دورية أكاديمية

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

التفاصيل البيبلوغرافية
العنوان: Tumor Suppressive Effects of miR-124 and Its Function in Neuronal Development
المؤلفون: Rikako Sanuki, Tomonori Yamamura
المصدر: International Journal of Molecular Sciences, Vol 22, Iss 11, p 5919 (2021)
بيانات النشر: MDPI AG, 2021.
سنة النشر: 2021
المجموعة: LCC:Biology (General)
LCC:Chemistry
مصطلحات موضوعية: microRNA-124, tumor suppression, EMT, metastasis, neuronal development, Biology (General), QH301-705.5, Chemistry, QD1-999
الوصف: 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.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 22115919
1422-0067
1661-6596
العلاقة: https://www.mdpi.com/1422-0067/22/11/5919Test; https://doaj.org/toc/1661-6596Test; https://doaj.org/toc/1422-0067Test
DOI: 10.3390/ijms22115919
الوصول الحر: https://doaj.org/article/37795f9faaaf463782501fe2ddaabc96Test
رقم الانضمام: edsdoj.37795f9faaaf463782501fe2ddaabc96
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22115919
14220067
16616596
DOI:10.3390/ijms22115919