miR-194 Inhibits the Proliferation of SW620 Colon Cancer Stem Cells Through Downregulation of SSH2 Expression

• Published in: Cancer management and research Vol. 11; pp. 10229 - 10238
• Main Authors: Sun, Bo, Fang, Yan-Tian, Jin, Dan-Juan, Chen, Zong-You, Li, Zhen-Yang, Gu, Xiao-Dong, Xiang, Jian-Bin
• Format: Journal Article
• Language: English
• Published: New Zealand Dove Medical Press Limited 01.12.2019; Dove; Dove Medical Press
• Subjects: Cell cycle; Colon cancer; Colorectal cancer; Health aspects; Journalists; Luciferase; mir-194; Novels; Original Research; proliferation; RNA; ssh2; stem cell; Stem cell transplantation; Stem cells; Tumors; China; miR-194; colorectal cancer; proliferation; stem cell; SSH2
• ISSN: 1179-1322; 1179-1322
• DOI: 10.2147/CMAR.S221150

Colorectal cancer (CRC) stem cells are tumorigenic, capable of self-renewal, and resistant to therapy. Although the expression pattern and functions of micro RNA (miR)-194 in CRC cells have been widely investigated, little is known about its role in CRC stem cells. Therefore, the aim of this study was to investigate the potential role of miR-194 in CRC stem cells. CRC stem cells were isolated from the SW620 colon cancer cell line using microbeads. The expression levels of miR-194 and slingshot 2 (SSH2) in CRC stem cells were detected by RT-PCR and Western blot. A luciferase reporter assay was performed to confirm that miR-194 directly targets . Proliferation of CRC stem cells was examined by colony formation and MTT assays. Apoptosis in CRC stem cells was detected by cell cycle and apoptosis assays. The role of miR-194 in tumor growth was determined in vivo. Cells positive for CD44 and CD133 accounted for approximately 88.7% of the isolated population after microbead isolation. We reveal for the first time that miR-194 expression is decreased in CRC stem cells. Specifically, miR-194 is involved in inhibiting the proliferation of CRC stem cells and promoting CRC stem cell apoptosis by directly targeting . Furthermore, overexpression of miR-194 resulted in blocking the G1/S transition, the induction of cellular apoptotic process, thereby suppressing the malignant behaviors of CRC stem cells. This study represents a novel characterization of miR-194 function in CRC stem cells, which may aid in the development of promising therapeutic strategies targeting CRC.