Nkosi Dingani, Crowe William E, Altman Brian J, Oltvai Zoltán N, Giampoli Ellen J, Velez Moises J
Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY, 14642, USA.
Department of Biomedical Genetics, University of Rochester School of Medicine and Dentistry, Rochester, NY, 14642, USA.
Endocr Pathol. 2024 Dec;35(4):432-441. doi: 10.1007/s12022-024-09833-0. Epub 2024 Nov 5.
Anaplastic thyroid carcinoma (ATC) is a rare and aggressive thyroid malignancy typically comprised of undifferentiated tumor cells with various histologic morphologies, which makes the diagnosis challenging. These tumors commonly show loss of thyroglobulin and TTF1 with preservation of cytokeratin (67%) and Paired Box Gene 8 (PAX8) (55%) expression. Identification of a sensitive immunohistochemical stain to aid in the diagnosis of ATC would be beneficial. Immunohistochemistry (IHC) against special AT-rich sequence-binding protein 2 (SATB2) protein is a sensitive and specific marker expressed in colorectal adenocarcinoma and bone or soft tissue tumors with osteoblastic differentiation. However, SATB2 is also expressed in other sarcomatous/undifferentiated neoplasms lacking osteoblastic differentiation. Using quantitative reverse transcription PCR (RT-qPCR) we showed that there is variable expression of SATB2 mRNA expression in ATCs. To evaluate the role of SATB2 protein expression in ATC, we performed PAX8, SATB2, pancytokeratin (AE1/AE3 & CAM5.2), claudin-4 and TTF1 immunostaining on 23 cases. ATCs showed retained expression of PAX8 in 65% (15/23); SATB2 was detected in 74% (17/23); pancytokeratin was expressed in 65% (15/23); claudin-4 was expressed in 35% (8/23) and TTF1 showed expression in 13% (3/23) of cases. Furthermore, 83% (5/6) of ATCs which lacked SATB2 expression, retained PAX8 expression, while 88% (7/8) of the tumors without PAX8 expression were positive for SATB2. Differentiated follicular cell-derived thyroid cancers (n = 30), differentiated high grade thyroid carcinoma (n = 3), and poorly differentiated thyroid carcinoma (n = 8) were negative for SATB2 immunoreactivity. Next-generation selected cases detected the commonly identified oncogenic variants including those in BRAF, RAS, TP53, and TERT promoter. Overall, we hereby demonstrate that SATB2 IHC may be used to support the diagnosis of ATC.
间变性甲状腺癌(ATC)是一种罕见且侵袭性强的甲状腺恶性肿瘤,通常由具有各种组织学形态的未分化肿瘤细胞组成,这使得诊断具有挑战性。这些肿瘤通常显示甲状腺球蛋白和TTF1缺失,而细胞角蛋白(67%)和配对盒基因8(PAX8)(55%)表达保留。鉴定一种有助于ATC诊断的敏感免疫组化染色将是有益的。针对富含AT序列的特殊结合蛋白2(SATB2)蛋白的免疫组化(IHC)是一种在结直肠癌以及具有成骨细胞分化的骨或软组织肿瘤中表达的敏感且特异的标志物。然而,SATB2在其他缺乏成骨细胞分化的肉瘤样/未分化肿瘤中也有表达。我们通过定量逆转录PCR(RT-qPCR)显示,SATB2 mRNA在ATC中的表达存在差异。为了评估SATB2蛋白表达在ATC中的作用,我们对23例病例进行了PAX8、SATB2、全细胞角蛋白(AE1/AE3和CAM5.2)、claudin-4和TTF1免疫染色。ATC中65%(15/23)显示PAX8表达保留;74%(17/23)检测到SATB2;65%(15/23)表达全细胞角蛋白;35%(8/23)表达claudin-4,13%(3/23)的病例显示TTF1表达。此外,83%(5/6)缺乏SATB2表达的ATC保留了PAX8表达,而88%(7/8)无PAX8表达的肿瘤SATB2呈阳性。分化型滤泡细胞来源的甲状腺癌(n = 30)、分化型高级别甲状腺癌(n = 3)和低分化甲状腺癌(n = 8)SATB2免疫反应性均为阴性。下一代选定病例检测到常见的致癌变异,包括BRAF、RAS、TP53和TERT启动子中的变异。总体而言,我们在此证明SATB2免疫组化可用于支持ATC的诊断。