| |||||||
ShanghaiTech University Knowledge Management System
MiR-4465 directly targets PTEN to inhibit AKT/mTOR pathway-mediated autophagy | |
2019-01 | |
发表期刊 | CELL STRESS & CHAPERONES (IF:3.3[JCR-2023],3.5[5-Year]) |
ISSN | 1355-8145 |
卷号 | 24期号:1页码:105-113 |
发表状态 | 已发表 |
DOI | 10.1007/s12192-018-0946-6 |
摘要 | Autophagy plays an important role in maintaining cell function. Abnormal autophagy leads to cell dysfunction and is associated with many diseases such as tumors, immunodeficiency diseases, lysosomal storage disorders, and neurodegenerative diseases. Autophagy is precisely regulated, and PTEN plays an important role in regulating autophagy. As noncoding small RNAs, miRNAs play an important role in the fine regulation of cellular processes. However, the mechanism of the miRNA regulation of PTEN-related autophagy has not been fully elucidated. In this study, our results showed that miR-4465 significantly inhibited the expression of PTEN, upregulated phosphorylated AKT, and thereby inhibited autophagy by activating mTOR in HEK293, HeLa, and SH-SY5Y cells. Further studies indicated that miR-4465 reduced PTEN mRNA levels through posttranscriptional regulation via directly targeting the 3-UTR. Our novel findings provide useful hints for the comprehensive elucidation of the molecular mechanism of miRNA-regulated PTEN-related autophagy and may also provide some new insights for the exploration of miRNAs in the treatment of PTEN-related diseases. |
关键词 | Autophagy miR-4465 PTEN mTOR |
收录类别 | SCI ; SCIE |
语种 | 英语 |
资助项目 | Natural Science Foundation of Jiangsu Province[BK20150290] |
WOS研究方向 | Cell Biology |
WOS类目 | Cell Biology |
WOS记录号 | WOS:000457837800010 |
出版者 | SPRINGER |
WOS关键词 | CELL LUNG-CANCER ; GENE ; METASTASIS ; RAPAMYCIN ; BREAST |
原始文献类型 | Article |
引用统计 | 正在获取...
|
文献类型 | 期刊论文 |
条目标识符 | https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/30243 |
专题 | 生命科学与技术学院_博士生 生命科学与技术学院_硕士生 |
通讯作者 | Wang, Mei |
作者单位 | 1.Soochow Univ, Childrens Hosp, Dept Pharm, 92 Zhongnan St, Suzhou, Peoples R China 2.Chinese Acad Sci, Shanghai Inst Materia Med, State Key Lab Drug Res, Ctr Drug Safety Evaluat & Res, Shanghai, Peoples R China 3.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai, Peoples R China 4.Soochow Univ, Jiangsu Key Lab Neuropsychiat Dis, Lab Mol Neuropathol, Suzhou 215021, Peoples R China 5.Soochow Univ, Coll Pharmaceut Sci, Suzhou 215021, Peoples R China |
推荐引用方式 GB/T 7714 | Tao, Zhouteng,Feng, Chenxi,Mao, Chenmei,et al. MiR-4465 directly targets PTEN to inhibit AKT/mTOR pathway-mediated autophagy[J]. CELL STRESS & CHAPERONES,2019,24(1):105-113. |
APA | Tao, Zhouteng.,Feng, Chenxi.,Mao, Chenmei.,Ren, Jin.,Tai, Yusi.,...&Wang, Mei.(2019).MiR-4465 directly targets PTEN to inhibit AKT/mTOR pathway-mediated autophagy.CELL STRESS & CHAPERONES,24(1),105-113. |
MLA | Tao, Zhouteng,et al."MiR-4465 directly targets PTEN to inhibit AKT/mTOR pathway-mediated autophagy".CELL STRESS & CHAPERONES 24.1(2019):105-113. |
条目包含的文件 | ||||||
文件名称/大小 | 文献类型 | 版本类型 | 开放类型 | 使用许可 |
修改评论
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。