Liquid Biopsy for Pancreatic Cancer by Serum Extracellular Vesicle-Encapsulated Long Noncoding RNA HEVEPA

被引:1
作者
Takahashi, Kenji [1 ,7 ]
Inuzuka, Tatsutoshi [2 ]
Shimizu, Yuta [2 ]
Sawamoto, Kazuki [1 ]
Taniue, Kenzui [1 ,3 ]
Ono, Yusuke [4 ]
Asai, Fumi [2 ]
Koyama, Kazuya [1 ]
Sato, Hiroki [1 ]
Kawabata, Hidemasa [1 ]
Iwamoto, Hidetaka [1 ]
Yamakita, Keisuke [1 ]
Kitano, Yohei [1 ]
Teramoto, Takashi [5 ]
Fujiya, Mikihiro [1 ]
Fujii, Satoshi [6 ]
Mizukami, Yusuke [1 ]
Okumura, Toshikatsu [1 ]
机构
[1] Asahikawa Med Univ, Dept Med, Div Gastroenterol, Asahikawa, Hokkaido, Japan
[2] HU Gp Res Inst GK, Akiruno, Japan
[3] Univ Tokyo, Isotope Sci Ctr, Bunkyo Ku, Tokyo, Japan
[4] Sapporo Higashi Tokushukai Hosp, Inst Biomed Res, Sapporo, Japan
[5] Asahikawa Med Univ, Div Math, Asahikawa, Hokkaido, Japan
[6] Asahikawa Med Univ, Dept Lab Med, Asahikawa, Hokkaido, Japan
[7] Asahikawa Med Univ, 2 1 1 1,Midorigaoka Higashi, Asahikawa, Hokkaido 0788510, Japan
关键词
long noncoding RNA; extracellular vesicles; exosome; liquid biopsy; pancreatic ductal adenocarcinoma; EXOSOMES;
D O I
10.1097/MPA.0000000000002315
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: The role of long noncoding RNAs (lncRNAs) in pancreatic ductal adenocarcinoma (PDAC) remain unclear. Extracellular vesicle (EV)-encapsulated RNAs could be effective targets for liquid biopsy. We aimed to identify previously unknown EV-encapsulated lncRNAs in PDAC and establish highly accurate methods for isolating EVs. Materials and Methods: Extracellular vesicles were isolated using existing and newly developed methods, namely, PEViA-UC and PEViA-IP, from serum samples of 20 patients with PDAC, 22 patients with intraductal papillary mucinous neoplasms, and 21 healthy individuals. Extracellular vesicle lncRNA expression was analyzed using digital PCR. Results: Gene expression analysis using cDNA microarray revealed a highly expressed lncRNA, HEVEPA, in serum EVs from patients with PDAC. We established PEViA-UC and PEViA-IP using PEViA reagent, ultracentrifugation, and immunoprecipitation. Although detection of EV-encapsulated HEVEPA using existing methods is challenging, PEViA-UC and PEViA-IP detected EV HEVEPA, which was highly expressed in patients with PDAC compared with non-PDAC patients. The detection sensitivity for discriminating PDAC from non-PDAC using the combination of HEVEPA and HULC, which are highly expressed lncRNAs in PDAC, and carbohydrate antigen 19-9 (CA19-9), was higher than that of HEVEPA, HULC, or CA19-9 alone. Conclusions: Extracellular vesicle lncRNAs isolated using PEViA-IP and CA19-9 together could be effective targets in liquid biopsy for PDAC diagnosis.
引用
收藏
页码:e395 / e404
页数:10
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