Circulating Exosomal microRNAs as Biomarkers of Colon Cancer

被引:776
作者
Ogata-Kawata, Hiroko [1 ]
Izumiya, Masashi [3 ]
Kurioka, Daisuke [1 ,4 ]
Honma, Yoshitaka [5 ]
Yamada, Yasuhide [5 ]
Furuta, Koh [6 ]
Gunji, Toshiaki [7 ]
Ohta, Hideki [8 ]
Okamoto, Hiroyuki [8 ]
Sonoda, Hikaru [8 ]
Watanabe, Masatoshi [4 ]
Nakagama, Hitoshi [2 ]
Yokota, Jun [1 ,9 ]
Kohno, Takashi [1 ]
Tsuchiya, Naoto [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Genome Biol, Tokyo 104, Japan
[2] Natl Canc Ctr, Res Inst, Div Canc Dev Syst, Tokyo 104, Japan
[3] Tokyo Univ Hosp, Dept Gastroenterol, Tokyo 113, Japan
[4] Yokohama Natl Univ, Grad Sch Engn, Div Mat & Chem Engn, Med Engn Lab, Yokohama, Kanagawa, Japan
[5] Natl Canc Ctr, Gastrointestinal Oncol Div, Tokyo, Japan
[6] Natl Canc Ctr, Div Clin Labs, Tokyo, Japan
[7] NTT Med Ctr Tokyo, Tokyo, Japan
[8] Shionogi & Co Ltd, Osaka, Japan
[9] Inst Predict & Personalized Med Canc IMPPC, Barcelona, Spain
关键词
PROGNOSTIC BIOMARKER; COLORECTAL-CANCER; PLASMA; DYSREGULATION; SIGNATURES; MARKERS; MIR-221; MIRNAS; GROWTH;
D O I
10.1371/journal.pone.0092921
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Purpose: Exosomal microRNAs (miRNAs) have been attracting major interest as potential diagnostic biomarkers of cancer. The aim of this study was to characterize the miRNA profiles of serum exosomes and to identify those that are altered in colorectal cancer (CRC). To evaluate their use as diagnostic biomarkers, the relationship between specific exosomal miRNA levels and pathological changes of patients, including disease stage and tumor resection, was examined. Experimental Design: Microarray analyses of miRNAs in exosome-enriched fractions of serum samples from 88 primary CRC patients and 11 healthy controls were performed. The expression levels of miRNAs in the culture medium of five colon cancer cell lines were also compared with those in the culture medium of a normal colon-derived cell line. The expression profiles of miRNAs that were differentially expressed between CRC and control sample sets were verified using 29 paired samples from post-tumor resection patients. The sensitivities of selected miRNAs as biomarkers of CRC were evaluated and compared with those of known tumor markers (CA19-9 and CEA) using a receiver operating characteristic analysis. The expression levels of selected miRNAs were also validated by quantitative real-time RT-PCR analyses of an independent set of 13 CRC patients. Results: The serum exosomal levels of seven miRNAs (let-7a, miR-1229, miR-1246, miR-150, miR-21, miR-223, and miR-23a) were significantly higher in primary CRC patients, even those with early stage disease, than in healthy controls, and were significantly down-regulated after surgical resection of tumors. These miRNAs were also secreted at significantly higher levels by colon cancer cell lines than by a normal colon-derived cell line. The high sensitivities of the seven selected exosomal miRNAs were confirmed by a receiver operating characteristic analysis. Conclusion: Exosomal miRNA signatures appear to mirror pathological changes of CRC patients and several miRNAs are promising biomarkers for non-invasive diagnosis of the disease.
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页数:9
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