Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
UT Southwestern Medical Center, Clements University Hospital UH04.234, 6201 Harry Hines Boulevard, Dallas, TX, 75390, USA.
Head Neck Pathol. 2022 Dec;16(4):1146-1156. doi: 10.1007/s12105-022-01476-z. Epub 2022 Aug 6.
GLI1 is a transcription factor protein that has recently gained recognition in a morphologically distinct group of epithelioid soft tissue tumors characterized by GLI1 fusions or amplifications. The head and neck region, particularly the tongue, is a common location for GLI1-altered tumors. DDIT3 break apart fluorescence in situ hybridization (FISH), commonly used to identify translocations in myxoid/round cell liposarcoma, has been used as a surrogate test to detect both fusions and amplifications of the 12q13.3 region encompassing DDIT3 and GLI1 gene loci.
We herein report 5 cases of GLI1-altered soft tissue tumors. Three arose in the oropharynx (base of tongue/vallecula, tonsil) and two arose in the tongue. Given the frequent oropharyngeal location and epithelioid morphology, p16 immunohistochemistry was performed on cases with available material. Commercially available DDIT3 break apart FISH, custom GLI1 specific FISH, and RNA sequencing were performed on select cases.
Two cases showed amplification using DDIT3 FISH which was confirmed using GLI1 specific FISH. The remaining cases harbored ACTB::GLI1, one of which showed rearrangement of the 12q13.3 region by DDIT3 FISH with absence of amplification by GLI1 specific FISH. STAT6 immunoexpression was positive in the GLI1-amplified cases and negative in the GLI1-rearranged cases while MDM2 expression was positive in the 4 cases tested. CDK4 expression was strong and diffuse in the GLI1-amplified cases. p16 immunohistochemistry showed strong nuclear and cytoplasmic staining in 50-70% of tumor cells in all four tested cases.
Here we show that GLI1-altered soft tissue tumors are frequently positive for p16 and can occur in tonsillar regions of the oropharynx. As such, positive p16 immunohistochemistry alone cannot be used as evidence for the diagnosis of HPV-related squamous cell carcinoma as strong and diffuse p16 expression may also occur in GLI1-altered soft tissue tumors. Commercially available DDIT3 break apart FISH, which is readily available in many cytogenetic laboratories, may be useful as a sensitive surrogate test for GLI1 fusions and amplifications.
GLI1 是一种转录因子蛋白,最近在一组形态学上不同的上皮样软组织肿瘤中得到了认识,这些肿瘤的特征是 GLI1 融合或扩增。头颈部,特别是舌部,是 GLI1 改变的肿瘤的常见部位。DDIT3 分离荧光原位杂交(FISH),通常用于识别黏液/圆形细胞脂肪肉瘤中的易位,已被用作检测包括 DDIT3 和 GLI1 基因座在内的 12q13.3 区域融合和扩增的替代试验。
我们在此报告 5 例 GLI1 改变的软组织肿瘤。其中 3 例发生在口咽(舌根/ vallecula、扁桃体),2 例发生在舌部。鉴于常见的口咽位置和上皮样形态,对有可用材料的病例进行了 p16 免疫组化染色。对选定的病例进行了商业上可用的 DDIT3 分离 FISH、定制的 GLI1 特异性 FISH 和 RNA 测序。
2 例病例显示 DDIT3 FISH 扩增,并用 GLI1 特异性 FISH 证实。其余病例均存在 ACTB::GLI1,其中 1 例通过 DDIT3 FISH 显示 12q13.3 区域重排,而 GLI1 特异性 FISH 未见扩增。在 GLI1 扩增的病例中 STAT6 免疫表达阳性,在 GLI1 重排的病例中为阴性,而在 4 例测试的病例中 MDM2 表达阳性。CDK4 在 GLI1 扩增的病例中呈强而弥漫的表达。在所有 4 例测试的病例中,p16 免疫组化显示肿瘤细胞的 50-70%呈强核和胞质染色。
我们的研究表明,GLI1 改变的软组织肿瘤通常为 p16 阳性,并且可能发生在口咽的扁桃体区域。因此,仅凭阳性的 p16 免疫组化不能作为 HPV 相关鳞状细胞癌的诊断证据,因为在 GLI1 改变的软组织肿瘤中也可能出现强而弥漫的 p16 表达。商业上可用的 DDIT3 分离 FISH,在许多细胞遗传学实验室都很容易获得,可能是检测 GLI1 融合和扩增的一种敏感替代试验。