摘要
目的:探讨IL-2基因转移对卵巢癌细胞系SKOV3致瘤性的影响。方法:通过贴壁集落形成检查、软琼脂集落形成检查和裸鼠皮下成瘤试验,测定IL-2基因转移对卵巢癌细胞系SKOV3致瘤性的影响。结果:SKOV3、SKOV3/Neo和SKOV3/IL-2细胞贴壁集落形成率、软琼脂集落形成率分别为52%、45%、0.7%和31.4%、28.5%、2.4%,SKOV3/IL-2细胞所形成的集落内细胞少,结构松散;裸鼠皮下成瘤实验显示,3组细胞皮下成瘤率分别为100%(12/12)、91.7%(11/12)及56.3%(9/16);成瘤潜伏期平均分别为6.7±0.9d、11.4±4.0d、15.1±6.4d,肿瘤终体积平均分别为1604.3±1469.4mm3、1130.3±1159.7mm3及233.3±126.4mm3;SKOV3/IL-2细胞皮下瘤增殖较SKOV3/Neo和SKOV3细胞明显缓慢(P<0.001)。镜下见SKOV3及SKOV3/Neo组肿瘤呈浸润性生长,并于皮下和肌肉间形成转移病灶,SKOV3/IL-2组肿瘤呈假包膜状生长,瘤内见大量单个核细胞浸润。结论:IL-2基因转移可降低细胞系SKOV3的致瘤?
Objective:To study the effect of IL 2 gene transfer on the tumorigenesis of ovarian cancer cell line SKOV3.Methods:Colony forming examination,soft agar colony forming examination,and subcutaneous tumor forming test in nude mice were used to detect about the mentioned effects.Results:The average colony forming efficiency of SKOV3,SKOV3/Neo and SKOV3/IL 2 cells in colony forming examination and soft agar colony forming examination were 52%,45%,0.7% and 31.4%,28.5%,2.4% respectively.The average latency and tumorigenesis of subcutaneous tumor forming in nude mice were 6.7±0.9d,11.4±4.0d,15.1±6.4d and 100%(12/12),91.7%(11/12),56.3%(9/16)respectively.The average end tumor volumes were 1604.3±1469.4mm 3,1130.3±1159.7 mm 3 and 233.3±126.4mm 3 respectively,SKOV3/IL 2 grew more slowly than that in the control group.Histologic study demonstrated that SKOV3 and SKOV3/Neo were more aggressive than SKOV3/IL 2 cells and invasive focuses were formed.There was large amount of mononuclear cells infiltrated into the tumor of SKOV3/IL 2 cells.Conclusion:hIL 2 gene modification can reduce the tumorigenesis of ovarian cancer cell line SKOV3 and induce the infiltration of mononuclear cells into the subcutaneous tumor of nude mice.
出处
《现代妇产科进展》
CSCD
1998年第2期122-126,共5页
Progress in Obstetrics and Gynecology