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首页> 外文期刊>Cellular & molecular biology letters. >The knockdown of c-myc expression by RNAi inhibits cell proliferation in human colon cancer HT-29 cells in vitro and in vivo.
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The knockdown of c-myc expression by RNAi inhibits cell proliferation in human colon cancer HT-29 cells in vitro and in vivo.

机译:RNAi抑制c-myc表达可在体外和体内抑制人结肠癌HT-29细胞中的细胞增殖。

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摘要

We investigated the effects of RNA interference-mediated silencing of the c-myc gene on celluar proliferation and apoptosis in human colon cancer HT-29 cells in vitro and in vivo. A small interfering RNA (siRNA) targeting c-myc was designed, the DNA template was synthesized, and the siRNA was obtained by in vitro transcription. After siRNA transfection into HT-29 and human neuroblastoma IMR-32 cells with Lipofectamine 2000, the proliferation of the HT-29 and IMR-32 cells was assessed via 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) colorimetry, and Hoechst 33258 staining was used to observe cell apoptosis. Following gene transfer to HT-29 cells, the expression of c-myc mRNA was examined via reverse transcription polymerase chain reaction, and the level of the protein via Western blot assay. Growth curves were constructed and in vivo experiments were performed on nude mice to assess the effects of c-myc silencing on tumor growth. The c-myc expression in the tumor tissue was measured by reverse transcription polymerase chain reaction and subsequently by immunohistochemistry. Our paper demonstrates that the delivery of siRNA directed against c-myc not only efficiently down-regulated the expression of c-myc, inhibited the proliferation of HT-29 cells and induced apoptosis in vitro, but also suppressed the growth of colon cancer cells in vivo.
机译:我们研究了RNA干扰介导的c-myc基因沉默对人结肠癌HT-29细胞在体外和体内细胞增殖和凋亡的影响。设计了靶向c-myc的小干扰RNA(siRNA),合成了DNA模板,并通过体外转录获得了siRNA。用Lipofectamine 2000将siRNA转染至HT-29和人神经母细胞瘤IMR-32细胞后,通过3-(4,5-二甲基-2-噻唑基)-2,5评估HT-29和IMR-32细胞的增殖-二苯基-2H-溴化四氮唑(MTT)比色法和Hoechst 33258染色用于观察细胞凋亡。将基因转移至HT-29细胞后,通过逆转录聚合酶链反应检测c-myc mRNA的表达,并通过Western blot检测蛋白的水平。构建生长曲线并在裸鼠上进行体内实验以评估c-myc沉默对肿瘤生长的影响。通过逆转录聚合酶链反应并随后通过免疫组织化学来测量肿瘤组织中的c-myc表达。我们的研究表明,针对c-myc的siRNA的递送不仅能有效下调c-myc的表达,抑制HT-29细胞的增殖并诱导体外凋亡,而且还能抑制结肠癌细胞的生长。体内。

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