Department of Surgery, National University of Ireland, Galway, Clinical Science Institute, Costello Road, Galway, Ireland.
Ann Surg Oncol. 2010 May;17(5):1392-7. doi: 10.1245/s10434-009-0855-0. Epub 2010 Mar 9.
Many patients with breast cancer receive no benefit from their treatment. This has led to a search for novel therapeutic targets whose identification may facilitate a more tailored approach, thereby avoiding unnecessary toxicity. Of these, topoisomerase 2 alpha (TOP2A), located at the HER2/neu amplicon on chromosome 17, has generated particular interest because its expression has been shown to correlate with response to anthracycline-based therapies.
We evaluated the relationship between TOP2A and its collocated gene, HER2/neu, and summarized the evidence for and against confining anthracycline-based therapies to those patients who demonstrate increased expression or amplification of these targets.
The emerging consensus supports the restriction of anthracyclines to those patients who are HER2/neu positive, with the evidence suggesting that alterations in the status of TOP2A are almost completely restricted to this group of patients.
It seems increasingly likely that response to anthracyclines is predicated on these alterations.
许多乳腺癌患者的治疗没有获益。这促使人们寻找新的治疗靶点,其鉴定可能有助于更有针对性的治疗方法,从而避免不必要的毒性。其中,拓扑异构酶 2α(TOP2A)位于染色体 17 上的 HER2/neu 扩增子上,因其表达与蒽环类药物治疗的反应相关而引起了特别的关注。
我们评估了 TOP2A 与其相邻基因 HER2/neu 之间的关系,并总结了支持和反对将蒽环类药物限于表达或扩增这些靶点的患者的证据。
新出现的共识支持将蒽环类药物限于 HER2/neu 阳性的患者,证据表明,TOP2A 状态的改变几乎完全限于这组患者。
蒽环类药物的反应似乎越来越取决于这些改变。