NKX3-1是EWSR1-NFATC2肉瘤和间充质软骨肉瘤的有效免疫组织化学标志物

Ken-Ichi Yoshida, Isidro Machado, Toru Motoi, Antonina Parafioriti, Maribel Lacambra, Hitoshi Ichikawa, Akira Kawai, Cristina R Antonescu, Akihiko Yoshida
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引用次数: 41

摘要

NK3同源盒1 (NKX3-1)被广泛认为是前列腺癌高度敏感和特异性的标志物。根据已发表的转录组数据显示,NKX3-1 mRNA在EWSR1-NFATC2肉瘤中的表达上调,我们探索了NKX3-1免疫组织化学在肉瘤诊断中的应用。我们对11例EWSR1-NFATC2肉瘤和168例全组织切片模拟瘤应用NKX3-1免疫组化。所有EWSR1-NFATC2肉瘤均由均匀的小圆形或卵形细胞组成,除1例外,其余肉瘤均在纤维/黏液样背景下至少局部表现出巢状、索状或小梁的典型生长模式。易变的嗜酸性粒细胞浸润是常见的。11例EWSR1-NFATC2肉瘤中有9例(82%)表达NKX3-1,常为弥漫性、中等或强强度。所有12个间充质软骨肉瘤检测均为NKX3-1阳性,半数以上为弥漫性染色,强度中等或较强。仅原始小圆细胞成分呈阳性,软骨成分多呈阴性。虽然30例骨肉瘤中有1例局灶性NKX3-1阳性,但其余155例,包括20例尤文氏肉瘤、20例肌上皮肿瘤、11例骨化纤维黏液样肿瘤和1例FUS-NFATC2肉瘤,均为NKX3-1阴性。我们的研究首次提供了EWSR1-NFATC2肉瘤和Ewing肉瘤可以通过免疫组织化学方法区分的证据,增加了这些肿瘤在表型上不同的积累数据。我们认为NKX3-1可能在肉瘤的诊断中具有实用价值,同时我们也提醒人们注意使用这种众所周知的前列腺腺癌标记物的潜在缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NKX3-1 Is a Useful Immunohistochemical Marker of EWSR1-NFATC2 Sarcoma and Mesenchymal Chondrosarcoma.

NK3 homeobox 1 (NKX3-1) is widely accepted as a highly sensitive and specific marker for prostatic adenocarcinoma. Prompted by published transcriptome data showing upregulation of NKX3-1 mRNA expression in EWSR1-NFATC2 sarcoma, we explored the utility of NKX3-1 immunohistochemistry in sarcoma diagnosis. We applied NKX3-1 immunohistochemistry to 11 EWSR1-NFATC2 sarcomas and 168 mimics using whole tissue sections. All EWSR1-NFATC2 sarcomas consisted of uniform small round or ovoid cells, all except 1 showing at least focally the typical growth pattern of nests, cords, or trabeculae within a fibrous/myxoid background. A variable eosinophilic infiltrate was common. NKX3-1 was expressed in 9 of 11 (82%) EWSR1-NFATC2 sarcomas, often diffuse and of moderate or strong intensity. All 12 mesenchymal chondrosarcomas tested were also positive for NKX3-1, with over half showing diffuse staining and moderate or strong intensity. The positive staining was seen only in the primitive small round cell component, whereas the cartilaginous component was mostly negative. Although 1 of 30 osteosarcomas showed focal NKX3-1 positivity, all the remaining 155 cases tested, including 20 Ewing sarcomas, 20 myoepithelial tumors, 11 ossifying fibromyxoid tumors, and 1 FUS-NFATC2 sarcoma were negative for NKX3-1. Our study provides the first evidence that EWSR1-NFATC2 sarcoma and Ewing sarcoma could be distinguished immunohistochemically, adding to the accumulating data that these tumors are phenotypically distinct. We suggest that NKX3-1 may have a diagnostic utility in the evaluation of sarcoma and we also call attention to potential pitfalls in the use of this well-known marker of prostatic adenocarcinoma.

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