Nonaka Ryoji, Nishimura Junichi, Kagawa Yoshinori, Osawa Hideki, Hasegawa Junichi, Murata Kohei, Okamura Shu, Ota Hirofumi, Uemura Mamoru, Hata Taishi, Takemasa Ichiro, Mizushima Tsunekazu, Okuzaki Daisuke, Yamamoto Hirofumi, Doki Yuichiro, Mori Masaki
Department of Surgery, Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.
Department of Surgery, Osaka Rosai Hospital, Osaka, Japan.
Oncol Rep. 2014 Dec;32(6):2354-8. doi: 10.3892/or.2014.3515. Epub 2014 Sep 24.
Serum microRNAs (miRNAs) have been shown to have potential for cancer diagnosis. The main objective of the present study was to identify a novel serum miRNA biomarker from patients with colorectal cancer (CRC). Microarray analysis of miRNA expression was performed using paired pre-operative and post-operative serum from 10 CRC patients. Expression of two miRNAs (let-7a and miR-199a-3p) was significantly decreased in the post-operative serum when compared to levels in the pre-operative serum (P=0.015 and 0.029, respectively). Quantitative real-time polymerase chain reaction (qRT-PCR) confirmed the decrease in the miRNAs in an extended number (n=30) of paired serum samples. Next, we examined the serum let-7a level in 32 non-cancer patients and 84 CRC patients but we found no significant difference (P=0.120). In contrast, miR199a-3p expression was significantly higher in the CRC patients than that in the non-cancer patients (P=0.016). Furthermore, clinical and pathological survey indicated that high expression of miR-199a-3p was significantly associated with deep wall invasion. Our data suggest that circulating miR-199a-3p could be a novel serum biomarker for CRC.
血清微小RNA(miRNA)已被证明具有癌症诊断潜力。本研究的主要目的是从结直肠癌(CRC)患者中鉴定一种新型血清miRNA生物标志物。使用10例CRC患者术前和术后配对血清进行miRNA表达的微阵列分析。与术前血清水平相比,术后血清中两种miRNA(let-7a和miR-199a-3p)的表达显著降低(分别为P=0.015和0.029)。定量实时聚合酶链反应(qRT-PCR)在更多数量(n=30)的配对血清样本中证实了这些miRNA的减少。接下来,我们检测了32例非癌症患者和84例CRC患者的血清let-7a水平,但未发现显著差异(P=0.120)。相反,CRC患者中miR199a-3p的表达明显高于非癌症患者(P=0.016)。此外,临床和病理调查表明,miR-199a-3p的高表达与深层壁浸润显著相关。我们的数据表明,循环miR-199a-3p可能是CRC的一种新型血清生物标志物。