首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >Oncogenic role of long noncoding RNA AF118081 in anti-benzo[a]pyrene-trans-7,8-dihydrodiol-9,10-epoxide-transformed 16HBE cells
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Oncogenic role of long noncoding RNA AF118081 in anti-benzo[a]pyrene-trans-7,8-dihydrodiol-9,10-epoxide-transformed 16HBE cells

机译:长非编码RNA AF118081在抗苯并[a] py-反式-7,8-二氢二醇-9,10-环氧转化的16HBE细胞中的致癌作用

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摘要

Lung cancer is the leading cause of cancer deaths and remains an important public health problem worldwide. Long noncoding RNAs (lncRNAs) are newly identified regulators of tumorigenesis and tumor progression. However, the role of lncRNAs in lung cancer induced by environmental carcinogens remains largely unknown. In this study, an lncRNA microarray was used to compare the expression profiles of malignantly transformed 16HBE cells (16HBE-T) induced with anti-benzo[a]pyrene-trans-7,8-diol-9,10-epoxide (anti-BPDE) and normal 16HBE cells (16HBE-N). Using quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR), lncRNA AF118081 was identified as the most significantly overexpressed lncRNA in 16HBE-T cells, lung cancer cells, and patient samples. Cell proliferation, colony formation, apoptosis, migration, and invasion were assayed in 16HBE-T cells following the knockdown of lncRNA AF118081 with small interfering RNA. AF118081 knockdown inhibited cell growth and tumor invasion. An in vivo (nude mouse) model was then used to assay tumor growth, and the downregulation of AF118081 clearly suppressed tumor growth, consistent with the results of the in vitro assays. Together, these findings identify a new oncogenic lncRNA, lncRNA AF118081, in malignantly transformed 16HBE cells. This enhances our understanding of lncRNAs as important regulatory elements in chemical carcinogenesis and potential targets of lung cancer therapies.
机译:肺癌是导致癌症死亡的主要原因,并且仍然是全球范围内重要的公共卫生问题。长非编码RNA(lncRNA)是新近确定的肿瘤发生和肿瘤进展的调节剂。然而,lncRNAs在环境致癌物诱导的肺癌中的作用仍然未知。在这项研究中,lncRNA芯片用于比较抗苯并[a] py-反式-7,8-二醇-9,10-环氧化物(anti-anti-)诱导的恶性转化的16HBE细胞(16HBE-T)的表达谱BPDE)和正常的16HBE细胞(16HBE-N)。使用定量实时逆转录聚合酶链反应(qRT-PCR),lncRNA AF118081被鉴定为16HBE-T细胞,肺癌细胞和患者样品中最显着过表达的lncRNA。在用小干扰RNA敲低lncRNA AF118081后,在16HBE-T细胞中检测了细胞增殖,集落形成,凋亡,迁移和侵袭。 AF118081组合式抑制细胞生长和肿瘤侵袭。然后使用体内(裸鼠)模型分析肿瘤的生长,AF118081的下调明显抑制了肿瘤的生长,与体外分析的结果一致。总之,这些发现确定了在恶性转化的16HBE细胞中新的致癌lncRNA,即lncRNA AF118081。这增强了我们对lncRNAs作为化学致癌作用和肺癌治疗潜在靶标中重要调控元件的理解。

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