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作 者:张桓瑜[1] 梁铸林[1] 郑丽端[2] 童强松[1] 董继华[3]
机构地区:[1]华中科技大学同济医学院附属协和医院外科,武汉430022 [2]华中科技大学同济医学院附属协和医院病理科,武汉430022 [3]华中科技大学同济医学院附属协和医院中心实验室,武汉430022
出 处:《中华实验外科杂志》2011年第4期571-573,共3页Chinese Journal of Experimental Surgery
基 金:基金项目:国家自然科学基金资助项目(30200284、30600278、30772359、81071997、81072073);教育部“新世纪优秀人才支持计划”资助项目(NCET-06-0641);教育部回国人员基金资助项目(2008889)
摘 要:目的构建人微小RNAl45(miR-145)前体的真核表达载体,探讨其对胃癌细胞生物学行为的影响。方法根据人pre-miR-145序列,合成两条互补的寡核苷酸链,退火后连接人pPG-miR-EGFP载体,转化扩增后进行测序鉴定;重组质粒在阳离子脂质体Lipofectamine2000的介导下,瞬时转染人胃癌细胞株SGC-7901,实时定量聚合酶链反应(PCR)检测细胞中miR.145表达水平,黏附实验和Transwell小室实验检测癌细胞游走、侵袭能力。结果所构建的pPG—miRl45-EGFP载体中插入基因片段与设计序列完全匹配;重组质粒转染SGC.7901细胞后,miR-145表达分别上调20.45倍(P〈0.01),细胞黏附能力分别下降51.5%(P〈0.01),细胞侵袭能力分别下降30.4%(P〈0.01)。结论成功构建人pre—miR-145真核表达载体,转染胃癌细胞过表达后,能抑制癌细胞的游走和侵袭能力。Objective To construct the eukaryotic expression vector of miR-145 and explore its effects on the biological behavior of gastric cancer. Methods According to the pre-miR-145 sequence, two complementary oligonucleotide strands were synthesized and inserted into pPG-miR-EGFP vector, which was validated by nucleic acid sequencing. Under the induction of Lipofectamine 2000, the recombinant was transfected into SGC-7901 cells. The expression level of miR-145 was detected by real-time reverse tran- scription-polymerase chain reaction (RT-PCR). The cell adhesion and transwell assays were applied for the detection of in vitro migration and invasion of cancer cells. Results Sequencing analysis confirmed the cor- rectness of the construction. Compared with negative control,the expression of miR-145 was upregulated by 20.45 times ( P 〈 0. 01 ). Meanwhile, the cellular adhesion was downregulated by 51.5 % ( P 〈 0. 01 ), and the invasive activity was downregulated by 30. 4% (P 〈 0. 01 ). Conclusion The expression vector of pre- miR-145 was successfully constructed,and induced the miR-145 overexpression in gastric cancer cells,resuiting in decrease of migration and invasion of cancer cells.
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