Ghanbari Reza, Mosakhani Neda, Asadi Jahanbakhsh, Nouraee Nazila, Mowla Seyed Javad, Yazdani Yaghoub, Mohamadkhani Ashraf, Poustchi Hossein, Knuutila Sakari, Malekzadeh Reza
Faculty of Advanced Medical Technologies, Golestan University of Medical Sciences, Gorgan, IR Iran ; Digestive Oncology Research Center, Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, IR Iran.
Department of Pathology, Haartman Institute, Helsinki University, Helsinki, Finland.
Iran J Cancer Prev. 2015 May;8(3):e2329. doi: 10.17795/ijcp2329. Epub 2015 May 22.
Colorectal cancer is one of the most commonly diagnosed cancers and cancer- related death worldwide. Identification of new specific biomarkers could be helpful to detection of this malignancy. Altered plasma microRNA expression has been identified in many cancers, including colorectal cancer.
The main objective of this study was to identify the circulating microRNAs with the most expression changes in colorectal cancer patients compared with neoplasm free healthy individuals.
MicroRNA expression profiling was performed on plasma samples of 37 colorectal cancer patients and 8 normal subjects using microRNA microarray. Quantitative real-time reverse transcription polymerase chain reaction was used to validate the two selected altered microR NAs. Plasma samples from 61 colorectal cancer patients and 24 normal subjects were used in our validation study.
In profiling study we found a panel of six plasma microRNAs with significant downregulation. MicroRNA-142-3p and microRNA-26a-5p were selected and validated by polymerase chain reaction. Our results demonstrated that expression levels of plasma microRNA-142-3p and microRNA-26a-5p were significantly downregulated in patients with colorectal cancer when compared to control group.
Our findings suggest that downregulation of plasma microRNA-142-3p and microRNA-26a-5p might serve as novel noninvasive biomarkers in the diagnosis of colorectal cancer, although more studies are needed to highlight the theoretical strengths.
结直肠癌是全球最常被诊断出的癌症之一,也是与癌症相关死亡的主要原因之一。鉴定新的特异性生物标志物有助于检测这种恶性肿瘤。在包括结直肠癌在内的许多癌症中,血浆微小RNA表达均发生了改变。
本研究的主要目的是鉴定与无肿瘤的健康个体相比,结直肠癌患者中表达变化最大的循环微小RNA。
使用微小RNA微阵列对37例结直肠癌患者和8例正常受试者的血浆样本进行微小RNA表达谱分析。采用定量实时逆转录聚合酶链反应来验证两个选定的改变的微小RNA。我们的验证研究使用了61例结直肠癌患者和24例正常受试者的血浆样本。
在分析研究中,我们发现一组6种血浆微小RNA显著下调。选择微小RNA-142-3p和微小RNA-26a-5p并通过聚合酶链反应进行验证。我们的结果表明,与对照组相比,结直肠癌患者血浆微小RNA-142-3p和微小RNA-26a-5p的表达水平显著下调。
我们的研究结果表明,血浆微小RNA-142-3p和微小RNA-26a-5p的下调可能作为结直肠癌诊断中的新型非侵入性生物标志物,尽管需要更多研究来突出其理论优势。