Abstract
Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are used clinically as target therapies for lung cancer patients, but the occurrence of acquired drug resistance limits their efficacy. Nicotinamide N-methyltransferase (NNMT), a cancer-associated metabolic enzyme, is commonly overexpressed in various human tumors. Emerging evidence also suggests a crucial loss of function of microRNAs (miRNAs) in modulating tumor progression in response to standard therapies. However, their precise roles in regulating the development of drug-resistant tumorigenesis are still poorly understood. Herein, we established EGFR-TKI-resistant non-small-cell lung cancer (NSCLC) models and observed a negative correlation between the expression levels of NNMT and miR-449a in tumor cells. Additionally, knockdown of NNMT suppressed p-Akt and tumorigenesis, while re-expression of miR-449a induced phosphatase and tensin homolog (PTEN), and inhibited tumor growth. Furthermore, yuanhuadine, an antitumor agent, significantly upregulated miR-449a levels while critically suppressing NNMT expression. These findings suggest a novel therapeutic approach for overcoming EGFR-TKI resistance to NSCLC treatment.
Original language | English |
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Pages (from-to) | 455-467 |
Number of pages | 13 |
Journal | Molecular Therapy - Nucleic Acids |
Volume | 11 |
DOIs | |
Publication status | Published - 1 Jun 2018 |
Bibliographical note
Publisher Copyright:© 2018 The Authors
Keywords
- docking
- EGFR-TKI
- gefitinib resistance
- methylation
- miR-449a
- NNMT
- non-small-cell lung cancer
- NSCLC
- PTEN/PI3K/Akt
- yuanhuadine