Prognostic biomarker discovery based on proteome landscape of Chinese lung adenocarcinoma

被引:0
|
作者
Huang, Yuqi [1 ,2 ]
Ma, Sheng [3 ]
Xu, Jun-Yu [1 ,5 ]
Qian, Kun [4 ]
Wang, Yaru [3 ]
Zhang, Yi [4 ]
Tan, Minjia [1 ,2 ,5 ]
Xiao, Ting [3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Clin Res Ctr Canc, State Key Lab Mol Oncol,Dept Etiol & Carcinogenesi, Beijing 100021, Peoples R China
[4] Capital Med Univ, Xuanwu Hosp, Dept Thorac Surg, Beijing 100053, Peoples R China
[5] Chinese Acad Sci, Zhongshan Inst Drug Discovery, Shanghai Inst Mat Med, Zhongshan 528400, Guangdong, Peoples R China
关键词
Lung adenocarcinoma; Proteome; Benign lung disease cases; Solid pathological subtype; Prognostic biomarker; MIGRATION INHIBITORY FACTOR; RESPIRATORY SOCIETY CLASSIFICATION; INTERNATIONAL ASSOCIATION; CANCER STATISTICS; SERUM; MITOCHONDRIA; CELLS; TFEB; EXPRESSION; MANAGEMENT;
D O I
10.1186/s12014-023-09449-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Despite recent innovations in imaging and genomic screening promotes advance in diagnosis and treatment of lung adenocarcinoma (LUAD), there remains high mortality of LUAD and insufficient understanding of LUAD biology. Our previous study performed an integrative multi-omic analysis of LUAD, filling the gap between genomic alterations and their biological proteome effects. However, more detailed molecular characterization and biomarker resources at proteome level still need to be uncovered. In this study, a quantitative proteomic experiment of patient-derived benign lung disease samples was carried out. After that, we integrated the proteomic data with previous dataset of 103 paired LUAD samples. We depicted the proteomic differences between non-cancerous and tumor samples and among diverse pathological subtypes. We also found that up-regulated mitophagy was a significant characteristic of early-stage LUAD. Additionally, our integrative analysis filtered out 75 potential prognostic biomarkers and validated two of them in an independent LUAD serum cohort. This study provided insights for improved understanding proteome abnormalities of LUAD and the novel prognostic biomarker discovery offered an opportunity for LUAD precise management.
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页数:11
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