Fadare Oluwole, Zheng Wenxin
Department of Pathology, Wilford Hall Medical Center, Lackland Air Force Base San Antonio, Texas, USA.
Int J Clin Exp Pathol. 2009;2(5):411-32. Epub 2009 Jan 10.
Endometrial serous carcinomas (ESC) constitute only approximately 10% of endometrial cancers, but have a substantially higher case-fatality rate than their more common endometrioid counterparts. The precise composite of factors driving endometrial serous carcinogenesis and progression remain largely unknown, but we attempt to review the current state of knowledge in this report. ESC probably do not evolve through a single pathway, and their underlying molecular events probably occur early in their evolution. TP53 gene mutations occur in 22.7 to 96% of cases, and p53 protein overexpression is seen in approximately 76%. By gene expression profiling, p16 is upregulated in ESC significantly above both normal endometrial cells and endometrioid carcinomas, and 92-100% of cases display diffuse expression of the p16 protein by immunohistochemistry (IHC). Together, these findings suggest dysregulation of both the p16(INKA)/Cyclin D-CDK/pRb-E2F and the ARF-MDM2-p53 cell cycle pathways in ESC. By IHC, HER2/neu is overexpressed (2+ or 3+) in approximately 32.1% of ESC, and approximately 54.5% of cases scored as 2+ or 3+ by IHC display c-erbB2 gene amplification as assessed by fluorescent in situ hybridization. Genetic instability, typically manifested as loss of heterozygosity in multiple chromosomes, is a common feature of ESC, and one study found loss of heterozygosity at 1p32-33 in 63% of cases. A subset of ESC display protein expression patterns that are characteristic of high grade endometrial carcinomas, including loss of the metastasis suppressor CD82 (KAI-1) and epithelial-to-mesenchymal transformation, the latter manifested as E-cadherin downregulation, P-cadherin upregulation, and expression of epithelial-to-mesenchymal transformation-related molecules such as zinc-finger E-box-binding homeobox 1 (ZEB1) and focal adhesion kinase. Preliminary data suggests differential patterns of expression in ESC of some isoforms of claudins, proteases, the tumor invasiveness and progression-associated oncofetal protein insulin-like growth factor II mRNA-binding protein 3 (IMP3), as well as a variety of other molecules. At the morphologic level, evidence that indicates that endometrial glandular dysplasia (EmGD) is the most likely morphologically recognizable precursor lesion to ESC is presented. We advocate use of the term endometrial intraepithelial carcinoma (EIC, or its other appellations) only as a morphologic descriptor and never as a diagnostic/pathologic statement of biologic potential. Given its potential for extrauterine extension, we consider the lesions described as EIC, when present in isolation, as examples of localized ESC, and patients should be managed as such. Morphologically normal, p53 immunoreactive endometrial cells (the so-called "p53 signatures"), show a statistically significant association with ESC, display p53 mutations in a significant subset, and form the start of a progression model, outlined herein, from p53 signatures to EmGD to localized ESC to the more conventionally invasive neoplasm. The identification of a morphologically-recognizable precursor holds the promise of early detection of ESC, with the attendant reduction in its overall associated mortality rate. Deciphering the molecular basis for endometrial serous carcinogenesis should uncover potential targets for diagnosis, therapy, and/or disease surveillance.
子宫内膜浆液性癌(ESC)仅占子宫内膜癌的约10%,但其病死率远高于更为常见的子宫内膜样癌。驱动子宫内膜浆液性癌发生和进展的精确综合因素仍大多未知,但我们试图在本报告中综述当前的知识状况。ESC可能并非通过单一途径演变,其潜在的分子事件可能在其演变早期就已发生。TP53基因突变在22.7%至96%的病例中出现,p53蛋白过表达在约76%的病例中可见。通过基因表达谱分析,p16在ESC中的上调显著高于正常子宫内膜细胞和子宫内膜样癌,并且92%至100%的病例通过免疫组织化学(IHC)显示p16蛋白弥漫性表达。这些发现共同提示ESC中p16(INKA)/细胞周期蛋白D - 细胞周期蛋白依赖性激酶/pRb - E2F和ARF - MDM2 - p53细胞周期途径均失调。通过IHC,HER2/neu在约32.1%的ESC中过表达(2+或3+),并且通过荧光原位杂交评估,约54.5% IHC评分为2+或3+的病例显示c - erbB2基因扩增。基因不稳定,通常表现为多条染色体杂合性缺失,是ESC的一个常见特征,一项研究发现63%的病例在1p32 - 33处存在杂合性缺失。一部分ESC表现出高级别子宫内膜癌的特征性蛋白表达模式,包括转移抑制因子CD82(KAI - 1)缺失和上皮 - 间质转化,后者表现为E - 钙黏蛋白下调、P - 钙黏蛋白上调以及上皮 - 间质转化相关分子如锌指E盒结合同源框1(ZEB1)和粘着斑激酶的表达。初步数据表明,紧密连接蛋白、蛋白酶、肿瘤侵袭和进展相关的癌胚蛋白胰岛素样生长因子II mRNA结合蛋白3(IMP3)以及多种其他分子的某些亚型在ESC中的表达模式存在差异。在形态学层面,有证据表明子宫内膜腺体发育异常(EmGD)是ESC最有可能在形态学上可识别的前驱病变。我们主张仅将子宫内膜上皮内癌(EIC,或其其他名称)用作形态学描述符,而绝不用作生物学潜能的诊断/病理表述。鉴于其宫外扩展的可能性,我们认为单独存在时被描述为EIC的病变是局限性ESC的例子,患者应按此进行管理。形态学正常的p53免疫反应性子宫内膜细胞(所谓的“p53特征”)与ESC存在统计学上的显著关联,在相当一部分中显示p53突变,并形成了本文概述的从p53特征到EmGD到局限性ESC再到更具传统侵袭性肿瘤的进展模型。识别出形态学上可识别的前驱病变有望实现ESC的早期检测,随之降低其总体相关死亡率。解读子宫内膜浆液性癌发生的分子基础应能揭示诊断、治疗和/或疾病监测的潜在靶点。