Tumor Suppressive Effects of miR-124 and Its Function in Neuronal Development

被引:31
作者
Sanuki, Rikako [1 ]
Yamamura, Tomonori [1 ]
机构
[1] Kyoto Inst Technol, Dept Appl Biol, Ukyo Ku, Saga Ippongi Cho 1, Kyoto 6168354, Japan
基金
日本学术振兴会;
关键词
microRNA-124; tumor suppression; EMT; metastasis; neuronal development; EPITHELIAL-MESENCHYMAL TRANSITION; INHIBITS CELL-PROLIFERATION; LUNG-CANCER CELLS; HUMAN HEPATOCELLULAR-CARCINOMA; DOWN-REGULATION; COLORECTAL-CANCER; BREAST-CANCER; GASTRIC-CANCER; EXPRESSION PROFILES; UP-REGULATION;
D O I
10.3390/ijms22115919
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNA-124 (miR-124) is strongly expressed in neurons, and its expression increases as neurons mature. Through DNA methylation in the miR-124 promoter region and adsorption of miR-124 by non-coding RNAs, miR-124 expression is known to be reduced in many cancer cells, especially with high malignancy. Recently, numerous studies have focused on miR-124 due to its promising tumor-suppressive effects; however, the overview of their results is unclear. We surveyed the tumor-suppressive effect of miR-124 in glial cell lineage cancers, which are the most frequently reported cancer types involving miR-124, and in lung, colon, liver, stomach, and breast cancers, which are the top five causes of cancer death. Reportedly, miR-124 not only inhibits proliferation and accelerates apoptosis, but also comprehensively suppresses tumor malignant transformation. Moreover, we found that miR-124 exerts its anti-tumor effects by regulating a wide range of target genes, most notably STAT3 and EZH2. In addition, when compared to the original role of miR-124 in neuronal development, we found that the miR-124 target genes that contribute to neuronal maturation share similarities with genes that cause cancer cell metastasis and epithelial-mesenchymal transition. We believe that the two apparently unrelated fields, cancer and neuronal development, can bring new discoveries to each other through the study of miR-124.
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页数:15
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