧引起的基因损伤所致。本研究鉴定了几种有价值的生物标志物,值得进一步研究在肺癌和与石棉相关的疾病中的作用。

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