基础医学与临床
基礎醫學與臨床
기출의학여림상
BASIC MEDICAL SCIENCES AND CLINICS
2009年
12期
1286-1290
,共5页
冯俊飞%董坚%洪敏%高嫦娥
馮俊飛%董堅%洪敏%高嫦娥
풍준비%동견%홍민%고항아
乳腺癌%CXCR4%小干扰RNA%RNA干扰
乳腺癌%CXCR4%小榦擾RNA%RNA榦擾
유선암%CXCR4%소간우RNA%RNA간우
breast cancer%CXCR4%siRNA%RNAi
目的 构建趋化因子受体(CXCR4)小分子干扰RNA(siRNA)表达载体,研究其对体外乳腺癌细胞侵袭能力的影响.方法 选择CXCR4高表达的乳腺癌MDA-MB-231细胞系,设计合成人CXCR4基因不同靶点的能编码siRNA的2条双链DNA序列,克隆到真核表达载体pGE-1-U6/kna中构建siRNA表达载体,体外脂质体介导转染MDA-MB-231细胞,用Western blot分析CXCR4蛋白表达,Transwell小室检测细胞的侵袭能力.结果 成功构建了CXCR4-siRNA表达载体,瞬时转染乳腺癌细胞后能显著降低CXCR4的蛋白表达,可有效抑制人类乳腺癌MDA-MB-231细胞的侵袭能力.结论 CXCR4-siRNA表达载体通过降低CXCR4基因的蛋白表达能显著抑制人类乳腺癌细胞的侵袭能力,有望为乳腺癌转移的基因治疗开辟新途径.
目的 構建趨化因子受體(CXCR4)小分子榦擾RNA(siRNA)錶達載體,研究其對體外乳腺癌細胞侵襲能力的影響.方法 選擇CXCR4高錶達的乳腺癌MDA-MB-231細胞繫,設計閤成人CXCR4基因不同靶點的能編碼siRNA的2條雙鏈DNA序列,剋隆到真覈錶達載體pGE-1-U6/kna中構建siRNA錶達載體,體外脂質體介導轉染MDA-MB-231細胞,用Western blot分析CXCR4蛋白錶達,Transwell小室檢測細胞的侵襲能力.結果 成功構建瞭CXCR4-siRNA錶達載體,瞬時轉染乳腺癌細胞後能顯著降低CXCR4的蛋白錶達,可有效抑製人類乳腺癌MDA-MB-231細胞的侵襲能力.結論 CXCR4-siRNA錶達載體通過降低CXCR4基因的蛋白錶達能顯著抑製人類乳腺癌細胞的侵襲能力,有望為乳腺癌轉移的基因治療開闢新途徑.
목적 구건추화인자수체(CXCR4)소분자간우RNA(siRNA)표체재체,연구기대체외유선암세포침습능력적영향.방법 선택CXCR4고표체적유선암MDA-MB-231세포계,설계합성인CXCR4기인불동파점적능편마siRNA적2조쌍련DNA서렬,극륭도진핵표체재체pGE-1-U6/kna중구건siRNA표체재체,체외지질체개도전염MDA-MB-231세포,용Western blot분석CXCR4단백표체,Transwell소실검측세포적침습능력.결과 성공구건료CXCR4-siRNA표체재체,순시전염유선암세포후능현저강저CXCR4적단백표체,가유효억제인류유선암MDA-MB-231세포적침습능력.결론 CXCR4-siRNA표체재체통과강저CXCR4기인적단백표체능현저억제인류유선암세포적침습능력,유망위유선암전이적기인치료개벽신도경.
Objective To construct and identify the siRNA eukaryotic expression vector targeting gene CXC chemo-kine receptor-4 and explore its role in invasion process of breast cancer cells in vitro. Methods Two siRNAs were designed and synthesized according to the coding sequence of CXCR4 gene and cloned into eukaryotic expression plasmid pGE-1-U6/kna. The constructed CXCR4-siRNA expression vector was transfected into MDA-MB-231 cells by liposome. Western blot was used to evaluate the suppression of CXCR4 expression in different groups. The inva-sion and migration of MDA-MB-231 cells were evaluated by cell invasion assay in vitro. Results Enzyme digestion and DNA sequencing confirmed that the CXCR4-siRNA expression vector was successfully constructed. After trans-fection,the CXCR4-siRNA obviously suppressed the expression of CXCR4 compared with control groups and the ability of cell migration was decreased markedly. Conclusion CXCR4-siRNA expression vector can effectively sup-press CXCR4 expression in the breast cancer cells and decrease potential of cell invasion, which may provide a no-vel strategy for gene therapy of breast cancer metastasis.