McLeod H L, Douglas F, Oates M, Symonds R P, Prakash D, van der Zee A G, Kaye S B, Brown R, Keith W N
CRC Department of Medical Oncology, University of Glasgow, The Netherlands.
Int J Cancer. 1994 Dec 1;59(5):607-11. doi: 10.1002/ijc.2910590506.
The identification of human DNA topoisomerases as cellular targets for active anti-cancer drugs has stimulated further interest in topoisomerase function in tumour biology. Topoisomerase I and II catalytic activity is detectable in many normal and malignant tissues. However, little is known about the expression of topoisomerases in most human solid tumours. The present study evaluated topoisomerase I and II activity in biopsy samples from 86 patients with breast, lung, cervix or colon cancers. Significant intra- and inter-tumour variation in topoisomerase expression was observed. Topoisomerase I activity was relatively high in cervix and colon tumours in comparison to lung and breast cancers. Topoisomerase II activity was high in cervix, colon and lung cancers relative to breast cancer. Topoisomerase I and II activity co-segregated in individual colon tumour samples, but no correlation was observed in cervix, lung or breast tumours. The large heterogeneity in both topoisomerase I and II activity within a tumour type suggests a mechanism for variable response to topoisomerase-directed therapy. The differences in activity between tumour groups suggest that the potential efficacy of inhibitors of topoisomerase I in colon and cervical tumours may be greater than in lung and breast tumours. Future in vivo evaluation is required to establish the clinical relevance of the observed heterogeneity in topoisomerase activity.
将人类DNA拓扑异构酶鉴定为活性抗癌药物的细胞靶点,激发了人们对拓扑异构酶在肿瘤生物学中功能的进一步兴趣。拓扑异构酶I和II的催化活性在许多正常组织和恶性组织中都可检测到。然而,对于大多数人类实体瘤中拓扑异构酶的表达情况,人们了解甚少。本研究评估了86例乳腺癌、肺癌、宫颈癌或结肠癌患者活检样本中的拓扑异构酶I和II活性。观察到肿瘤内和肿瘤间拓扑异构酶表达存在显著差异。与肺癌和乳腺癌相比,宫颈癌和结肠癌中拓扑异构酶I活性相对较高。与乳腺癌相比,宫颈癌、结肠癌和肺癌中拓扑异构酶II活性较高。在单个结肠肿瘤样本中,拓扑异构酶I和II活性共同分离,但在宫颈癌、肺癌或乳腺癌中未观察到相关性。肿瘤类型内拓扑异构酶I和II活性的巨大异质性提示了对拓扑异构酶导向治疗反应可变的一种机制。肿瘤组之间活性的差异表明,拓扑异构酶I抑制剂在结肠癌和宫颈癌中的潜在疗效可能大于在肺癌和乳腺癌中的疗效。需要进行进一步的体内评估,以确定所观察到的拓扑异构酶活性异质性的临床相关性。