Alpha-2-macroglobulin as a novel diagnostic biomarker for human bladder cancer in urinary extracellular vesicles

被引:11
作者
Lee, Jisu [1 ]
Park, Hyun Sik [2 ]
Han, Seung Ro [1 ,3 ]
Kang, Yun Hee [1 ,3 ]
Mun, Ji Young [4 ]
Shin, Dong Wook [5 ]
Oh, Hyun-Woo [6 ]
Cho, Yoon-Kyoung [7 ,8 ]
Lee, Myung-Shin [1 ,3 ]
Park, Jinsung [9 ]
机构
[1] Eulji Univ Sch Med, Dept Microbiol & Immunol, Daejeon, South Korea
[2] Eulji Univ Hosp, Eulji Univ, Sch Med, Dept Urol, Daejeon, South Korea
[3] Eulji Univ, Eulji Biomed Sci Res Inst, Sch Med, Daejeon, South Korea
[4] Korea Brain Res Inst, Neural Circuit Res Grp, Daegu, South Korea
[5] Sungkyunkwan Univ, Support Care Ctr, Samsung Med Ctr, Dept Family Med, Seoul, South Korea
[6] Korea Res Inst Biosci & Biotechnol, Core FacilityManagement Ctr, Daejeon, South Korea
[7] Ulsan Natl Inst Scienceand Technol UNIST, Dept Biomed Engn, Ulsan, South Korea
[8] Inst Basic Sci IBS, Ctr Soft & Living Matter, Ulsan, South Korea
[9] Eulji Univ, Uijeongbu Eulji Med Ctr, Dept Urol, Uijeongbu si, South Korea
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
基金
新加坡国家研究基金会;
关键词
alpha-2-macroglobulin; bladder cancer; extracellular vesicles (EVs); urine; biomarker; EXOSOMES; IDENTIFICATION; CYSTOSCOPY; MECHANISMS; PROSTATE; CELLS;
D O I
10.3389/fonc.2022.976407
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Extracellular vesicles (EVs) derived from urine are promising tools for the diagnosis of urogenital cancers. Urinary EVs (uEVs) are considered potential biomarkers for bladder cancer (BC) because urine is in direct contact with the BC tumor microenvironment and thus reflects the current state of the disease. However, challenges associated with the effective isolation and analysis of uEVs complicate the clinical detection of uEV-associated protein biomarkers. Herein, we identified uEV-derived alpha-2-macroglobulin (a2M) as a novel diagnostic biomarker for BC through comparative analysis of uEVs obtained from patients with BC pre- and post-operation using an antibody array. Furthermore, enzyme-linked immunosorbent assay of uEVs isolated from patients with BC (n=60) and non-cancer control subjects (n=23) validated the significant upregulation of a2M expression in patient uEVs (p<0.0001). There was no significant difference in whole urine a2M levels between patients with BC and controls (p=0.317). We observed that compared to classical differential centrifugation, ExoDisc, a centrifugal microfluidic tangential flow filtration device, was a significantly more effective separation method for uEV protein analysis. We expect that our approach for EV analysis will provide an efficient route for the identification of clinically meaningful uEV-based biomarkers for cancer diagnosis.
引用
收藏
页数:13
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