摘要
目的探讨Tat(transactivator of transcription)结合蛋白30(Tat-interactive protein 30,TIP30)在脑星形细胞瘤发生发展中的作用。方法采用免疫组化链霉菌抗生物素蛋白过氧化酶法(SP)和末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)分别检测69例脑星形细胞瘤和8例正常脑组织中TIP30蛋白表达、增殖细胞核抗原标记指数(PCNA LI)、微血管密度(MVD)和瘤细胞的凋亡指数(AI)。结果 69例脑星形细胞瘤组织TIP30的阳性表达率为49.3%,明显低于正常脑组织100%(P<0.01);TIP30的阳性表达率随星形细胞瘤的病理分级级别的升高而降低(χ2=16.31,P<0.01);TIP30蛋白阳性表达的星形细胞瘤组织中的MVD值(30.08±5.63)和PCNA LI值(22.29±7.15)明显低于TIP30蛋白阴性组的MVD值(47.83±8.27)和PCNA LI值(48.11±7.16)(P均<0.01);TIP30蛋白阳性表达的星形细胞瘤组织中的AI值(6.66±1.03)明显高于TIP30蛋白阴性组的AI值(4.02±1.09)(P<0.01)。结论星形细胞瘤中TIP30蛋白表达下降,可能是通过促进新生血管形成、瘤细胞增生和抑制凋亡作用参与了脑星形细胞瘤的发生发展过程。
Objective To explore putative roles of transactivator of transcricption-interactive protein 30(TIP30) in the initiation and progression of astrocytoma.Methods The expression of TIP30,proliferating cell nuclear antigen labeling index(PCNALI),microvascular density(MVD),apoptosis index(AI) in 69 cases of astrocytomas and 8 cases of normal brain tissue were comparatively studied with immunohistochemical staining method and termindal deoxynucleotidyl transfernase-mediated nick end labeling(TUNEL).Results The expression of TIP30 in astrocytoma was lower than that of normal brain tissue and was negatively related to the histological grade of tumor(χ2=16.31,P〈0.01).MVD and PCNALI with positive expression of TIP30 in astrocytoma were significantly lower than that with negative expression(P〈0.01,P〈0.01).AI with positive expression of TIP30 in astrocytoma was significantly higher than that with negative expression(P〈0.01).Conclusion The decrease in expression of TIP30 may play an important role in the initiation and progression of astrocytoma by promoting angiogenesis,tumor cell hyperplasia and decreasing apoptosis.
出处
《中国公共卫生》
CAS
CSCD
北大核心
2010年第9期1164-1165,共2页
Chinese Journal of Public Health
基金
河北省2007年医学科学研究重点课题计划项目(07321)