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表达 CTAG1B 克隆 EPR13780 与基因重排可区分黏液样脂肪肉瘤与其模拟物,并检测到新的基因拷贝数变异。

Expression of CTAG1B clone EPR13780 versus gene rearrangement distinguishes myxoid liposarcoma from its mimics with detection of novel gene copy number variations.

机构信息

Department of Pathology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.

Department of Pathology, National Cancer Institute, Cairo University, Cairo, Egypt.

出版信息

J Histotechnol. 2022 Jun;45(2):56-65. doi: 10.1080/01478885.2021.2004294. Epub 2021 Nov 30.

Abstract

Myxoid liposarcoma (MLPS) has different patterns that are often difficult to distinguish from other soft tissue lesions. MLPS is characterized by a reciprocal translocation involving the DNA Damage Inducible Transcript 3 gene that can be detected using fluorescent in situ hybridization (FISH). Recently, the marker for cancer testis antigen 1b (CTAG1B) was found to be expressed in MLPS. The aim of the present study was to assess the potential use immunohistochemistry (IHC) for CTAG1B expression and rearrangement to diagnose MLPS and distinguish it from similar lesions. Out of 29 cases including MLPS and its mimics, CTAG1B was expressed in 92.86% of cases of MLPS and 20% of its mimics. rearrangement was 100% sensitive and 92.86% specific in distinguishing MLPS from its mimics. The rearrangement was found to be more sensitive but less specific than cytoplasmic expression of CTAG1B marker. polysomy and amplification were detected in some cases. Therefore, both CTAG1B expression and FISH for gene can be used to distinguish MLPS from similar tumors. The use of both immunohistochemistry for CTAG1B in addition to gene rearrangement detection by FISH was more specific than using either of them alone. However, the gene rearrangement alone was the most sensitive test for distinguishing MLPS from its mimics.

摘要

黏液样脂肪肉瘤(MLPS)具有不同的形态,常难以与其他软组织病变区分。MLPS 的特征是涉及 DNA 损伤诱导转录物 3 基因的相互易位,可通过荧光原位杂交(FISH)检测到。最近,发现癌症睾丸抗原 1b(CTAG1B)标志物在 MLPS 中表达。本研究旨在评估 CTAG1B 表达和 重排在诊断 MLPS 并将其与类似病变区分开来的潜在用途。在包括 MLPS 及其模拟物在内的 29 例中,CTAG1B 在 92.86%的 MLPS 病例和 20%的模拟物中表达。 重排在将 MLPS 与其模拟物区分开来方面的敏感性为 100%,特异性为 92.86%。发现 重排在区分 MLPS 与其模拟物方面比 CTAG1B 标志物的细胞质表达更敏感但特异性更低。在一些病例中检测到了 多倍体和扩增。因此,CTAG1B 表达和 基因的 FISH 均可用于区分 MLPS 与其类似肿瘤。与单独使用其中任何一种相比,同时使用 CTAG1B 的免疫组化和 FISH 检测 基因重排更具特异性。然而,仅使用 基因重排是区分 MLPS 与其模拟物的最敏感试验。

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