Functional Genomics of Ovarian Cancer Laboratory, Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Robinson Way, Cambridge, UK.
J Pathol. 2011 Oct;225(2):157-60. doi: 10.1002/path.2970.
It has become increasingly clear that the four main histological subtypes of epithelial ovarian cancer (EOC), high-grade serous, endometrioid, clear cell and mucinous, are entities with different epidemiologies, clinical presentations, responses to treatment, and ultimate outcomes. In fact, for all intents and purposes, they can be considered different diseases, their only common denominator being that they frequently involve the ovary and pelvic organs. However, clinical practice has not caught up with these insights and the treatment of EOC is that of a single disease entity. In part, this is because we lack detailed knowledge of the molecular mechanisms driving the pathogenesis of each disease, which is vital in order to develop therapeutic approaches against common driver events. In the last few years, mutations in ARID1A and PIK3CA have been described in a substantial fraction of cases of ovarian clear cell carcinoma, yet the paper by Yamamoto et al in this issue of The Journal of Pathology reveals that PIK3CA mutations can be detected in precursor endometriosis tissues. These and other recent observations underscore the importance of investigating whether mutations in the eutopic endometrium actually predispose to endometriosis and eventually to malignancy.
越来越明显的是,卵巢上皮癌(EOC)的四种主要组织学亚型——高级别浆液性、子宫内膜样、透明细胞和黏液性——是具有不同流行病学、临床表现、治疗反应和最终结局的实体。事实上,从所有意图和目的来看,它们可以被认为是不同的疾病,它们唯一的共同点是它们经常涉及卵巢和盆腔器官。然而,临床实践并没有跟上这些新的认识,EOC 的治疗仍然被视为一种单一的疾病实体。部分原因是我们缺乏对每种疾病发病机制的分子机制的详细了解,而这对于开发针对常见驱动事件的治疗方法至关重要。在过去的几年中,ARID1A 和 PIK3CA 的突变已在大量卵巢透明细胞癌病例中被描述,但 Yamamoto 等人在本期《病理学杂志》上的论文表明,PIK3CA 突变可在子宫内膜异位症的前驱组织中检测到。这些和其他最近的观察结果强调了研究内异症和恶性肿瘤中是否存在腔上皮细胞突变是否会导致易感性的重要性。