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首页> 外文期刊>The Journal of laryngology and otology. >Targeted therapy of human laryngeal squamous cell carcinoma in vitro by antisense oligonucleotides directed against telomerase reverse transcriptase mRNA.
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Targeted therapy of human laryngeal squamous cell carcinoma in vitro by antisense oligonucleotides directed against telomerase reverse transcriptase mRNA.

机译:通过针对端粒酶逆转录酶mRNA的反义寡核苷酸体外靶向治疗人喉鳞状细胞癌。

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摘要

A number of different approaches have been developed to inhibit telomerase activity in human cancer cells. In this study, the effect of antisense oligonucleotides (ODNs) by targeting human telomerase reverse transcriptase (hTERT) mRNA in a laryngeal cancer cell line (Hep-2) was investigated. A 20mer antisense oligodeoxynucleotide targeting the most open part of hTERT mRNA (anti-hTERT) and a mismatched control sequence were synthesized. Cells were treated daily with oligonucleotides for up to 72 hours. hTERT mRNA expression was measured by the reverse transcription polymerase chain reaction (RT-PCR) assay; telomerase activity by the telomerase PCR ELISA assay kit (TRAP; Boehringer Mannheim, GmbH, Mannheim, Germany). Cell viability after administration of ODNs was determined using the MTT assay. Morphological changes were examined by haematoxylin and eosin staining. The cell cycle was analyzed using flow cytometry. It was found that antisense treatment induced a decrease in hTERT mRNA expression, telomerase activity, cell growth rate, cell viability, and an increase in apoptosis. The results suggest that inhibition of telomerase activity in Hep-2 cells by short-term antisense treatment against the mRNA of hTERT results in apoptotic cell death. The treatment with anti-hTERT may be useful as a treatment modality for laryngeal squamous carcinoma.
机译:已经开发出许多不同的方法来抑制人类癌细胞中的端粒酶活性。在这项研究中,研究了靶向人端粒酶逆转录酶(hTERT)mRNA在喉癌细胞系(Hep-2)中的反义寡核苷酸(ODN)的作用。合成了靶向hTERT mRNA最开放部分的20mer反义寡聚脱氧核苷酸(anti-hTERT)和错配的控制序列。每天用寡核苷酸处理细胞长达72小时。通过逆转录聚合酶链反应(RT-PCR)法检测hTERT mRNA的表达。通过端粒酶PCR ELISA分析试剂盒(TRAP; Boehringer Mannheim,GmbH,Mannheim,Germany)端粒酶活性。使用MTT测定法确定ODN给药后的细胞生存力。通过苏木精和曙红染色检查形态学变化。使用流式细胞仪分析细胞周期。发现反义处理诱导了hTERT mRNA表达,端粒酶活性,细胞生长速率,细胞活力和凋亡增加的减少。结果表明,通过短期反义处理hTERT mRNA抑制Hep-2细胞端粒酶活性可导致凋亡。抗-hTERT的治疗可用作喉鳞状细胞癌的治疗方法。

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