Volume 26, Issue 1 921907 pp. 27-34
Article
Open Access

Clinicopathological Significance of microRNA-31, -143 and -145 Expression in Colorectal Cancer

Chao-Jie Wang

Chao-Jie Wang

Institute of Digestive Surgery and Department of Colorectal Surgery and State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu, China

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Zong-Guang Zhou

Zong-Guang Zhou

Institute of Digestive Surgery and Department of Colorectal Surgery and State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu, China

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Ling Wang

Ling Wang

Institute of Digestive Surgery and Department of Colorectal Surgery and State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu, China

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Lie Yang

Lie Yang

Institute of Digestive Surgery and Department of Colorectal Surgery and State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu, China

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Bin Zhou

Bin Zhou

Institute of Digestive Surgery and Department of Colorectal Surgery and State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu, China

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Jun Gu

Jun Gu

Institute of Digestive Surgery and Department of Colorectal Surgery and State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu, China

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Hong-Ying Chen

Hong-Ying Chen

Institute of Digestive Surgery and Department of Colorectal Surgery and State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu, China

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Xiao-Feng Sun

Corresponding Author

Xiao-Feng Sun

Institute of Digestive Surgery and Department of Colorectal Surgery and State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu, China

Department of Oncology Institute of Clinical and Experimental Medicine University of Linköping Linköping, Sweden

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First published: 03 June 2013
Citations: 5

Abstract

We are just beginning to understand how microRNAs (miRNAs) are involved in tumor-related processes in humans. Applying real-time RT-PCR, we investigated the miR-31, miR-143 and miR-145 expression in 98 primary CRC specimens, along with the corresponding normal mucosa specimens, and analyze the relationship of their expression with clinicopathological features. Our results showed the miR-31 expression was up-regulated in CRC compared to normal mucosa (p = 0.001). Furthermore, miR-31 expression was positively related to advanced TNM stage (p = 0.026) and deeper invasion of tumors (p = 0.024). MiR-145 was down-regulated in both colon (p = 0.001) and rectal (p = 0.012) cancer. MiR-143 was only down-regulated in colon cancer (p = 0.023) but not in rectal cancer (p = 0.351). There was no relationship of miR-143 and miR-145 expression with other clinicopathological features (p > 0.05), except that the miR-145 expression was related to cancer site (p = 0.03). In conclusion, the miR-31 overexpression may be involved in the development and progression of CRC. The miR-143 and miR-145 may play a certain role in the development of colon and/or rectal cancers but not in progression of the disease.

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