Goksel Mustafa, Patel Chirag R, Anderson Sarah A, Carames Gian Piero, Moultrie Sandra S, Magi-Galluzzi Cristina, Wei Shi, Huang Xiao
Department of Pathology, The University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL, 35294, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Phoenix, AZ, 85054, USA.
Virchows Arch. 2025 May 10. doi: 10.1007/s00428-025-04124-3.
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.
NKX3.1是一种雄激素调节的肿瘤抑制基因,NKX3.1蛋白表达主要存在于前列腺上皮中。P501S在前列腺上皮中表达,也受雄激素调节。在病理学实践中,NKX3.1和P501S的免疫组织化学(IHC)常用于转移性前列腺癌的诊断。男性乳腺癌罕见,且大多数肿瘤为雄激素受体阳性。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了NKX3.1和P501S的IHC检测,其中5例有前列腺腺癌病史。免疫反应性分为阴性或阳性染色。NKX3.1和P501S的表达分别在8例(32%)浸润性乳腺癌、42%的原位乳腺癌和8%的正常终末导管小叶单位(TDLU)中被检测到,在7例(28%)浸润性乳腺癌、20%的原位乳腺癌和46%的正常终末导管小叶单位中被检测到。在5例有前列腺癌病史的患者中,4例在其原发性浸润性乳腺癌中有NKX3.1或P501S表达。他们原发性浸润性乳腺癌的诊断通过GATA3和雌激素受体(ER)IHC得到证实。这是第一项报道男性原发性乳腺癌中NKX3.1和P501S表达的研究。阳性率高于导管癌女性患者的报道。在考虑使用IHC标志物来确诊男性原发性乳腺癌时,诊断组应考虑乳腺特异性标志物或激素受体。