Wang Junbin, Gao Jin, Chen Qinnan, Zou Weiyan, Yang Fen, Wei Chenchen, Wang Zhaoxia
Department of Oncology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing 210011, People's Republic of China.
Department of Oncology, The First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, People's Republic of China.
Onco Targets Ther. 2020 Sep 22;13:9333-9348. doi: 10.2147/OTT.S244879. eCollection 2020.
Long non-coding RNAs (lncRNAs) have been found to contribute to cisplatin resistance in several cancers; however, the role of lncRNA LINC01116 in cisplatin resistance remains unknown in non-small-cell lung cancer. This study aimed to examine the contribution of LINC01116 to cisplatin resistance in lung adenocarcinoma (LAD).
Cisplatin-resistant A549/DDP cells were generated by treatment with cisplatin by dose escalation. LINC01116 expression was compared between A549 and A549/DDP cells, and between cisplatin-resistant and non-resistant LAD specimens. The cell viability, colony formation, proliferation, migration and invasion were measured using MTT and Transwell assays, and cell apoptosis and cell cycle were detected using flow cytometry. The expression of E-cadherin and Vimentin was quantified. LAD xenografts were modeled in nude mice to investigate the role of LINC01116 on the resistance of LAD to cisplatin.
MTT assay measured the IC values of 13.49 ± 1.62 and 3.52 ± 1.33 μg/mL for A549/DDP and A549 cells, respectively. LINC01116 was overexpressed in cisplatin-resistant LAD specimens and A549/DDP cells ( < 0.05). Knockdown of LINC01116 inhibited cell viability, proliferation, migration and invasion, promoted apoptosis and enhanced the sensitivity to cisplatin in A549/DDP cells, while LINC01116 overexpression promoted cell viability, proliferation, migration and invasion, inhibited apoptosis and reduced the sensitivity to cisplatin in A549 cells. LINC01116 knockdown resulted in a 2.1-fold increase in E-cadherin expression and a 56% reduction in Vimentin expression in A549/DDP cells, and LINC01116 overexpression resulted in a 45% reduction in E-cadherin expression and a 1.82-fold increase in Vimentin expression in A549 cells.
Dysregulation of lncRNA LINC01116 expression results in resistance of LAD to cisplatin via the EMT process. Our findings support the oncogenic role of LINC01116 to promote the development of cisplatin resistance in LAD, and LINC01116 may be a novel predictor of poor response to cisplatin.
长链非编码RNA(lncRNAs)已被发现与多种癌症的顺铂耐药有关;然而,lncRNA LINC01116在非小细胞肺癌顺铂耐药中的作用尚不清楚。本研究旨在探讨LINC01116在肺腺癌(LAD)顺铂耐药中的作用。
通过剂量递增的顺铂处理产生顺铂耐药的A549/DDP细胞。比较A549和A549/DDP细胞之间以及顺铂耐药和非耐药LAD标本之间LINC01116的表达。使用MTT和Transwell试验测量细胞活力、集落形成、增殖、迁移和侵袭,并使用流式细胞术检测细胞凋亡和细胞周期。定量检测E-钙黏蛋白和波形蛋白的表达。在裸鼠中建立LAD异种移植模型,以研究LINC01116对LAD顺铂耐药性的作用。
MTT试验测得A549/DDP和A549细胞的IC值分别为13.49±1.62和3.52±1.33μg/mL。LINC01116在顺铂耐药的LAD标本和A549/DDP细胞中过表达(<0.05)。敲低LINC01116可抑制A549/DDP细胞的活力、增殖、迁移和侵袭,促进凋亡并增强对顺铂的敏感性,而LINC01116过表达则促进A549细胞的活力、增殖、迁移和侵袭,抑制凋亡并降低对顺铂的敏感性。敲低LINC01116导致A549/DDP细胞中E-钙黏蛋白表达增加2.1倍,波形蛋白表达降低56%,而LINC01116过表达导致A549细胞中E-钙黏蛋白表达降低45%,波形蛋白表达增加1.82倍。
lncRNA LINC01116表达失调通过上皮-间质转化(EMT)过程导致LAD对顺铂耐药。我们的研究结果支持LINC01116在促进LAD顺铂耐药发展中的致癌作用,并且LINC01116可能是顺铂反应不良的一个新的预测指标。