首页> 外文期刊>World Journal of Gastroenterology >Combination of telomerase antisense oligonucleotides simultaneously targeting hTR and hTERT produces synergism of inhibition of telomerase activity and growth in human colon cancer cell line.
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Combination of telomerase antisense oligonucleotides simultaneously targeting hTR and hTERT produces synergism of inhibition of telomerase activity and growth in human colon cancer cell line.

机译:同时靶向hTR和hTERT的端粒酶反义寡核苷酸的组合产生抑制人结肠癌细胞系中端粒酶活性和生长的协同作用。

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AIM: To investigate synergism of inhibition of telomerase activity and proliferation of human colon cancer cells by combination of telomerase antisense oligonucleotides (ASODNs) simultaneously targeting human telomerase RNA (hTR) and human telomerase reverse transcriptase (hTERT) in vitro. METHODS: ASODN of hTR and ASODN of hTERT were transfected into human colon cancer SW480 cells by liposomal transfection reagents. Telomerase activity of SW480 cells was examined using telomeric repeat amplification protocol (TRAP)-enzyme-linked immunosorbent assay (PCR-ELISA). Proliferation activity of SW480 cells was tested by methyl thiazolyl tetrazolium assay. Apoptosis and cell cycle were analyzed by flow cytometry. RESULTS: The telomerase activity and cell survival rate in SW480 cells transfected with 0.2 mumol/L of ASODN of hTR or ASODN of hTERT for 24-72 h were significantly decreased in a time-dependent manner compared with those after treatment with sense oligonucleotides and untreated (telomerase activity: 24 h, 73%, 74% vs 99%, 98%; 48 h, 61%, 55% vs 98%, 99%; 72 h, 41%, 37% vs 99%, 97%; P<0.01; cell survival rate: 24 h, 88%, 86% vs 94%, 98%; 48 h, 49%, 47% vs 94%, 97%; 72 h, 44%, 42% vs 92%, 96%; P<0.01). Moreover, the telomerase activity and the cell survival rate in SW480 cells treated by the combination of telomerase anti-hTR and anti-hTERT were more significantly suppressed than single anti-hTR or anti-hTERT (telomerase activity: 24 h, 59% vs 73%, 74%; 48 h, 43% vs 61%, 55%; 72 h, 18% vs 41%, 37%; P<0.01; cell survival rate: 24 h, 64% vs 88%, 86%; 48 h, 37% vs 49%, 47%; 72 h, 25% vs 44%, 42%; P<0.01). Meanwhile, the apoptosis rates in the combination group were markedly increased compared with those in the single group (24 h, 18.0% vs 7.2%, 7.4%; 48 h, 23.0% vs 13.0%, 14.0%; 72 h, 28.6% vs 13.2%, 13.75; P<0.01). Cells in combination group were arrested at G(0)/G(1) phase. CONCLUSION: Telomerase anti-hRT and anti-hTERT suppress telomerase activity, and inhibit growth of human colon cancer cells probably via induction of apoptosis and retardation of cell cycle. Additionally, combined use of telomerase ASODNs targeting both hTR and hTERT yields synergistic action selective for human colon cancer.
机译:目的:通过体外同时靶向人端粒酶RNA(hTR)和人端粒酶逆转录酶(hTERT)的端粒酶反义寡核苷酸(ASODN)的组合,研究抑制端粒酶活性和人类结肠癌细胞增殖的协同作用。方法:脂质体转染试剂将hTR的ASODN和hTERT的ASODN转染人结肠癌SW480细胞。使用端粒重复扩增方案(TRAP)-酶联免疫吸附测定(PCR-ELISA)检测SW480细胞的端粒酶活性。通过甲基噻唑基四唑鎓测定法测试SW480细胞的增殖活性。通过流式细胞术分析细胞凋亡和细胞周期。结果:转染了0.2μmol/ L hTR的ASODN或hTERT的ASODN的SW480细胞中,端粒酶活性和细胞存活率与有义寡核苷酸处理和未经处理的相比,以时间依赖性显着降低,时间为24-72 h。 (端粒酶活性:24 h,73%,74%vs 99%,98%; 48 h,61%,55%vs 98%,99%; 72 h,41%,37%vs 99%,97%; P <0.01;细胞存活率:24小时,88%,86%与94%,98%; 48小时,49%,47%与94%,97%; 72小时,44%,42%与92%,96 %; P <0.01)。此外,端粒酶抗-hTR和抗-hTERT联合处理后,SW480细胞的端粒酶活性和细胞存活率比单一抗-hTR或抗-hTERT受到更显着的抑制(端粒酶活性:24 h,59%vs 73) %,74%; 48 h,43%vs 61%,55%; 72 h,18%vs 41%,37%; P <0.01;细胞存活率:24 h,64%vs 88%,86%; 48 h,37%vs 49%,47%; 72 h,25%vs 44%,42%; P <0.01)。同时,联合组的细胞凋亡率明显高于单一组(24 h,18.0%vs 7.2%,7.4%; 48 h,23.0%vs 13.0%,14.0%; 72 h,28.6%vs。 13.2%,13.75; P <0.01)。组合组中的细胞停在G(0)/ G(1)阶段。结论:端粒酶抗hRT和抗hTERT抑制端粒酶活性,并可能通过诱导细胞凋亡和延迟细胞周期来抑制人结肠癌细胞的生长。此外,靶向hTR和hTERT的端粒酶ASODN的联合使用可产生对人类结肠癌有选择性的协同作用。

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