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    請使用永久網址來引用或連結此文件: https://ir.lib.ncu.edu.tw/handle/987654321/105823


    題名: Qualification and Verification of Serological Biomarker Candidates for Lung Adenocarcinoma by Targeted Mass Spectrometry
    作者: 吳忻怡;Wu, Hsin-Yi;Goan, Yih-Gang;Chang, Ying-Hua;Yang, Yi-Fang;Chang, Hsiao-Jen;Cheng, Pin-Nan;Wu, Chih-Chieh;Zgoda, Victor G;Chen, Yu-Ju;Liao, Pao-Chi
    貢獻者: 總教學中心通識教育中心
    關鍵詞: adenocarcinoma;Adenocarcinoma - blood;Adenocarcinoma - diagnosis;Adenocarcinoma - metabolism;Aged;Aged, 80 and over;Amino Acid Sequence;biomarkers;Biomarkers, Tumor - blood;Biomarkers, Tumor - metabolism;Blood Proteins - analysis;Blood Proteins - metabolism;Female;Humans;lung neoplasms;Lung Neoplasms - blood;Lung Neoplasms - diagnosis;Lung Neoplasms - metabolism;lungs;Male;mass spectrometry;Mass Spectrometry - methods;Middle Aged;Molecular Sequence Data;mortality;Neoplasm Staging;patients;peptides;Peptides - blood;Peptides - metabolism;proteins;proteome;Proteomics - methods;Reproducibility of Results;Sensitivity and Specificity;therapeutics
    日期: 2015-01-01
    上傳時間: 2026-04-23 12:55:17 (UTC+8)
    出版者: American Chemical Society;United States: American Chemical Society
    摘要: 摘要: Lung cancer is the leading cause of cancer mortality worldwide. Although many biomarkers have been identified for lung cancer, their low specificity and sensitivity present an urgent need for the identification of more candidate biomarkers. In this study, we conducted MRM-based targeted analysis to evaluate the potential utility of a list of candidate proteins for lung cancer diagnosis. A total of 1249 transitions of 420 peptides representing 102 candidate proteins from our previous study and the literature were first screened by MRM analysis in pooled plasma samples, resulting in 78 proteins remaining in the list. Relative quantification of these 78 proteins was further performed in 60 individual plasma samples from lung adenocarcinoma patients in stages I–III and matched healthy control subjects. Ultimately, nine proteins were found to be able to distinguish patients from controls. Further combinations of five, three, and two candidate marker proteins improved the sensitivity to discriminate patients from controls and resulted in a merged AUC value of nearly 1.00 in stages I–III patients versus controls. Our results highlighted several possible markers for lung adenocarcinoma, and the proposed protein panels require further validation in a larger cohort to evaluate their potential use in clinical applications or development of therapeutics.
    其他題名: J. Proteome Res
    出版者: United States: American Chemical Society
    出版日期: 2015-08-07
    出處: Journal of proteome research, 2015-08, Vol.14 (8), p.3039-3050
    資源來源: American Chemical Society Journals
    版權: Copyright © American Chemical Society
    識別號: ISSN: 1535-3893
    識別號: ISSN: 1535-3907
    識別號: EISSN: 1535-3907
    識別號: DOI: 10.1021/pr501195t
    識別號: PMID: 26120931
    顯示於類別:[通識教育中心] 期刊論文

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