Abstract |
We studied the role of long intergenic non-protein coding RNA 00,511 (LINC00511) in lung adenocarcinoma (LUAD), with a specific focus on acquired chemoresistance. LINC00511 expression was higher in responders to cisplatin (DDP, another name for cisplantin) than non-responders, in A549/DDP cells than in parental A549 cells and normal human bronchial epithelial cells (16HBE). LINC00511 knockdown decreased the half maximal inhibitory concentration (IC50) value, suppressed A549/DDP cell viability, but induced apoptosis. LINC00511 bound with miR-182 and increased the expression of baculoviral inhibitor of apoptosis protein (IAP) repeat containing 5 (BIRC5). BIRC5 knockdown mimicked the effects of LINC00511 knockdown on the IC50 value, A549/DDP cell viability, and apoptosis. BIRC5 overexpression negated the effects of LINC00511 knockdown on A549/DDP cells. In vivo, LINC00511 knockdown attenuated the tumorigenesis of A549/DDP cells after DDP injection. These results provide a novel LINC00511/miR-182/BIRC5 paradigm to explain the mechanism of acquired DDP resistance.
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Authors | Zhongcheng Zhu, Yufeng Shi, Xiaoyi Gong, Jing Li, Mingyun Zhang |
Journal | Molecular biotechnology
(Mol Biotechnol)
Vol. 64
Issue 3
Pg. 252-262
(Mar 2022)
ISSN: 1559-0305 [Electronic] Switzerland |
PMID | 34595724
(Publication Type: Journal Article)
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Copyright | © 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. |
Chemical References |
- BIRC5 protein, human
- MicroRNAs
- Mirn182 microRNA, human
- RNA, Long Noncoding
- RNA, Small Interfering
- Survivin
- Cisplatin
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Topics |
- A549 Cells
- Adenocarcinoma of Lung
(drug therapy, genetics)
- Animals
- Cell Line, Tumor
- Cisplatin
(administration & dosage, pharmacology)
- Down-Regulation
- Drug Resistance, Neoplasm
(drug effects)
- Female
- Gene Expression Regulation, Neoplastic
(drug effects)
- Humans
- Male
- Mice
- MicroRNAs
(genetics)
- RNA, Long Noncoding
(antagonists & inhibitors, genetics)
- RNA, Small Interfering
(administration & dosage, pharmacology)
- Survivin
(genetics)
- Up-Regulation
(drug effects)
- Xenograft Model Antitumor Assays
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