Pathogenic NF1 truncating mutation and copy number alterations in a dedifferentiated liposarcoma with multiple lung metastasis: a case report.

4区 医学 Q4 Medicine
Yoon-Seob Kim, Sun Shin, Seung-Hyun Jung, Yeun-Jun Chung
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引用次数: 1

Abstract

Background: Dedifferentiated liposarcoma (DDLPS), which accounts for an estimated 15-20% of liposarcomas, is a high-grade and aggressive malignant neoplasm, exhibiting a poor response to available therapeutic agents. However, genetic alteration profiles of DDLPS as well as the role of NF1 mutations have not been studied extensively.

Case presentation: The current study reports a patient presenting with rapidly growing DDLPS accompanied by multiple lung and pleural metastases, in whom whole-exome sequencing revealed a NF1 truncating mutation of the known pathogenic variant, c.C7486T, p.R2496X, as well as multiple copy number alterations (CNAs), including the well-known 12q13-15 amplification, and multiple chromothripsis events encompassing potential cancer-related genes.

Conclusions: Our results suggest that, in addition to the 12q13-15 amplification, NF1 inactivation mutation and other CNAs may contribute to DDLPS tumorigenesis accompanied by aggressive clinical features.

Abstract Image

Abstract Image

致病性NF1截断突变和拷贝数改变在多肺转移的去分化脂肪肉瘤:1例报告。
背景:去分化脂肪肉瘤(Dedifferentiated lipoarcoma, DDLPS)约占脂肪肉瘤的15-20%,是一种高度侵袭性恶性肿瘤,对现有治疗药物反应较差。然而,DDLPS的遗传改变谱以及NF1突变的作用尚未得到广泛研究。病例介绍:目前的研究报告了一名快速增长的DDLPS患者,并伴有多发性肺和胸膜转移,其中全外显子组测序显示已知致病变异c.C7486T, p.R2496X的NF1截断突变,以及多个拷贝数改变(CNAs),包括众所周知的12q13-15扩增,以及包含潜在癌症相关基因的多个染色体裂解事件。结论:我们的研究结果表明,除了12q13-15扩增外,NF1失活突变和其他CNAs可能有助于DDLPS的肿瘤发生,并伴有侵袭性临床特征。
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来源期刊
BMC Medical Genetics
BMC Medical Genetics 医学-遗传学
自引率
0.00%
发文量
0
审稿时长
12 months
期刊介绍: BMC Medical Genetics is an open access journal publishing original peer-reviewed research articles in the effects of genetic variation in individuals, families and among populations in relation to human health and disease. Note: BMC Medical Genetics is now closed. This journal has merged with BMC Medical Genomics, a broad-scope, open access community journal for all medical genetics and genomics research.
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