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SYT-SSX基因融合作为滑膜肉瘤形态和预后的决定因素

SYT-SSX gene fusion as a determinant of morphology and prognosis in synovial sarcoma.

作者信息

Kawai A, Woodruff J, Healey J H, Brennan M F, Antonescu C R, Ladanyi M

机构信息

Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

N Engl J Med. 1998 Jan 15;338(3):153-60. doi: 10.1056/NEJM199801153380303.

Abstract

BACKGROUND

Synovial sarcomas account for up to 10 percent of soft-tissue sarcomas and include two major histologic subtypes, biphasic and monophasic, defined respectively by the presence and absence of glandular epithelial differentiation in a background of spindle tumor cells. A characteristic SYT-SSX fusion gene resulting from the chromosomal translocation t(X;18)(p11;q11) is detectable in almost all synovial sarcomas. The translocation fuses the SYT gene from chromosome 18 to either of two highly homologous genes at Xp11, SSX1 or SSX2. SYT-SSX1 and SYT-SSX2 are thought to tunction as aberrant transcriptional regulators. We attempted to determine the influence of the two alternative forms of the SYT-SSX fusion gene on tumor morphology and clinical outcome in patients with this sarcoma.

METHODS

We analyzed SYT-SSX fusion transcripts in 45 synovial sarcomas (33 monophasic and 12 biphasic) by the reverse-transcriptase polymerase chain reaction and compared the results with relevant clinical and pathological data.

RESULTS

The SYT-SSX1 and SYT-SSX2 fusion transcripts were detected in 29 (64 percent) and 16 (36 percent) of the tumors, respectively. There was a significant relation (P=0.003) between histologic subtype (monophasic vs. biphasic) and SSX1 or SSX2 involvement in the fusion transcript: all 12 biphasic synovial sarcomas had a SYT-SSX1 fusion transcript, and all 16 tumors that were positive for SYT-SSX2 were monophasic. Kaplan-Meier analysis of 39 patients with localized tumors showed that the 15 patients with SYT-SSX2 had significantly better metastasis-free survival than the 24 patients with SYT-SSX1 (P=0.03 by multivariate analysis; relative risk, 3.0). There were no significant correlations between the type of SYT-SSX transcript and age, sex, tumor location and size, whether there were metastases at diagnosis, or whether patients underwent chemotherapy. Histologic subtype alone was not prognostically important.

CONCLUSIONS

The type of SYT-SSX fusion transcript correlates with both the histologic subtype and the clinical behavior of synovial sarcoma. SYT-SSX fusion transcripts are a defining diagnostic marker of synovial sarcomas and may also yield important independent prognostic information.

摘要

背景

滑膜肉瘤占软组织肉瘤的比例高达10%,包括两种主要的组织学亚型,双相型和单相型,分别由梭形肿瘤细胞背景中是否存在腺上皮分化来定义。几乎在所有滑膜肉瘤中都可检测到由染色体易位t(X;18)(p11;q11)产生的特征性SYT-SSX融合基因。该易位将18号染色体上的SYT基因与Xp11上两个高度同源的基因之一,即SSX1或SSX2融合。SYT-SSX1和SYT-SSX2被认为作为异常转录调节因子发挥作用。我们试图确定SYT-SSX融合基因的两种替代形式对该肉瘤患者肿瘤形态和临床结局的影响。

方法

我们通过逆转录聚合酶链反应分析了45例滑膜肉瘤(33例单相型和12例双相型)中的SYT-SSX融合转录本,并将结果与相关临床和病理数据进行比较。

结果

在29例(64%)和16例(36%)肿瘤中分别检测到SYT-SSX1和SYT-SSX2融合转录本。组织学亚型(单相型与双相型)与融合转录本中SSX1或SSX2的参与情况之间存在显著相关性(P = 0.003):所有12例双相型滑膜肉瘤均有SYT-SSX1融合转录本,所有16例SYT-SSX2阳性肿瘤均为单相型。对39例局限性肿瘤患者进行的Kaplan-Meier分析显示,15例SYT-SSX2患者的无转移生存期明显优于24例SYT-SSX1患者(多因素分析P = 0.03;相对风险,3.0)。SYT-SSX转录本类型与年龄、性别、肿瘤位置和大小、诊断时是否有转移或患者是否接受化疗之间均无显著相关性。仅组织学亚型在预后方面并不重要。

结论

SYT-SSX融合转录本类型与滑膜肉瘤的组织学亚型和临床行为均相关。SYT-SSX融合转录本是滑膜肉瘤的决定性诊断标志物,也可能产生重要的独立预后信息。

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