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RNAi技术对APMCF1基因表达的抑制作用及其对HepG2细胞的影响 被引量:1
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作者 李擒龙 晏伟 +5 位作者 成胜权 王文勇 张志培 王丽 张静 王文亮 《现代肿瘤医学》 CAS 2006年第12期1482-1485,共4页
目的:采用RNAi抑制APMCF1基因表达,并观察其对HepG2细胞生长和细胞周期的影响。方法:根据APMCF1基因序列及其二级结构特征,设计并合成针对APMCF1基因的siRNA寡核苷酸,经退火形成双链后克隆入pSUNeo载体,并采用脂质体介导法将其稳定转染... 目的:采用RNAi抑制APMCF1基因表达,并观察其对HepG2细胞生长和细胞周期的影响。方法:根据APMCF1基因序列及其二级结构特征,设计并合成针对APMCF1基因的siRNA寡核苷酸,经退火形成双链后克隆入pSUNeo载体,并采用脂质体介导法将其稳定转染至人肝癌细胞系HepG2,RT-PCR检测siRNA对靶基因mRNA的抑制效果,然后采用MTT实验、流式细胞仪等对细胞的生长及细胞周期进行观察。结果:HepG2细胞的APMCF1基因表达被成功的抑制。APMCF1基因表达受抑制的HepG2细胞的生长速度加快;细胞周期发生改变,G1期细胞比例减少,S期细胞比例增多,差异具有显著性。结论:HepG2细胞的APMCF1基因表达被成功的抑制。APMCF1基因对HepG2细胞的生长和细胞周期有明显的调节作用,可能是一个侯选的细胞周期调节基因。 展开更多
关键词 apmcf1基因 RNAI 肝细胞肝癌 细胞生长 细胞周期
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外源性APMCF1基因转染对人肝癌细胞系细胞生长和细胞周期的影响 被引量:1
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作者 李擒龙 王文亮 +3 位作者 晏伟 成胜权 王文勇 张志培 《医学研究生学报》 CAS 2005年第12期1069-1072,共4页
目的:探讨外源性APMCF1基因对人肝癌细胞系(HHCC)细胞生长和细胞周期的影响。方法:将人全长APMCF1基因经脂质体包裹转染肝细胞肝癌HHCC细胞,经G418筛选获得转基因癌细胞克隆,采用半定量RT-PCR方法检测APMCF1的表达情况。通过单四唑(MTT... 目的:探讨外源性APMCF1基因对人肝癌细胞系(HHCC)细胞生长和细胞周期的影响。方法:将人全长APMCF1基因经脂质体包裹转染肝细胞肝癌HHCC细胞,经G418筛选获得转基因癌细胞克隆,采用半定量RT-PCR方法检测APMCF1的表达情况。通过单四唑(MTT)比色,绘制生长曲线,观察APMCF1基因对HHCC细胞生长的影响,流式细胞仪检测HHCC细胞周期的变化。结果:半定量RT-PCR结果显示,APMCF1基因被成功地转染至HHCC细胞。稳定表达外源性APMCF1基因的HHCC细胞生长速度明显慢于亲代细胞;细胞周期发生明显改变,G1期细胞比例明显增多,S期细胞比例明显减少。结论:外源性APMCF1基因对HHCC细胞生长和细胞周期有明显的抑制作用,可能是一个细胞周期调节基因。 展开更多
关键词 apmcf1基因 肝细胞肝癌 细胞周期
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Isolation of a novel member of small G protein superfamily and its expression in colon cancer 被引量:5
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作者 Wei Yan Wen-Liang Wang Feng Zhu Sheng-Quan Chen Qing-Long Li Li Wang, Department of Patholology, Xijing Hospital, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China 《World Journal of Gastroenterology》 SCIE CAS CSCD 2003年第8期1719-1724,共6页
AIM: APMCF1 is a novel human gene whose transcripts are up-regulated in apoptotic MCF-7 cells. In order to learn more about this gene′s function in other tumors, we cloned its full length cDNA and prepared its polycl... AIM: APMCF1 is a novel human gene whose transcripts are up-regulated in apoptotic MCF-7 cells. In order to learn more about this gene′s function in other tumors, we cloned its full length cDNA and prepared its polyclonal antibody to investigate its expression in colon cancers with immunohistochemistry.METHODS: With the method of 5′ rapid amplification of cDNA end (RACE) and EST assembled in GenBank, we extended the length of APMCF1 at 5′ end. Then the sequence encoding the APMCF1 protein was amplified by RT-PCR from the total RNA of apoptotic MCF-7 cells and cloned into the prokaryotic expression vector pGEX-KG to construct recombinant expression vector pGEX-APMCF1. The GSTAPMCF1 fusion protein was expressed in E. coli and used to immunize rabbits to get the rabbit anti-APMCF1 serum. The specificity of polyclonal anti-APMCF1 antibody was determined by Western blot. Then we investigated the expression of Apmcf1 in colon cancers and normal colonic mucosa with immunohistochemistry.RESULTS: A cDNA fragment with a length of 1 745 bp was obtained. APMCF1 was mapped to chromosome 3q22.2and spanned at least 14.8 kb of genomic DNA with seven exons and six introns contained. Bioinformatic analysis showed the protein encoded by APMCF1 contained a small GTP-binding protein (G proteins) domain and was homologous to mouse signal recognition particle receptor β(SRβ). A coding region covering 816 bp was cloned and polyclonal anti-APMCF1 antibody was prepared successfully.The immunohistochemistry study showed that APMCF1 had a strong expression in colon cancer.CONCLUSION: APMCF1 may be the gene coding human signal recognition particle receptor β and belongs to the small-G protein superfamily. Its strong expression pattern in colon cancer suggests it may play a role in colon cancer development. 展开更多
关键词 结肠癌 MCF-7细胞 apmcf1基因 G蛋白超家族
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