肿瘤研究与临床
腫瘤研究與臨床
종류연구여림상
CANCER RESEARCH AND CLINIC
2010年
2期
101-104
,共4页
杨强%邓志华%刘燕%贾静%郭素雅%刘京龙
楊彊%鄧誌華%劉燕%賈靜%郭素雅%劉京龍
양강%산지화%류연%가정%곽소아%류경룡
肝肿瘤%实验性%基因疗法%胸苷激酶%腺病毒%人%腹腔积液
肝腫瘤%實驗性%基因療法%胸苷激酶%腺病毒%人%腹腔積液
간종류%실험성%기인요법%흉감격매%선병독%인%복강적액
Liver neoplasms,experimental%Gene therapy%Kinase adenosine%Adenoviruses.human%Ascites
目的 研究重组腺病毒Ad-hTERTp-HSV-TK/GCV系统对小鼠肝癌腹腔种植腹腔积液生成的影响及其作用机制.方法 sx_1,近交系小鼠腹腔内接种肝癌H22细胞株后,随机分为四组,48 h后分别给予相应的治疗.观察各组小鼠腹腔积液及生存时间的变化;流式细胞术测定肿瘤细胞凋亡百分率;透射电镜观察腹腔内肿瘤细胞的形态学变化.结果 与Ad-hTERTp-HSV-TK组、GCV组和空白对照组三组相比,Ad-hTERTp-HSV-TK/GCV组可以显著抑制小鼠腹腔积液的生成(P<0.01),延长生存期(P<0.01),肿瘤细胞凋亡率为(27.12±2.12)%明显高于其他各组(P<0.01),并且在治疗期间未发现明显不良反应.结论 Ad-hTERTp-HSV-TK/GCV系统可通过诱导肝癌细胞凋亡而抑制小鼠腹腔积液生成,并延长生存期,是一种安全可行的治疗方法.
目的 研究重組腺病毒Ad-hTERTp-HSV-TK/GCV繫統對小鼠肝癌腹腔種植腹腔積液生成的影響及其作用機製.方法 sx_1,近交繫小鼠腹腔內接種肝癌H22細胞株後,隨機分為四組,48 h後分彆給予相應的治療.觀察各組小鼠腹腔積液及生存時間的變化;流式細胞術測定腫瘤細胞凋亡百分率;透射電鏡觀察腹腔內腫瘤細胞的形態學變化.結果 與Ad-hTERTp-HSV-TK組、GCV組和空白對照組三組相比,Ad-hTERTp-HSV-TK/GCV組可以顯著抑製小鼠腹腔積液的生成(P<0.01),延長生存期(P<0.01),腫瘤細胞凋亡率為(27.12±2.12)%明顯高于其他各組(P<0.01),併且在治療期間未髮現明顯不良反應.結論 Ad-hTERTp-HSV-TK/GCV繫統可通過誘導肝癌細胞凋亡而抑製小鼠腹腔積液生成,併延長生存期,是一種安全可行的治療方法.
목적 연구중조선병독Ad-hTERTp-HSV-TK/GCV계통대소서간암복강충식복강적액생성적영향급기작용궤제.방법 sx_1,근교계소서복강내접충간암H22세포주후,수궤분위사조,48 h후분별급여상응적치료.관찰각조소서복강적액급생존시간적변화;류식세포술측정종류세포조망백분솔;투사전경관찰복강내종류세포적형태학변화.결과 여Ad-hTERTp-HSV-TK조、GCV조화공백대조조삼조상비,Ad-hTERTp-HSV-TK/GCV조가이현저억제소서복강적액적생성(P<0.01),연장생존기(P<0.01),종류세포조망솔위(27.12±2.12)%명현고우기타각조(P<0.01),병차재치료기간미발현명현불량반응.결론 Ad-hTERTp-HSV-TK/GCV계통가통과유도간암세포조망이억제소서복강적액생성,병연장생존기,시일충안전가행적치료방법.
Objective To observe the effect of Ad-bTERTp-HSV-TK/GCV system on malignant ascites of mice and probe into its mechanism of action.Methods The SX1 inbred strain mice were injected with H22 cell line of liver cancer and were divided into 4 groups at random.The mice in each group were given corresponding treatment after 48 hours.The production of ascites and survival period were evaluated. The apoptosis rates of tumor cells were detected by FCM.Morphological changes of tumor cells were studied by electromicroscope.Results Compared with other groups.Ad-hTERTp-HSV-TK/GCV Can obviously inhibit the production of ascites(P<0.01),prolong the survival period (P<0.01),and apoptosis rate in this group (27.12±2.12)% was significantly higher than that in other groups.No obvious side effect Was found during the treatment.Conclusion Ad-hTERTp-HSV-TK/GCV system Can inhibit production of ascites and prolong the survical period of mice by inducing apoptosis of hepatoma cells,which is a safe and feasible treatment for hepatoma therapy.