Ogata-Kawata Hiroko, Izumiya Masashi, Kurioka Daisuke, Honma Yoshitaka, Yamada Yasuhide, Furuta Koh, Gunji Toshiaki, Ohta Hideki, Okamoto Hiroyuki, Sonoda Hikaru, Watanabe Masatoshi, Nakagama Hitoshi, Yokota Jun, Kohno Takashi, Tsuchiya Naoto
Division of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Department of Gastroenterology, The University of Tokyo Hospital, Tokyo, Japan.
PLoS One. 2014 Apr 4;9(4):e92921. doi: 10.1371/journal.pone.0092921. eCollection 2014.
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.
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.
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.
Exosomal miRNA signatures appear to mirror pathological changes of CRC patients and several miRNAs are promising biomarkers for non-invasive diagnosis of the disease.
外泌体微小RNA(miRNA)作为癌症潜在的诊断生物标志物备受关注。本研究旨在表征血清外泌体的miRNA谱,并鉴定在结直肠癌(CRC)中发生改变的miRNA。为评估其作为诊断生物标志物的用途,研究了特定外泌体miRNA水平与患者病理变化(包括疾病分期和肿瘤切除)之间的关系。
对88例原发性CRC患者和11例健康对照血清样本中富含外泌体的部分进行miRNA微阵列分析。还比较了五种结肠癌细胞系培养基中miRNA的表达水平与正常结肠来源细胞系培养基中的表达水平。使用来自肿瘤切除术后患者的29对样本验证了CRC和对照样本组之间差异表达的miRNA的表达谱。使用受试者工作特征分析评估所选miRNA作为CRC生物标志物的敏感性,并与已知肿瘤标志物(CA19-9和CEA)的敏感性进行比较。还通过对一组独立的13例CRC患者进行定量实时RT-PCR分析来验证所选miRNA的表达水平。
原发性CRC患者,即使是早期疾病患者,血清外泌体中七种miRNA(let-7a、miR-1229、miR-1246、miR-150、miR-21、miR-223和miR-23a)的水平明显高于健康对照,并且在肿瘤手术切除后显著下调。这些miRNA在结肠癌细胞系中的分泌水平也明显高于正常结肠来源的细胞系。通过受试者工作特征分析证实了所选七种外泌体miRNA的高敏感性。
外泌体miRNA特征似乎反映了CRC患者的病理变化,几种miRNA有望成为该疾病非侵入性诊断的生物标志物。