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MicroRNA‐203 diminishes the stemness of human colon cancer cells by suppressing GATA6 expression
- Source :
- Journal of Cellular Physiology. 235:2866-2880
- Publication Year :
- 2019
- Publisher :
- Wiley, 2019.
-
Abstract
- The interaction between hyaluronan and CD44, an important cancer stem-cell marker, stimulates various tumor cell-specific functions such as the stemness of tumor cells. microRNA-203 (miR-203) can be downregulated by this interaction in human colorectal cancer (CRC) cells, which increases their stemness; however, the underlying mechanism is not yet defined. Here, we show that overexpression and sequestration of miR-203 in HCT-116 and HT-29 human CRC cells reduces and enhances their stemness, respectively. We also show that GATA-binding factor 6 (GATA6) is a direct target of miR-203. Our results indicate that upregulated expression of this transcription factor not only restores the self-renewal abilities of miR-203-overexpressing HCT-116 and HT-29 cells but also promotes the stemness properties of their parental counterparts. More important, we show that silencing the expression of either LRH-1 or Hes-1 is sufficient to diminish the stemness-promoting effects of GATA6 in human CRC cells. Together, our findings delineate the stemness-inhibitory mechanism of miR-203 in human CRC cells and suggest that this miR is a potential therapeutic agent for colorectal cancer.
- Subjects :
- 0301 basic medicine
Physiology
Colorectal cancer
Clinical Biochemistry
Down-Regulation
Biology
03 medical and health sciences
0302 clinical medicine
Cell Line, Tumor
GATA6 Transcription Factor
microRNA
medicine
Humans
Gene silencing
Transcription factor
GATA6
CD44
Cancer
Cell Biology
medicine.disease
Up-Regulation
Gene Expression Regulation, Neoplastic
MicroRNAs
030104 developmental biology
030220 oncology & carcinogenesis
Neoplastic Stem Cells
Cancer research
biology.protein
Colorectal Neoplasms
miR-203
Subjects
Details
- ISSN :
- 10974652 and 00219541
- Volume :
- 235
- Database :
- OpenAIRE
- Journal :
- Journal of Cellular Physiology
- Accession number :
- edsair.doi.dedup.....5ff4f1df44ad5f807a542fffe0bd2ded