Abstract |
Mutations in the epidermal growth factor receptor (EGFR) make lung adenocarcinoma cells sensitive to EGFR tyrosine kinase inhibitors (TKIs). Long-term cancer therapy may cause the occurrence of acquired resistance to EGFR TKIs. Long non-coding RNAs (lncRNAs) play important roles in tumor formation, tumor metastasis and the development of EGFR-TKI resistance in lung cancer. To gain insight into the molecular mechanisms of EGFR-TKI resistance, we generated an EGFR-TKI-resistant HCC827-8-1 cell line and analyzed expression patterns by lncRNA microarray and compared it with its parental HCC827 cell line. A total of 1,476 lncRNA transcripts and 1,026 mRNA transcripts were dysregulated in the HCC827‑8-1 cells. The expression levels of 7 chosen lncRNAs were validated by real-time quantitative PCR. As indicated by functional analysis, several groups of lncRNAs may be involved in the bio-pathways associated with EGFR-TKI resistance through their cis- and/or trans‑regulation of protein-coding genes. Thus, lncRNAs may be used as novel candidate biomarkers and potential targets in EGFR-TKI therapy in the future.
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Authors | Ying Wu, Dan-Dan Yu, Yong Hu, Dali Yan, Xiu Chen, Hai-Xia Cao, Shao-Rong Yu, Zhuo Wang, Ji-Feng Feng |
Journal | Oncology reports
(Oncol Rep)
Vol. 35
Issue 6
Pg. 3371-86
(Jun 2016)
ISSN: 1791-2431 [Electronic] Greece |
PMID | 27108960
(Publication Type: Journal Article)
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Chemical References |
- E2F1 Transcription Factor
- E2F1 protein, human
- MicroRNAs
- Protein Kinase Inhibitors
- RNA, Long Noncoding
- USF1 protein, human
- Upstream Stimulatory Factors
- EGFR protein, human
- ErbB Receptors
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Topics |
- Adenocarcinoma
(drug therapy, genetics)
- Adenocarcinoma of Lung
- Cell Line, Tumor
- Drug Resistance, Neoplasm
- E2F1 Transcription Factor
(physiology)
- ErbB Receptors
(antagonists & inhibitors)
- Humans
- Lung Neoplasms
(drug therapy, genetics)
- MicroRNAs
(analysis)
- Oligonucleotide Array Sequence Analysis
- Protein Kinase Inhibitors
(therapeutic use)
- RNA, Long Noncoding
(analysis)
- Real-Time Polymerase Chain Reaction
- Upstream Stimulatory Factors
(physiology)
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