CD56 (Neural Cell Adhesion Molecule) Expression in Ovarian Carcinomas: Association With High-Grade and Advanced Stage But Not With Neuroendocrine Differentiation.

Hans-Christian Bösmüller, Philipp Wagner, Deborah Lam Pham, Anna K Fischer, Karen Greif, Christine Beschorner, Bence Sipos, Falko Fend, Annette Staebler
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Abstract

Objective: Neural cell adhesion molecule (CD56) has been proposed as a potential marker for neuroendocrine differentiation in carcinomas, together with synaptophysin and chromogranin A. However, CD56 immunoreactivity by itself can be found in a broad variety of tumors, including ovarian neoplasms. CD56 has recently been suggested as a potential target for antibody-based therapy. However, for ovarian carcinoma, there is only limited data available regarding the pattern of CD56 immunoreactivity, coexpression of neuroendocrine markers, and correlation with histological types and clinical parameters.

Methods: In our study, we therefore evaluated CD56 staining by immunohistochemistry on a tissue micrroarray with 206 ovarian carcinomas, including 151 high-grade serous, 7 low-grade serous, 32 endometrioid, 11 clear cell, 5 mucinous, as well as 33 atypically proliferating serous tumors/serous borderline tumors.

Results: At least focal CD56 immunoreactivity was observed in 65% of carcinomas of all histological types. Moderate staining with at least 10% positive cells was found in 44 (28%) high-grade serous carcinomas (HGSOCs), 2 (29%) low-grade serous and 3(9%) endometrioid carcinomas. Strong immunoreactivity was limited to 10 (7%) HGSOCs. There was no correlation with the expression of chromogranin or synaptophysin. Serous borderline tumors showed only weak and focal staining in 11 (33%). Expression of CD56 overall was significantly associated with high-grade and advanced stage. In the subgroup of HGSOCs, CD56 expression was associated with reduced overall survival (median 30 vs. 47 months, P = 0.039, log rank, univariate analysis).

Conclusions: CD56 (neural cell adhesion molecule) is frequently expressed in ovarian carcinomas and is significantly associated with HGSOC and advanced tumor stage. Due to its lack of correlation with neuroendocrine differentiation, CD56 expression is of limited diagnostic value, but may rather serve as a marker for tumor progression or as a potential therapeutic target.

CD56(神经细胞粘附分子)在卵巢癌中的表达:与高级别和晚期肿瘤有关,但与神经内分泌分化无关。
目的:神经细胞粘附分子(Neural cell adhesion molecule, CD56)与synaptophysin和chromogranin a一起被认为是肿瘤神经内分泌分化的潜在标志物。然而,CD56本身的免疫反应性可以在包括卵巢肿瘤在内的多种肿瘤中发现。CD56最近被认为是基于抗体治疗的潜在靶点。然而,对于卵巢癌,关于CD56免疫反应模式、神经内分泌标志物的共表达以及与组织学类型和临床参数的相关性的数据有限。方法:在我们的研究中,我们用免疫组织化学方法对206例卵巢癌的组织微阵列进行了CD56染色评估,其中包括151例高级别浆液性、7例低级别浆液性、32例子宫内膜样、11例透明细胞、5例粘液性和33例非典型增殖浆液性肿瘤/浆液性交界性肿瘤。结果:在所有组织学类型中,65%的癌至少有局灶性CD56免疫反应性。在44例(28%)高级别浆液性癌(HGSOCs)、2例(29%)低级别浆液性癌和3例(9%)子宫内膜样癌中发现至少10%阳性细胞的中度染色。强免疫反应性仅限于10个(7%)hgsoc。与嗜铬粒蛋白、突触素的表达无相关性。浆液性交界性肿瘤仅11例(33%)呈弱灶性染色。CD56的表达总体上与高级别和晚期有显著相关性。在hgsoc亚组中,CD56表达与总生存期降低相关(中位30个月vs. 47个月,P = 0.039, log rank,单变量分析)。结论:CD56(神经细胞粘附分子)在卵巢癌中频繁表达,并与HGSOC和肿瘤分期显著相关。由于其与神经内分泌分化缺乏相关性,CD56表达的诊断价值有限,但可以作为肿瘤进展的标志或作为潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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