由无性淋巴瘤激酶(ALK)基因融合引起的婴儿黑色素瘤。

IF 3.9 3区 医学 Q2 CELL BIOLOGY
Ifeoma U. Perkins, Serena Y. Tan, Timothy H. McCalmont, Pauline M. Chou, Thaddeus W. Mully, Pedram Gerami, Jason H. Pomerantz, Miguel Reyes-Múgica, Daniel M. Balkin, Lacey L. Kruse, Benjamin Huang, Jennifer L. Reichek, Noopur Gangopadhyay, Simon Chiosea, Jared R. Green, Sarah L. Chamlin, Ilona J. Frieden, Boris C. Bastian, Iwei Yeh
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引用次数: 0

摘要

我们描述了首例在巨大先天性黑素细胞痣中出现的ALK融合基因小儿黑色素瘤病例。两名新生男婴出现大面积色素结节性斑块和许多较小的卫星痣。两个痣内都出现了其他扩张性结节,两个男孩在10个月大前都被诊断出了浸润性黑色素瘤。两个病例中都没有 NRAS 和 BRAF 的致癌驱动基因突变。相反,在痣和痣内黑色素瘤中都发现了致癌的 ZEB2::ALK 融合基因。在这两个病例中,肿瘤都是在子宫内通过超声检查发现的,出生时表现为明显的结节,并在出生后第一年发展为黑色素瘤,这表明带有 ALK 融合基因的先天性痣可能比带有其他基因突变的痣更具侵袭性。由于ALK激酶抑制剂对一系列具有类似ALK融合激酶的肿瘤有效,因此在先天性黑素细胞痣中发现ALK融合基因可能为靶向治疗提供了机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Melanoma in infants, caused by a gene fusion involving the anaplastic lymphoma kinase (ALK)

We describe the first cases of pediatric melanoma with ALK fusion gene arising within giant congenital melanocytic nevi. Two newborn boys presented with large pigmented nodular plaques and numerous smaller satellite nevi. Additional expansile nodules developed within both nevi and invasive melanomas were diagnosed before 10 months of age in both boys. Oncogenic driver mutations in NRAS and BRAF were absent in both cases. Instead, oncogenic ZEB2::ALK fusion genes were identified in both the nevus and melanoma developing within the nevus. In both cases, tumors were noted by ultrasound in utero, demonstrated significant nodularity at birth, and progressed to melanoma in the first year of life suggesting that congenital nevi with ALK fusion genes may behave more aggressively than those with other mutations. As ALK kinase inhibitors are effective against a range of tumors with similar ALK fusion kinases, identifying ALK fusion genes in congenital melanocytic nevi may provide an opportunity for targeted therapy.

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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders
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