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MiR-122-5p regulates the mevalonate pathway by targeting p53 in non-small cell lung cancer.
- Source :
-
Cell death & disease [Cell Death Dis] 2023 Apr 01; Vol. 14 (4), pp. 234. Date of Electronic Publication: 2023 Apr 01. - Publication Year :
- 2023
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Abstract
- The 5-year survival rate of non-small cell lung cancer (NSCLC) patients is very low. MicroRNAs (miRNAs) are involved in the occurrence of NSCLC. miR-122-5p interacts with wild-type p53 (wtp53), and wtp53 affects tumor growth by inhibiting the mevalonate (MVA) pathway. Therefore, this study aimed to evaluate the role of these factors in NSCLC. The role of miR-122-5p and p53 was established in samples from NSCLC patients, and human NSCLC cells A549 using the miR-122-5p inhibitor, miR-122-5p mimic, and si-p53. Our results showed that inhibiting miR-122-5p expression led to the activation of p53. This inhibited the progression of the MVA pathway in the NSCLC cells A549, hindered cell proliferation and migration, and promoted apoptosis. miR-122-5p was negatively correlated with p53 expression in p53 wild-type NSCLC patients. The expression of key genes in the MVA pathway in tumors of p53 wild-type NSCLC patients was not always higher than the corresponding normal tissues. The malignancy of NSCLC was positively correlated with the high expression of the key genes in the MVA pathway. Therefore, miR-122-5p regulated NSCLC by targeting p53, providing potential molecular targets for developing targeted drugs.<br /> (© 2023. The Author(s).)
- Subjects :
- Humans
Mevalonic Acid
Tumor Suppressor Protein p53 genetics
Tumor Suppressor Protein p53 metabolism
Cell Proliferation genetics
Gene Expression Regulation, Neoplastic
Cell Movement genetics
Cell Line, Tumor
Carcinoma, Non-Small-Cell Lung pathology
Lung Neoplasms pathology
MicroRNAs genetics
MicroRNAs metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-4889
- Volume :
- 14
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cell death & disease
- Publication Type :
- Academic Journal
- Accession number :
- 37005437
- Full Text :
- https://doi.org/10.1038/s41419-023-05761-9