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作 者:刘飞[1] 黄照权[2] 李楠[1] 夏海鸣[1] 黄培林[1]
机构地区:[1]东南大学医学院病理学系,江苏南京210009 [2]右江民族医学院病理学系,广西百色533000
出 处:《现代生物医学进展》2008年第8期1419-1421,1448,共4页Progress in Modern Biomedicine
基 金:右江民族医学院科研基金资助。
摘 要:目的:检测人胃癌细胞系中FHIT基因mRNA的表达状况及构建pcDNA3.1-FHIT真核表达载体。方法:RT-PCR法检测三种不同类型人胃癌细胞系中FHIT基因mRNA的表达,构建真核表达质粒pcDNA3.1-FHIT,通过酶切法、PCR扩增法和DNA序列分析鉴定重组质粒后,用脂质体转染至FHIT基因mRNA阴性表达人胃癌细胞系MKN-45,经G418筛选后RT-PCR鉴定。结果:FHIT基因在人胃癌细胞系BGC-823中呈阳性表达,在MGC-803、MKN-45细胞系中呈阴性表达。FHIT基因cDNA正确克隆到真核细胞表达载体pcDNA3.1中,并成功转染FHIT基因mRNA阴性表达人胃癌细胞系MKN-45。结论:FHIT基因在不同类型人胃癌细胞系中表达各异。成功构建pcDNA3.1-FHIT,并转染到FHIT基因mRNA阴性表达人胃癌细胞系MKN-45,使其FHIT基因阳性表达。Objective:To investigate the expression of FHIT in gastric cancer cell lines and construct recombinant plasmid pcDNA3.1-FHIT and transfect it.Methods:Investigate the expression of FHIT in three gastric cancer cell lines by RT-PCR,clone human FHIT cDNA from a gastric cancer cell line with plasmid pcDNA3.1,to construct eukaryotic expression carrier of recombinant pcDNA3. 1-FHIT,which was transfected into human gastric cancer cell line MKN-45 by liposome after identification by PCR,restriction enzyme digesting and DNA sequencing.The stomach cancer cells were selected by G418,identified by RT-PCR.Results:There was a high expression of FHIT in BGC-823,no expression in MGC-803 and MKN-45.The recombinant plasmid pcDNA3.1 was successfully constructed and transfected intoMKN-45.Conclusions:The different expression levels of FHIT in three stomach cancer cells were conformed and the pcDNA3.1-FHIT has been constructed and transfected successfully,which makes FHIT highly expressed in FHIT-regenerating cell line MKN-45.
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