Zhao H, Yu H, Liu Y, Wang Y, Cai W
Department of Neurosurgery, The Second Affiliated Hospital (Shengjing Hospital), China Medical University, Heping District, Shenyang, China.
Clin Neuropathol. 2008 Mar-Apr;27(2):83-90. doi: 10.5414/npp27083.
DNA topoisomerase II-alpha (Topo-IIalpha) is the inducible form of the enzyme responsible for the first step in the modification of DNA topology. Topo-IIalpha upregulation has been demonstrated in different tumors. Topo-IIalpha products may modulate tumoral growth, metastasis and immunosuppression, inhibit apoptosis and cause resistance to chemotherapy. Moreover, the antitumoral effect ofTopo-IIalpha inhibitors has been documented.
We studied the immunohistochemical expression and the prognostic value of Topo-IIalpha on 57 surgical specimens ofglioma. Furthermore, we evaluated the correlation between the immunohistochemical expression of Topo-IIalpha and proliferating cell nuclear antigen (PCNA).
A statistically significant correlation with survival time was found, there was no statistically significant difference in survival between patients receiving or not receiving carmustine-based combined chemotherapy (p > 0.05), regardless of histological type. A significant correlation between Topo-IIalpha and PCNA was documented (r = 0.9245, p < 0.001).
Our findings show that gliomas immunohistochemically express Topo-IIalpha that is correlated with PCNA expression, and which is significantly less frequent in long survivors. The presence of a statistical correlation with survival time and tumor histological grade encourages further studies on a larger series to verify the prognostic value of Topo-IIalpha expression in gliomas.
DNA拓扑异构酶II-α(Topo-IIα)是负责DNA拓扑结构改变第一步的可诱导型酶。Topo-IIα上调已在不同肿瘤中得到证实。Topo-IIα产物可能调节肿瘤生长、转移和免疫抑制,抑制细胞凋亡并导致化疗耐药。此外,Topo-IIα抑制剂的抗肿瘤作用也已得到记载。
我们研究了57例神经胶质瘤手术标本中Topo-IIα的免疫组化表达及其预后价值。此外,我们评估了Topo-IIα免疫组化表达与增殖细胞核抗原(PCNA)之间的相关性。
发现与生存时间存在统计学显著相关性,无论组织学类型如何,接受或未接受卡莫司汀联合化疗的患者生存率无统计学显著差异(p>0.05)。记录到Topo-IIα与PCNA之间存在显著相关性(r=0.9245,p<0.001)。
我们的研究结果表明,神经胶质瘤免疫组化表达Topo-IIα,其与PCNA表达相关,且在长期存活者中出现频率显著较低。与生存时间和肿瘤组织学分级存在统计学相关性,这鼓励对更大样本系列进行进一步研究,以验证Topo-IIα表达在神经胶质瘤中的预后价值。