Abstract | BACKGROUND/AIMS: METHODS: The expression profiles of miRNAs in drug-resistant NSCLC cell lines were examined using miRNA sequencing, and the common dysregulated miRNAs in these cell lines were identified and analyzed by bioinformatics methods. RESULTS: A total of 29 upregulated miRNAs and 36 downregulated miRNAs were found in the drug-resistant NSCLC cell lines, of which 26 upregulated and 36 downregulated miRNAs were found to be involved in the Ras signaling pathway. The expression levels, survival analysis, and receiver operating characteristic curve of the dysregulated miRNAs based on The Cancer Genome Atlas database for lung adenocarcinoma showed that hsa-mir-192, hsa-mir-1293, hsa-mir-194, hsa-mir-561, hsa-mir-205, hsa-mir-30a, and hsa-mir-30c were related to lung cancer, whereas only hsa-mir-1293 and hsa-mir-561 were not involved in drug resistance. CONCLUSION: The results of this study may provide novel biomarkers for drug resistance in NSCLC and potential therapies for overcoming drug resistance, and may also reveal the potential mechanisms underlying drug resistance in this disease.
|
Authors | Shousen Hu, Yongliang Yuan, Zhizhen Song, Dan Yan, Xiangzhen Kong |
Journal | Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
(Cell Physiol Biochem)
Vol. 51
Issue 6
Pg. 2509-2522
( 2018)
ISSN: 1421-9778 [Electronic] Germany |
PMID | 30557872
(Publication Type: Journal Article)
|
Copyright | © 2018 The Author(s). Published by S. Karger AG, Basel. |
Chemical References |
- Antineoplastic Agents
- MIRN1293 microRNA, human
- MIRN561 microRNA, human
- MicroRNAs
- Gefitinib
|
Topics |
- Antineoplastic Agents
(pharmacology)
- Carcinoma, Non-Small-Cell Lung
(drug therapy, genetics)
- Cell Line, Tumor
- Drug Resistance, Neoplasm
- Gefitinib
(pharmacology)
- Gene Expression Profiling
- Gene Expression Regulation, Neoplastic
(drug effects)
- Gene Regulatory Networks
(drug effects)
- Humans
- Lung Neoplasms
(drug therapy, genetics)
- MicroRNAs
(genetics)
- Transcriptome
(drug effects)
|