肾上皮样血管瘤在没有TFE3重排的情况下过度表达TFE3和TFE3调控基因TRIM63。

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-07-07 DOI:10.1007/s00428-024-03855-z
Katrina Collins, Julia A Bridge, Rohit Mehra, Rahul Mannan, Brendan C Dickson, Tamara L Lotan, Muhammad T Idrees, Thomas M Ulbright, Andres M Acosta
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引用次数: 0

摘要

血管脂肪瘤(AML)是血管周围上皮细胞瘤家族中的一种肿瘤,常发生于肾脏。大多数肿瘤症状不明显,是偶然发现的,只有极少数肿瘤具有恶性临床表现。一小部分具有上皮样特征的肾脏急性髓细胞瘤具有侵袭性,并可能与肾细胞癌(如透明细胞肾细胞癌(RCC)、TFE3重排RCC)在形态学上重叠。先前对纺锤形细胞和上皮样急性髓细胞癌的研究发现了一些罕见的具有潜在 TFE3 基因融合的病例。之前有报道称,在 4/24 例急性髓细胞性白血病(17%)中存在 TFE3 蛋白表达(免疫组化证明),但无证据表明同时存在 TFE3 基因重排(Argani 等,Am J Surg Pathol 34:1395-1406,2010 年)。目前,人们对肾上皮样急性髓细胞性白血病中 TFE3 蛋白表达、TFE3 融合和 TFE3 介导的基因表达之间的关系仍不完全清楚。我们试图利用TFE3断裂荧光原位杂交(FISH)和TRIM63 RNA原位杂交(ISH)对免疫组化法检测TFE3中度至高度表达的上皮样AMLs探索这些关系。对两例FISH结果为阴性的病例进行了RNA测序(融合面板),以评估FISH-密码基因融合。该系列包括来自四名患者(三名女性,一名男性)的五例上皮样急性髓细胞白血病,患者年龄在13至76岁之间。通过免疫组化(2 + /3 + 表达),所有患者的 TFE3 均为阳性。对 3 名患者的 4 份标本进行了 TRIM63 ISH 分析,结果显示 3/3 的肿瘤呈阳性(100%),分析成功。对所有样本进行了TFE3断裂FISH检测,只有1/4的肿瘤(25%)出现了TFE3重排。RNA 测序表明,在 TFE3 分位 FISH 结果为阴性的三个肿瘤中,不存在生产性 TFE3 基因融合。这项研究表明,即使没有TFE3基因重排,肾上皮样AML也会过表达TFE3和TFE3介导的基因(TRIM63)。这一发现可能是由于雷帕霉素哺乳动物靶标复合体 1(mTORC1)的激活导致了 TFE3 的功能性上调。鉴于上皮样急性髓细胞癌和TFE3改变的肾细胞癌在形态学和免疫表型上的重叠,TFE3和TRIM63在这种肿瘤类型中的表达是一个潜在的陷阱。
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Renal epithelioid angiomyolipomas overexpress TFE3 and the TFE3-regulated gene TRIM63 in the absence of TFE3 rearrangement.

Angiomyolipoma (AML) is a neoplasm within the perivascular epithelioid cell tumor family that occurs somewhat frequently in the kidney. Most are indolent and discovered incidentally, with rare tumors demonstrating malignant clinical behavior. A small subset of renal AMLs with epithelioid features are associated with aggressive behavior, and may demonstrate morphologic overlap with renal cell carcinomas (e.g., clear cell renal cell carcinoma (RCC), TFE3-rearranged RCC). Prior studies of spindle cell and epithelioid AMLs have identified rare examples with underlying TFE3 gene fusions. TFE3 protein expression (demonstrated by immunohistochemistry) with no evidence of concurrent TFE3 rearrangements has been reported previously in 4/24 AMLs (17%) (Argani et al. Am J Surg Pathol 34:1395-1406, 2010). Currently, the relationship between TFE3 protein expression, TFE3 fusions, and expression of TFE3-mediated genes remains incompletely understood in renal epithelioid AMLs. We sought to explore these relationships using TFE3 break-apart fluorescence in situ hybridization (FISH) and TRIM63 RNA in situ hybridization (ISH) on epithelioid AMLs with moderate to strong TFE3 expression by immunohistochemistry. RNA sequencing (fusion panel) was performed on two cases with negative FISH results to assess for FISH-cryptic gene fusions. The series comprised five epithelioid AMLs from four patients (three women, one man) aged 13 to 76 years. All were considered positive for TFE3 by immunohistochemistry (2 + /3 + expression). TRIM63 ISH was performed on four specimens from three patients, yielding positive results in 3/3 tumors (100%) that were successfully analyzed. TFE3 break-apart FISH was performed on all samples, demonstrating a TFE3 rearrangement in only 1/4 tumors (25%). RNA sequencing demonstrated the absence of productive TFE3 gene fusions in three tumors with negative break-apart TFE3 FISH results. This study demonstrates that renal epithelioid AMLs overexpress TFE3 and TFE3-mediated genes (TRIM63) even in the absence of TFE3 rearrangements. This finding could be explained by functional upregulation of TFE3 secondary to activation of the mammalian target of rapamycin complex 1 (mTORC1). Expression of TFE3 and TRIM63 in this tumor type represents a potential pitfall, given the morphologic and immunophenotypic overlap between epithelioid AML and TFE3-altered renal cell carcinoma.

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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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