免疫组织化学检测 YAP1 N 端和 C 端可通过不同的染色模式突出显示变性胸腺瘤和高级别胸腺上皮肿瘤

IF 3.4 3区 医学 Q1 PATHOLOGY
Yosuke Yamada, Stefan Küffer, Christian Sauer, Masahito Hoki, Shinsuke Shibuya, Hideaki Tsujii, Kazuo Ono, Koki Moriyoshi, Hiroshi Date, Akihiko Yoshizawa, Malgorzata Szolkowska, Hironori Haga, Phillip Ströbel, Alexander Marx
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引用次数: 0

摘要

变性胸腺瘤(MT)是胸腺上皮性肿瘤(TET)的一种罕见亚型,它携带YAP1::MAML2融合。皮肤肿瘤 Poroma 也携带这些融合,并表现出独特的 YAP1 免疫组织化学(IHC)染色模式,即 YAP1 N 端(YAP1[N])阳性但 YAP1 C 端(YAP1[C])阴性的模式。在这种情况下,最近有报告称,在 TET 亚型中,MT 独家缺乏 YAP1(C) 表达。然而,由于该研究中缺乏有关 YAP1(N) 表达的信息,且另有报道称野生型 YAP1 在 B3 型胸腺瘤和胸腺癌中的表达减少,因此有必要进一步研究 YAP1 在 TET 中的表达。因此,我们用免疫组化方法检测了包括14例MT在内的TET样本中YAP1(N)和YAP1(C)的染色模式。此外,我们还对 14 例 MT 中的 11 例进行了福尔马林固定石蜡包埋组织的基因分析,以确定它们是否携带 YAP1::MAML2 融合。MT始终表现为YAP1(N)阳性和YAP(C)阴性染色,而B3型胸腺瘤和胸腺癌则表现出相对不均匀的YAP1(N)和YAP1(C)染色模式,有时两种抗体均为阴性。此外,与B2型胸腺瘤相比,B3型胸腺瘤的YAP1表达量较低。在经过基因分析的11例MT病例中,有6例出现了YAP1::MAML2融合,而5例年龄较大的病例由于RNA质量较差,分析失败。这些结果表明,建议同时对YAP1(N)和YAP1(C)进行IHC检测,以获得几乎是MT特有的染色模式。YAP1在高级别TET中的生物学意义值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immunohistochemistry for YAP1 N-terminus and C-terminus highlights metaplastic thymoma and high-grade thymic epithelial tumors by different staining patterns

Immunohistochemistry for YAP1 N-terminus and C-terminus highlights metaplastic thymoma and high-grade thymic epithelial tumors by different staining patterns

Metaplastic thymoma (MT), a rare subtype of thymic epithelial tumors (TETs), harbors YAP1::MAML2 fusions. Poroma, a skin tumor, also carries these fusions and exhibits a unique staining pattern for YAP1 immunohistochemistry (IHC), namely, a YAP1 N-terminus (YAP1[N])-positive but YAP1 C-terminus (YAP1[C])-negative pattern. In this context, MT was recently reported to lack YAP1(C) expression exclusively among TET subtypes. However, a lack of information about YAP1(N) expression in that study and another report that wild-type YAP1 expression was diminished in type B3 thymoma and thymic carcinoma warrants further studies for YAP1 expression in TETs. Thus, we immunohistochemically examined YAP1(N) and YAP1(C) staining patterns in our TET samples, including 14 cases of MT. In addition, 11 of the 14 MT cases were genetically analyzed with the formalin-fixed paraffin-embedded tissues if they harbored YAP1::MAML2 fusions. MT consistently exhibited YAP1(N)-positive and YAP(C)-negative staining, whereas type B3 thymoma and thymic carcinoma showed relatively heterogeneous staining patterns for YAP1(N) and YAP1(C) and were sometimes negative for both antibodies. Furthermore, a lower expression of YAP1 was found in type B3 compared to B2 thymomas. Among genetically analyzed 11 MT cases, 6 cases showed YAP1::MAML2 fusions, whereas the analysis failed in 5 very old cases due to poor RNA quality. These results indicate that IHC of both YAP1(N) and YAP1(C) is recommended to obtain staining patterns almost unique to MT. The biological significance of YAP1 in high-grade TETs warrants further investigation.

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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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