Inhibition of the AKT/mTOR pathway negatively regulates PTEN expression via miRNAs

Bibliographic Details
Title: Inhibition of the AKT/mTOR pathway negatively regulates PTEN expression via miRNAs
Authors: Wan Linyan, Wang Yanan, Li Jie, Wang Yani, Zhang Hongbing
Source: Acta Biochimica et Biophysica Sinica, Vol 54, Pp 1637-1647 (2022)
Publisher Information: China Science Publishing & Media Ltd., 2022.
Publication Year: 2022
Collection: LCC:Biochemistry
LCC:Genetics
Subject Terms: miRNA, PI3K/AKT/mTOR, PTEN, Biochemistry, QD415-436, Genetics, QH426-470
More Details: PI3K/AKT/mTOR pathway plays important roles in cancer development, and the negative role of PTEN in the PI3K/AKT/mTOR pathway is well known, but whether PTEN can be inversely regulated by PI3K/AKT/mTOR has rarely been reported. Here we aim to investigate the potential regulatory relationship between PTEN and Akt/mTOR inhibition in MEFs. AKT1 E17K and TSC2 –/– MEFs were treated with the AKT inhibitor MK2206 and the mTOR inhibitors rapamycin and Torin2. Our results reveal that inhibition of AKT or mTOR suppresses PTEN expression in AKT1 E17K and TSC2 –/– MEFs, but the transcription, subcellular localization, eIF4E-dependent translational initiation or lysosome- and proteasome-mediated degradation of PTEN change little, as shown by the real time PCR, nucleus cytoplasm separation assay and immunofluorescence analysis. Moreover, mTOR suppression leads to augmentation of mouse PTEN-3′UTR-binding miRNAs, including miR-23a-3p, miR-23b-3p, miR-25-3p and miR-26a-5p, as shown by the dual luciferase reporter assay and miRNA array analysis, and miRNA inhibitors collaborately rescue the decline of PTEN level. Collectively, our findings confirm that inhibition of mTOR suppresses PTEN expression by upregulating miRNAs, provide a novel explanation for the limited efficacy of mTOR inhibitors in the treatment of mTOR activation-related tumors, and indicate that dual inhibition of mTOR and miRNA is a promising therapeutic strategy to overcome the resistance of mTOR-related cancer treatment.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1672-9145
53248309
Relation: https://doaj.org/toc/1672-9145
DOI: 10.3724/abbs.2022159
Access URL: https://doaj.org/article/2a99ed65d532483090cc348c83be7f62
Accession Number: edsdoj.2a99ed65d532483090cc348c83be7f62
Database: Directory of Open Access Journals
More Details
ISSN:16729145
53248309
DOI:10.3724/abbs.2022159
Published in:Acta Biochimica et Biophysica Sinica
Language:English