Identification of miRNAs correlating with stage and progression of colorectal cancer

被引：14

作者：

Asadi, Milad ^{[1
,2
]}

Talesh, Shoan Taheri ^{[3
]}

Gjerstorff, Morten Frier ^{[4
]}

Shanehbandi, Dariush ^{[2
]}

Baradaran, Behzad ^{[2
]}

Hashemzadeh, Shahriar ^{[3
,5
]}

Zafari, Venus ^{[6
]}

机构：

[1] Tabriz Univ Med Sci, Liver & Gastrointestinal Dis Res Ctr, Tabriz, Iran

[2] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran

[3] Tabriz Univ Med Sci, Hematol & Oncol Res Ctr, Tabriz, Iran

[4] Univ Southern Denmark, Inst Mol Med, Dept Canc & Inflammat Res, Odense, Denmark

[5] Tabriz Univ Med Sci, Imam Reza Hosp, Dept Gen & Thorac Surg, Tabriz, Iran

[6] Tabriz Univ Med Sci, TB & Lung Dis Res Ctr, Tabriz, Iran

来源：

COLORECTAL CANCER | 2019年 / 8卷 / 02期

关键词：

biomarker; colorectal cancer; diagnosis; miRNA; therapy; PREDICTIVE BIOMARKER; METASTASIS; MICRORNAS; COLON; PROLIFERATION; CARCINOMA; INVASION; GROWTH; GENES; CELLS;

D O I：

10.2217/crc-2018-0014

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Aim: miRNAs control biological processes that are implicated in carcinogenesis, and have been researched as potential biomarkers for colorectal cancer (CRC). The aim of the current study was to evaluate the miRNA expression profile in CRC patients to determine their potential to be used as biomarkers in the disease. Materials & methods: Total 47 tissues and their matched marginal tissues, as control group, were obtained from CRC patients. The transcript levels of a selected panel of 15 cancer-associated miRNAs were quantified via real-time gene expression method. Results: miR-155, miR130a, miR-181b, miR-196a, miR-200c and miR-224 were significantly upregulated, while miR122, miR-132, miR-203b, miR330, miR-323, miR-378a-3p and miR-598 we significantly downregulated in CRC. Conclusion: We identified a panel of miRNAs that may be involved in the etiology and pathogenesis of CRC, and may be used for novel diagnostic and therapeutic strategies.

引用

页数：10

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