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Hsa_circ_0001946通过核苷酸切除修复信号通路抑制非小细胞肺癌的进展并介导顺铂敏感性。

Hsa_circ_0001946 Inhibits Lung Cancer Progression and Mediates Cisplatin Sensitivity in Non-small Cell Lung Cancer via the Nucleotide Excision Repair Signaling Pathway.

作者信息

Huang Ma-Sha, Liu Jun-Yan, Xia Xiao-Bo, Liu Ying-Zi, Li Xi, Yin Ji-Ye, Peng Jing-Bo, Wu Lin, Zhang Wei, Zhou Hong-Hao, Liu Zhao-Qian

机构信息

Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.

Hunan Key Laboratory of Pharmacogenetics, Institute of Clinical Pharmacology, Central South University, Changsha, China.

出版信息

Front Oncol. 2019 Jun 12;9:508. doi: 10.3389/fonc.2019.00508. eCollection 2019.

Abstract

Despite great advances in the diagnosis and treatment of non-small cell lung cancer (NSCLC), early diagnosis remains a challenge because patients usually have advanced lung cancer at the time they are diagnosed. The limited efficacy of conventional chemotherapy is another major problem in the treatment of NSCLC. Based on a published set of sequencing data, we find that hsa_circ_0001946 is a circRNA molecule with a significantly different expression level in three cell lines (human normal lung fibroblasts cell line MRC-5, human NSCLC cell line A549, cisplatin-resistant cell line A549/DDP), NSCLC tissues and paired adjacent normal tissues. We believe that hsa_circ_0001946 may have an effect on the progression of NSCLC and its sensitivity to cisplatin. We focused on investigating the circular RNA, hsa_circ_0001946. RNA interference of hsa_circ_0001946 was carried out in A549 cell lines to determine the effect of reduced hsa_circ_0001946 expression on lung cancer progression and was analyzed by Cell Counting Kit-8 (CCK-8), 5-ethynyl-20-deoxyuridine, clone formation, Hoechst, wound healing, and transwell assays. The nucleotide excision repair (NER) signaling pathway was identified by Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Moreover, cellular responses to cisplatin were assessed through CCK-8 and flow cytometry assays. Western blot analysis and host-cell reactivation assay were used to determine the effect of hsa_circ_0001946 on NER signaling. In this study, we found that the reduced expression of hsa_circ_0001946 promoted the viability, proliferation, migration, and invasion of NSCLC cells, as well as inhibition of cell apoptosis. Our findings suggest that hsa_circ_0001946 can affect the sensitivity of NSCLC cells to the chemotherapeutic drug cisplatin via modulation of the NER signaling pathway. Our study demonstrated the role of hsa_circ_0001946 in NSCLC pathogenesis, development, and chemosensitivity, and suggests that hsa_circ_0001946 may serve as a novel biomarker for the diagnosis and prediction of platinum-based chemosensitivity in patients with NSCLC.

摘要

尽管在非小细胞肺癌(NSCLC)的诊断和治疗方面取得了巨大进展,但早期诊断仍然是一项挑战,因为患者在被诊断时通常已患有晚期肺癌。传统化疗疗效有限是NSCLC治疗中的另一个主要问题。基于一组已发表的测序数据,我们发现hsa_circ_0001946是一种环状RNA分子,在三种细胞系(人正常肺成纤维细胞系MRC-5、人NSCLC细胞系A549、顺铂耐药细胞系A549/DDP)、NSCLC组织及配对的相邻正常组织中表达水平存在显著差异。我们认为hsa_circ_0001946可能对NSCLC的进展及其对顺铂的敏感性有影响。我们专注于研究环状RNA hsa_circ_0001946。在A549细胞系中对hsa_circ_0001946进行RNA干扰,以确定hsa_circ_0001946表达降低对肺癌进展的影响,并通过细胞计数试剂盒-8(CCK-8)、5-乙炔基-2'-脱氧尿苷、克隆形成、Hoechst、伤口愈合和transwell实验进行分析。通过京都基因与基因组百科全书(KEGG)通路分析鉴定核苷酸切除修复(NER)信号通路。此外,通过CCK-8和流式细胞术实验评估细胞对顺铂的反应。采用蛋白质免疫印迹分析和宿主细胞再激活实验来确定hsa_circ_0001946对NER信号的影响。在本研究中,我们发现hsa_circ_0001946表达降低促进了NSCLC细胞的活力、增殖、迁移和侵袭,同时抑制了细胞凋亡。我们的研究结果表明,hsa_circ_0001946可通过调节NER信号通路影响NSCLC细胞对化疗药物顺铂的敏感性。我们的研究证明了hsa_circ_0001946在NSCLC发病机制、发展和化疗敏感性中的作用,并表明hsa_circ_0001946可能作为一种新型生物标志物用于NSCLC患者铂类化疗敏感性的诊断和预测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f3b/6582772/cd98a66f07f2/fonc-09-00508-g0001.jpg

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