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子宫复发性恶性苗勒管混合瘤中p16缺失

Loss of p16 in recurrent malignant mixed müllerian tumors of the uterus.

作者信息

Robinson-Bennett B, Belch R Z, Han A C

机构信息

Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The University of Texas Medical Branch, Galveston, TX, USA.

出版信息

Int J Gynecol Cancer. 2006 May-Jun;16(3):1354-7. doi: 10.1111/j.1525-1438.2006.00411.x.

Abstract

Uterine malignant mixed müllerian tumors (MMMTs) are rare and highly aggressive malignancies with poor clinical prognoses. We examined for differences in the oncoprotein profiles of primary versus recurrent MMMTs. Five cases of recurrent uterine MMMT were examined by paraffin immunohistochemistry for the expression of p53, p16, P-cadherin, and Cerb-B2. P16, p53, and P-cadherin were each expressed in 100%, 80%, and 60% of the primary cases, respectively. Three cases expressed all three oncoproteins. All five cases were negative for Cerb-B2. No difference in antigen expression was seen in the epithelial versus sarcomatous components. Primary and recurrent tumors were concordant for p53, P-cadherin, and Cerb-B2. However, three cases of recurrent tumors were negative for p16 expression. P53, p16, and P-cadherin are common tumor suppressor genes expressed in uterine MMMT. Interestingly, p16 protein expression was lost in some cases of MMMTs when they recurred. This suggests that the oncoprotein and possibly genetic profile of p16 changes over time. We did not observe any difference in antigen expression between areas of epithelial or sarcomatous differentiation, which would support a single pluripotential malignant clone in the histogenesis of these tumors.

摘要

子宫恶性苗勒管混合瘤(MMMTs)是罕见且具有高度侵袭性的恶性肿瘤,临床预后较差。我们研究了原发性与复发性MMMTs在癌蛋白谱方面的差异。通过石蜡免疫组织化学法检测了5例复发性子宫MMMT中p53、p16、P-钙黏蛋白和C-erbB-2的表达情况。在原发性病例中,p16、p53和P-钙黏蛋白的表达率分别为100%、80%和60%。3例同时表达了这三种癌蛋白。所有5例C-erbB-2均为阴性。上皮成分与肉瘤成分在抗原表达上未见差异。原发性和复发性肿瘤在p53、P-钙黏蛋白和C-erbB-2方面表现一致。然而,3例复发性肿瘤p16表达为阴性。p53、p16和P-钙黏蛋白是子宫MMMT中表达的常见肿瘤抑制基因。有趣的是,部分MMMTs复发时p16蛋白表达缺失。这表明p16的癌蛋白及可能的基因谱随时间发生了变化。我们未观察到上皮或肉瘤分化区域之间在抗原表达上有任何差异,这支持了这些肿瘤组织发生过程中存在单一多能性恶性克隆的观点。

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