Yang Qin, Jiang Wei, Li Lei, Huang Qin, Yang Kai-xuan
Department of Anatomy and Histology, Chengdu Medical College, 610083, Chengdu, Sichuan Province, People's Republic of China.
Department of Pathology, West China Second University Hospital, Sichuan University, 610041, Chengdu, Sichuan Province, People's Republic of China.
Ann Diagn Pathol. 2014 Aug;18(4):232-7. doi: 10.1016/j.anndiagpath.2014.04.003. Epub 2014 May 6.
Mucinous minimal deviation adenocarcinoma (MDA) is a rare highly differentiated tumor of uterine cervix, of which the confusing histopathology resembling some benign lesions usually makes difficulty for pathologic diagnosis. The expression of forkhead box protein P1 (FOXP1) is found in some kinds of human tumors and is considered to be associated with the progression of the tumors. The purpose of this study is to detect the FOXP1 expression in MDA and evaluate its possible role in the diagnosis of MDA. Twenty-two MDA cases and 20 control cases consisting of 10 cases of lobular endocervical glandular hyperplasia and 10 cases of normal endocervical tissue were included in this study. All available clinical data were collected and immunostaining for FOXP1, carcinoembryonic antigen (CEA), human milk fat globule antigen 1 (HMFG1), estrogen receptor, and progesterone receptor were performed on these cases. The nuclear/cytoplasmic expression of FOXP1 was found in 18 of 22 MDA cases while in 1 of 20 control cases, which showed statistical significance (P = .000). The cytoplasmic CEA expression was found in 14 of 22 MDA cases and 2 of 20 control cases (P = .000), whereas cytoplasmic HMFG1 expression was found in 10 of 22 MDA cases and 4 of 20 control cases (P = .081). No statistical difference was found between FOXP1 and CEA expression (P = .083) or between FOXP1 and HMFG1 expression (P = .375) in MDA. Neither estrogen receptor nor PR expression was found in MDA. The significant expression of FOXP1 in MDA may be helpful to some extent in the pathologic diagnosis of cervical MDA. A widened observation range and further researches are needed to elucidate the potential mechanism.
黏液性微偏腺癌(MDA)是一种罕见的子宫颈高分化肿瘤,其组织病理学表现易与一些良性病变混淆,常给病理诊断带来困难。叉头框蛋白P1(FOXP1)在某些人类肿瘤中表达,被认为与肿瘤进展相关。本研究旨在检测MDA中FOXP1的表达,并评估其在MDA诊断中的可能作用。本研究纳入了22例MDA病例和20例对照病例,其中对照病例包括10例宫颈管小叶状腺体增生和10例正常宫颈组织。收集了所有可用的临床资料,并对这些病例进行了FOXP1、癌胚抗原(CEA)、人乳脂肪球抗原1(HMFG1)、雌激素受体和孕激素受体的免疫染色。22例MDA病例中有18例出现FOXP1核/胞质表达,而20例对照病例中仅有1例出现,差异具有统计学意义(P = .000)。22例MDA病例中有14例出现胞质CEA表达,20例对照病例中有2例出现(P = .000),而22例MDA病例中有10例出现胞质HMFG1表达,20例对照病例中有4例出现(P = .081)。MDA中FOXP1与CEA表达之间(P = .083)或FOXP1与HMFG1表达之间(P = .375)无统计学差异。MDA中未发现雌激素受体和孕激素受体表达。FOXP1在MDA中的显著表达在一定程度上可能有助于宫颈MDA的病理诊断。需要扩大观察范围并进一步研究以阐明其潜在机制。