Identification of exosome protein panels as predictive biomarkers for non-small cell lung cancer

被引:15
作者
Luo, Bin [1 ,2 ]
Que, Zujun [3 ]
Lu, Xinyi [1 ]
Qi, Dan [4 ,5 ,6 ]
Qiao, Zhi [7 ]
Yang, Yun [1 ]
Qian, Fangfang [2 ]
Jiang, Yi [2 ]
Li, Yan [1 ]
Ke, Ronghu [4 ,5 ]
Shen, Xiaoyun [8 ]
Xiao, Hua [7 ]
Li, Hegen [2 ]
Wu, Erxi [4 ,5 ,6 ,9 ,10 ,11 ,12 ]
Tian, Jianhui [1 ,2 ,3 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Shanghai Municipal Hosp Tradit Chinese Med, Clin Oncol Ctr, Shanghai 200071, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Longhua Hosp, Dept Oncol, Shanghai 200032, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Shanghai Municipal Hosp Tradit Chinese Med, Inst Oncol, Shanghai 200071, Peoples R China
[4] Neurosci Inst, Dept Neurosurg, Temple, TX 76502 USA
[5] Baylor Scott & White Hlth, Temple, TX 76502 USA
[6] Baylor Coll Med, Dept Neurosurg, Temple, TX 76508 USA
[7] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, State Key Lab Microbial Metab, Joint Int Res Lab Metab & Dev Sci, Shanghai 200240, Peoples R China
[8] Prism Genom Med, Sugar Land, TX 77478 USA
[9] Texas A&M Univ, Sch Med, College Stn, TX 77843 USA
[10] Texas A&M Univ, Irma Lerma Rangel Sch Pharm, College Stn, TX 77843 USA
[11] LIVESTRONG Canc Inst, Austin, TX 78712 USA
[12] Univ Texas Austin, Dell Med Sch, Dept Oncol, Austin, TX 78712 USA
关键词
Exosomes; Proteomics; Biomarkers; Non-small cell lung cancer (NSCLC); Metastasis; EXTRACELLULAR VESICLES; KIDNEY-DISEASE; COMPLEMENT; STATISTICS; MARKERS; MIRNAS; BLOOD; SERUM;
D O I
10.1186/s12575-023-00223-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
BackgroundNon-small cell lung cancer (NSCLC) remains a leading cause of cancer-related deaths worldwide, primarily due to its propensity for metastasis. Patients diagnosed with localized primary cancer have higher survival rates than those with metastasis. Thus, it is imperative to discover biomarkers for the early detection of NSCLC and the timely prediction of tumor metastasis to improve patient outcomes.MethodsHere, we utilized an integrated approach to isolate and characterize plasma exosomes from NSCLC patients as well as healthy individuals. We then conducted proteomics analysis and parallel reaction monitoring to identify and validate the top-ranked proteins of plasma exosomes.ResultsOur study revealed that the proteome in exosomes from NSCLC patients with metastasis was distinctly different from that from healthy individuals. The former had larger diameters and lower concentrations of exosomes than the latter. Furthermore, among the 1220 identified exosomal proteins, we identified two distinct panels of biomarkers. The first panel of biomarkers (FGB, FGG, and VWF) showed potential for early NSCLC diagnosis and demonstrated a direct correlation with the survival duration of NSCLC patients. The second panel of biomarkers (CFHR5, C9, and MBL2) emerged as potential biomarkers for assessing NSCLC metastasis, of which CFHR5 alone was significantly associated with the overall survival of NSCLC patients.ConclusionsThese findings underscore the potential of plasma exosomal biomarkers for early NSCLC diagnosis and metastasis prediction. Notably, CFHR5 stands out as a promising prognostic indicator for NSCLC patients. The clinical utility of exosomal biomarkers offers the potential to enhance the management of NSCLC.
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页数:17
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