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拓扑异构酶IIα表达与妇科恶性肿瘤中拓扑异构酶II靶向药物化疗敏感性检测的相关性

Correlation between Topo II alpha expression and chemosensitivity testing for Topo II-targeting drugs in gynaecological carcinomas.

作者信息

Koshiyama M, Fujii H, Kinezaki M, Yoshida M

机构信息

Department of Obstetrics and Gynaecology, Tenri Hospital, Tenri, Nara, Japan.

出版信息

Anticancer Res. 2001 Mar-Apr;21(2A):905-10.

PMID:11396183
Abstract

BACKGROUND

The purpose of this study was to investigate the correlation between topoisomerase II alpha (Topo II alpha) expression and the chemosensitivity to Topo II-targeting drugs in gynaecological carcinomas.

MATERIALS AND METHODS

We analysed the expression of Topo II alpha, and then correlated this with the in vitro chemosensitivities of 43 gynaecological tumors using immunohistochemistry and a tetrazolium dye (MTT) assay.

RESULTS

There was a significant correlation between the Topo II alpha index (the number of positive cells per 100 cells: %) and the tumor cell growth inhibition rate in culture (I.R.: %) for doxorubicin and etoposide (r = 0.631, p < 0.001 and r = 0.645, p < 0.001, respectively). The I.Rs for doxorubicin and etoposide in endometrial carcinomas were lower than those in ovarian carcinomas [38.2 +/- 22.8 vs 54.6 +/- 29.8, 37.3 +/- 19.8 vs 59.3 +/- 30.6] (p < 0.05, respectively). Furthermore, the number of high Topo II alpha index (over 30%) tumors in the ovarian carcinoma cases was higher than that in the endometrial carcinoma cases (63.1% vs 45.8%, p < 0.05).

CONCLUSIONS

Our data suggest that the Topo II alpha index of a tumor is a reflection of its chemosensitivity to Topo II-targeting drugs. The use of this index may enable prediction of a clinical response to chemotherapy using Topo II-targeting drugs in gynaecological malignancies.

摘要

背景

本研究旨在探讨拓扑异构酶IIα(Topo IIα)表达与妇科恶性肿瘤对拓扑异构酶II靶向药物的化疗敏感性之间的相关性。

材料与方法

我们分析了Topo IIα的表达情况,然后通过免疫组织化学和四氮唑盐(MTT)法将其与43例妇科肿瘤的体外化疗敏感性进行关联分析。

结果

对于阿霉素和依托泊苷,Topo IIα指数(每100个细胞中的阳性细胞数:%)与培养中的肿瘤细胞生长抑制率(I.R.:%)之间存在显著相关性(分别为r = 0.631,p < 0.001和r = 0.645,p < 0.001)。子宫内膜癌中阿霉素和依托泊苷的I.R.低于卵巢癌[38.2±22.8对54.6±29.8,37.3±19.8对59.3±30.6](p均<0.05)。此外,卵巢癌病例中Topo IIα指数高(超过30%)的肿瘤数量高于子宫内膜癌病例(63.1%对45.8%,p < 0.05)。

结论

我们的数据表明肿瘤的Topo IIα指数反映了其对拓扑异构酶II靶向药物的化疗敏感性。使用该指数可能有助于预测妇科恶性肿瘤中使用拓扑异构酶II靶向药物化疗的临床反应。

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