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Detection and characterization of EWSR1|[sol]|ATF1 and EWSR1|[sol]|CREB1 chimeric transcripts in clear cell sarcoma (melanoma of soft parts)

机译:透明细胞肉瘤(软组织黑色素瘤)中EWSR1 | [sol] | ATF1和EWSR1 | [sol] | CREB1嵌合转录本的检测和鉴定

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Unlike melanoma, clear cell sarcoma harbors either a t(12;22)(q13;q12) recurrent translocation, resulting in an EWSR1/ATF1 chimeric gene, or less commonly a t(2;22)(q34;q12) translocation fusing EWSR1 and CREB1. Few studies have examined the prevalence of all chimeric types and variants to assess the usage of ancillary genetic testing in routine diagnosis. We investigated rearrangement prevalence in 17 clear cell sarcomas, two positive control cell lines, and two melanomas (negative controls). Fluorescence in situ hybridization (FISH) analysis using the LSI EWSR1 break-apart probe and a reverse transcription polymerase chain reaction (RT–PCR) assay optimized for formalin-fixed paraffin-embedded tissue to detect all four reported EWSR1/ATF1 clear cell sarcoma chimeric types and the EWSR1/CREB1 variant was performed. All 15 cases available for testing by FISH were positive for EWSR1 rearrangement including two cases with insufficient RNA for RT–PCR. Thirteen of 15 cases successfully tested by RT–PCR harbored a type 1 chimeric transcript (EWSR1 exon 8/ATF1 exon 4), of which five tumors simultaneously carried a type 2 chimeric transcript (EWSR1 exon 7/ATF1 exon 5). One case carried a type 2 transcript alone and one case contained an EWSR1/CREB1 transcript. Both control cases were positive by both techniques with one case carrying both types 1 and 2 chimeric transcripts and the other types 2 and 3 (EWSR1 exon 10/ATF1 exon 5). Consequently, both techniques are equally effective in assessing for an EWSR1 rearrangement and are useful ancillary diagnostic tests for clear cell sarcoma. They also reinforce the prevalence of this translocation in these tumors. In addition, EWSR1-CREB1 was identified in a clear cell sarcoma of soft tissue providing further evidence that this chimeric variant is not exclusive to gastrointestinal clear cell sarcomas and should be included in RT–PCR assays of soft tissue clear cell sarcomas.
机译:与黑素瘤不同,透明细胞肉瘤在(12; 22)(q13; q12)经常易位,导致产生EWSR1 / ATF1嵌合基因,而在(2; 22)(q34; q12)易位时融合了EWSR1和CREB1 。很少有研究检查所有嵌合类型和变异体的患病率,以评估辅助基因检测在常规诊断中的用途。我们调查了17个透明细胞肉瘤,两个阳性对照细胞系和两个黑色素瘤(阴性对照)中的重排患病率。荧光原位杂交(FISH)分析,使用LSI EWSR1分离探针和逆转录聚合酶链反应(RT-PCR)分析法,针对福尔马林固定石蜡包埋的组织进行了优化,可检测所有四个报道的EWSR1 / ATF1透明细胞肉瘤嵌合体类型和EWSR1 / CREB1变体。通过FISH检测的所有15例EWSR1重排均呈阳性,包括2例RNA不足以进行RT-PCR的病例。通过RT-PCR成功检测的15例病例中有13例具有1型嵌合转录本(EWSR1外显子8 / ATF1外显子4),其中五个肿瘤同时带有2型嵌合转录本(EWSR1外显子7 / ATF1外显子5)。 1例仅携带2型转录本,1例包含EWSR1 / CREB1转录本。通过两种技术,两个对照病例均为阳性,一个病例携带1型和2型嵌合转录本,另一个携带2型和3型(EWSR1外显子10 / ATF1外显子5)。因此,这两种技术在评估EWSR1重排方面均同样有效,并且对于透明细胞肉瘤也有用的辅助诊断测试。它们还增强了这些肿瘤中这种易位的发生率。此外,在软组织的透明细胞肉瘤中鉴定出EWSR1-CREB1,提供了进一步的证据,证明该嵌合变异体不是胃肠道透明细胞肉瘤所独有的,应包括在软组织透明细胞肉瘤的RT-PCR分析中。

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