中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2008年
12期
1649-1651
,共3页
吴兴%楼列名%陈峥嵘%张光健
吳興%樓列名%陳崢嶸%張光健
오흥%루렬명%진쟁영%장광건
环氧合酶.2%骨肉瘤%侵袭%反义寡核苷酸类
環氧閤酶.2%骨肉瘤%侵襲%反義寡覈苷痠類
배양합매.2%골육류%침습%반의과핵감산류
Cyclooxygenase-2%Osteosarcoma%Invasion%Antisense oligodeoxynueleotides
目的 探讨环氧合酶-2(COX-2)反义寡核苷酸(ODNs)对人骨肉瘤细胞株OS-732侵袭性的抑制作用及其机制.方法 设计和合成COX-2反义寡核苷酸,体外转染骨肉瘤OS-732细胞,逆转录.聚合酶链反应(RT-PCR)及Western blot证实转染效果.改良Boyden-transwell方法观察肿瘤细胞侵袋抑制率,RT-PCR方法研究转染COX-2反义ODNs对OS-732细胞尿激酶型纤溶酶原激活物及其受体(uPA、uPAR)mRNA表达的影响.结果 转染COX-2反义ODNs的细胞COX-2核酸、蛋白表达水平显著降低.转染组细胞侵袭能力显著降低,呈浓度依赖性.转染组细胞uPA、uPAR的mRNA表达水平显著降低(P<0.01).结论 COX-2反义ODNs对OS-732细胞侵袭能力有明显抑制作用,其对uPA、uPAR表达的下调是主要作用机制.
目的 探討環氧閤酶-2(COX-2)反義寡覈苷痠(ODNs)對人骨肉瘤細胞株OS-732侵襲性的抑製作用及其機製.方法 設計和閤成COX-2反義寡覈苷痠,體外轉染骨肉瘤OS-732細胞,逆轉錄.聚閤酶鏈反應(RT-PCR)及Western blot證實轉染效果.改良Boyden-transwell方法觀察腫瘤細胞侵袋抑製率,RT-PCR方法研究轉染COX-2反義ODNs對OS-732細胞尿激酶型纖溶酶原激活物及其受體(uPA、uPAR)mRNA錶達的影響.結果 轉染COX-2反義ODNs的細胞COX-2覈痠、蛋白錶達水平顯著降低.轉染組細胞侵襲能力顯著降低,呈濃度依賴性.轉染組細胞uPA、uPAR的mRNA錶達水平顯著降低(P<0.01).結論 COX-2反義ODNs對OS-732細胞侵襲能力有明顯抑製作用,其對uPA、uPAR錶達的下調是主要作用機製.
목적 탐토배양합매-2(COX-2)반의과핵감산(ODNs)대인골육류세포주OS-732침습성적억제작용급기궤제.방법 설계화합성COX-2반의과핵감산,체외전염골육류OS-732세포,역전록.취합매련반응(RT-PCR)급Western blot증실전염효과.개량Boyden-transwell방법관찰종류세포침대억제솔,RT-PCR방법연구전염COX-2반의ODNs대OS-732세포뇨격매형섬용매원격활물급기수체(uPA、uPAR)mRNA표체적영향.결과 전염COX-2반의ODNs적세포COX-2핵산、단백표체수평현저강저.전염조세포침습능력현저강저,정농도의뢰성.전염조세포uPA、uPAR적mRNA표체수평현저강저(P<0.01).결론 COX-2반의ODNs대OS-732세포침습능력유명현억제작용,기대uPA、uPAR표체적하조시주요작용궤제.
Objective To investigate the inhibitory effects of cyclooxygenase-2 (COX-2) antisense oligodeoxynucleotides (anti-ODNs) on the invasion of osteosarcoma OS-732 cell line and the mechanism. Methods The COX-2 anti-ODNs were designed,synthesized and transfected into OS-732 cell line. The transfection effects were confrimed by RT-PCR and Western blot. The invasion inhibition ratio of OS732 cells was detected by modified Boyden-transwell techniques. The effects of COX-2 anti-ODNs on mRNA expression of uPA and uPAR were studied by RT-PCR. Results The expression of COX-2 mRNA and protein was decreased after transfecting COX-2 anti-ODNs into OS-732 cell line in a certain degree of dose-dependent manner. The expression of uPA and uPAR mRNA in transfected OS-732 cells were notably decreased by RT-PCR compared with control groups. Conclusion COX-2 anti-ODNs could remarkably inhibit the invasion ability of OS-732 cells probably by down-regulating the expression of uPA and uPAR.