中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2013年
8期
1659-1661,封3-封4
,共4页
谢忆山%伍龙%刘少平%彭春伟%李雁
謝憶山%伍龍%劉少平%彭春偉%李雁
사억산%오룡%류소평%팽춘위%리안
胃癌%基因治疗%p53%肝脏不良反应
胃癌%基因治療%p53%肝髒不良反應
위암%기인치료%p53%간장불량반응
Gastric cancer%Gene therapy%p53%Liver toxicity
目的 探讨重组人腺病毒p53(rAd-p53)对胃癌细胞裸鼠移植瘤的抗肿瘤效应及相关不良反应.方法 将胃癌细胞SGC-7901注射于裸鼠皮下制成动物模型,分别用rAd-p53和盐酸表阿霉素(EPI)进行治疗.rAd-p53治疗组剂量为10μl浓度1012vp/ml,EPI治疗组剂量为1.25mg/kg,各组每3周给药7次,以生理盐水为对照组.结果 与对照组比较,rAd-p53治疗组和EPI治疗组肿瘤抑制率分别为80%和60%,差异有统计学意义(P<0.01);rAd-p53和EPI治疗组之间比较差异无统计学意义(P>0.05).没有实验动物死亡,rAd-p53治疗组2只裸鼠出现肝脏不良反应,EPI治疗组1只裸鼠心脏不良反应,上述反应均有病理学观察证实.结论 裸鼠体内实验证实rAd-p53对胃癌细胞具有抗肿瘤效应,但应注意其肝脏不良反应.
目的 探討重組人腺病毒p53(rAd-p53)對胃癌細胞裸鼠移植瘤的抗腫瘤效應及相關不良反應.方法 將胃癌細胞SGC-7901註射于裸鼠皮下製成動物模型,分彆用rAd-p53和鹽痠錶阿黴素(EPI)進行治療.rAd-p53治療組劑量為10μl濃度1012vp/ml,EPI治療組劑量為1.25mg/kg,各組每3週給藥7次,以生理鹽水為對照組.結果 與對照組比較,rAd-p53治療組和EPI治療組腫瘤抑製率分彆為80%和60%,差異有統計學意義(P<0.01);rAd-p53和EPI治療組之間比較差異無統計學意義(P>0.05).沒有實驗動物死亡,rAd-p53治療組2隻裸鼠齣現肝髒不良反應,EPI治療組1隻裸鼠心髒不良反應,上述反應均有病理學觀察證實.結論 裸鼠體內實驗證實rAd-p53對胃癌細胞具有抗腫瘤效應,但應註意其肝髒不良反應.
목적 탐토중조인선병독p53(rAd-p53)대위암세포라서이식류적항종류효응급상관불량반응.방법 장위암세포SGC-7901주사우라서피하제성동물모형,분별용rAd-p53화염산표아매소(EPI)진행치료.rAd-p53치료조제량위10μl농도1012vp/ml,EPI치료조제량위1.25mg/kg,각조매3주급약7차,이생리염수위대조조.결과 여대조조비교,rAd-p53치료조화EPI치료조종류억제솔분별위80%화60%,차이유통계학의의(P<0.01);rAd-p53화EPI치료조지간비교차이무통계학의의(P>0.05).몰유실험동물사망,rAd-p53치료조2지라서출현간장불량반응,EPI치료조1지라서심장불량반응,상술반응균유병이학관찰증실.결론 라서체내실험증실rAd-p53대위암세포구유항종류효응,단응주의기간장불량반응.
Objective To investigate the inhibitory and side effects of recombinant Adenoviruswtp53 (tAd-p53) SGC-7901 on gastric cancer cells in vivo.Methods SGC-7901 cells were subcutaneously injected into the nude mice to establish xenograph models,which were treated with Gendicine,a recombinant human Ad-p53 injection (rAd-p53),and epirubicin hydrochloride (EPI),a cytotoxic chemotherapy agent.Results As compared with the blank control,treatment with rAd-p53 at the dose of 10 μl of 1012 vp/ml and EPI at the dose of 1.25 mg/kg,7 times every 3 weeks,resulted in 80% and 60% of tumor growth inhibition,respectively.The difference in rAd-p53 and EPI therapy group was not statistically significant.No animal death was observed,although 2 nude mice in rAd-p53 group developed liver toxicity and 1 nude mouse in EPI group developed cardiac toxicity,and the results were validated histopathologically.Conclusion The rAd-p53 has tumor inhibitory effect on gastric cancer cells,but the liver toxicity should be considered seriously.