El-Balat Ahmed, Schmeil Iryna, Karn Thomas, Becker Sven, Sänger Nicole, Holtrich Uwe, Arsenic Ruza
Department of Obstetrics and Gynecology, Goethe University Frankfurt, Theodor-Stern-Kai 7, 60590, Frankfurt, Germany.
Institute of Pathology, Charite University Hospital, Chariteplatz 1, 10117, Berlin, Germany.
Pathol Oncol Res. 2018 Apr;24(2):277-282. doi: 10.1007/s12253-017-0240-4. Epub 2017 May 3.
Borderline tumors (BOT) of the ovary account for 10% to 20% of ovarian neoplasms. Like ovarian cancer, BOT encompass several different histological subtypes (serous, mucinous, endometrioid, clear cell, transitional cell and mixed) with serous (SBOT) and mucinous (MBOT) the most common. Current hypotheses suggest low-grade serous carcinoma may develop in a stepwise fashion from SBOT whereas the majority of high grade serous carcinomas develop rapidly presumably from inclusion cysts or ovarian surface epithelium. The pathogenesis of mucinous ovarian tumors is still puzzling. Molecular markers could help to better define relationships between such entities. Trefoil factor-3 (TFF3) is an estrogen-regulated gene associated with prognosis in different types of cancer. It has also been included in a recent marker panel predicting subtypes of ovarian carcinoma. We analyzed the expression of TFF3 by immunohistochemistry in a cohort of 137 BOT and its association with histopathological features. Overall expression rate of TFF3 was 21.9%. None of the BOT with serous and endometrioid histology displayed strong TFF3 expression. On the other hand, TFF3 was highly expressed in 61.4% of MBOT cases and 33.3% of BOT with mixed histology (P < 0.001) suggesting a potential function of the protein in that subtypes. Associations of TFF3 expression with FIGO stage and micropapillary pattern were significant in the overall cohort but confounded by their correlation with histological subtypes. The highly specific expression of TFF3 in MBOT may help to further clarify potential relationships of tumors with mucinous histology and warrants further studies.
卵巢交界性肿瘤(BOT)占卵巢肿瘤的10%至20%。与卵巢癌一样,BOT包括几种不同的组织学亚型(浆液性、黏液性、子宫内膜样、透明细胞、移行细胞和混合型),其中浆液性(SBOT)和黏液性(MBOT)最为常见。目前的假说认为,低级别浆液性癌可能由SBOT逐步发展而来,而大多数高级别浆液性癌可能迅速由包涵囊肿或卵巢表面上皮发展而来。黏液性卵巢肿瘤的发病机制仍然令人困惑。分子标志物有助于更好地界定这些实体之间的关系。三叶因子-3(TFF3)是一种受雌激素调节的基因,与不同类型癌症的预后相关。它也被纳入最近一个预测卵巢癌亚型的标志物组合中。我们通过免疫组织化学分析了137例BOT队列中TFF3的表达及其与组织病理学特征的关联。TFF3的总体表达率为21.9%。浆液性和子宫内膜样组织学的BOT均未显示TFF3强表达。另一方面,TFF3在61.4%的MBOT病例和33.3%的混合型BOT中高表达(P<0.001),提示该蛋白在该亚型中具有潜在功能。在整个队列中,TFF3表达与国际妇产科联盟(FIGO)分期和微乳头模式的关联显著,但因它们与组织学亚型的相关性而混淆。TFF3在MBOT中的高度特异性表达可能有助于进一步阐明黏液性组织学肿瘤的潜在关系,值得进一步研究。