Utilization of NKX3.1 and P501S to distinguish primary breast carcinoma from metastatic prostatic adenocarcinoma in male patients.

IF 3.4 3区 医学 Q1 PATHOLOGY
Mustafa Goksel, Chirag R Patel, Sarah A Anderson, Gian Piero Carames, Sandra S Moultrie, Cristina Magi-Galluzzi, Shi Wei, Xiao Huang
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Abstract

NKX3.1 is an androgen-regulated tumor suppressor gene, and NKX3.1 protein expression is present mainly in prostatic epithelium. P501S is expressed in prostatic epithelium and is also regulated by androgens. Immunohistochemistry (IHC) for NKX3.1 and P501S is commonly used for the diagnosis of metastatic prostate carcinoma in pathology practice. Male breast cancer is rare, and most of the tumors are androgen-receptor positive. Thus, we investigated NKX3.1 and P501S expression in male breast carcinoma to determine its role in distinguishing primary breast carcinoma from metastatic prostatic adenocarcinoma. IHC for NKX3.1 and P501S was performed on primary invasive breast carcinomas in 25 male patients, 5 of whom had prior history of prostatic adenocarcinoma. Immunoreactivity was classified as negative or positive staining. Expression of NKX3.1 and P501S was identified in 8 (32%) and 7 (28%) cases of invasive breast carcinomas, 42% and 20% of in situ breast carcinomas, and 8% and 46% of normal terminal ductal lobular unit (TDLU), respectively. Among the five patients with prior history of prostate carcinoma, four had NKX3.1 or P501S expression in their primary invasive breast carcinomas. Their diagnosis of primary invasive breast carcinomas was confirmed by GATA3 and estrogen receptor (ER) IHC. This is the first study to report NKX3.1 and P501S expression in primary breast carcinomas in male patients. The positive rates are higher than those reported in female patients with ductal carcinoma. When considering the use of IHC markers to confirm the diagnosis of primary breast carcinoma in male patients, breast-specific markers or hormonal receptors should be considered in the diagnostic panel.

应用NKX3.1和P501S鉴别男性原发性乳腺癌和转移性前列腺腺癌。
NKX3.1是一种雄激素调控的肿瘤抑制基因,NKX3.1蛋白主要表达于前列腺上皮。P501S在前列腺上皮中表达,也受雄激素调节。在病理实践中,NKX3.1和P501S的免疫组化(IHC)是诊断转移性前列腺癌的常用方法。男性乳腺癌是罕见的,大多数肿瘤是雄激素受体阳性。因此,我们研究了NKX3.1和P501S在男性乳腺癌中的表达,以确定其在区分原发性乳腺癌和转移性前列腺腺癌中的作用。对25例男性原发性浸润性乳腺癌患者进行NKX3.1和P501S免疫组化检测,其中5例既往有前列腺腺癌病史。免疫反应性分为阴性或阳性染色。NKX3.1和P501S在浸润性乳腺癌中分别表达8例(32%)和7例(28%),原位乳腺癌中分别表达42%和20%,正常末端导管小叶单位(TDLU)中分别表达8%和46%。5例既往有前列腺癌病史的患者中,4例原发浸润性乳腺癌中有NKX3.1或P501S表达。经GATA3和雌激素受体(ER)免疫组化检测证实为原发性浸润性乳腺癌。本研究首次报道了NKX3.1和P501S在男性原发性乳腺癌患者中的表达。阳性检出率高于女性导管癌。在考虑使用免疫组化标志物确认男性患者原发性乳腺癌诊断时,应在诊断组中考虑乳腺特异性标志物或激素受体。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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