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葡萄膜黑色素瘤的基因图谱

Genetic landscape of uveal melanoma.

作者信息

Rodrigues M J, Stern M-H

机构信息

Institut Curie, centre de recherche, Inserm U830, 26, rue d'Ulm, 75248 Paris cedex 05, France.

Institut Curie, centre de recherche, Inserm U830, 26, rue d'Ulm, 75248 Paris cedex 05, France.

出版信息

J Fr Ophtalmol. 2015 Jun;38(6):522-5. doi: 10.1016/j.jfo.2015.04.004. Epub 2015 May 11.

Abstract

Uveal melanoma is genetically one of the simplest malignant tumors in adults. Initiation of these tumors is dependent of an oncogenic mutation in the GNAQ or GNA11 genes present in almost all cases. The nature of second mutational events is of major interest as it monosomy 3, gain of 8q and BAP1 inactivation are associated with unfavorable prognosis while SF3BI or EIF1AX are of good prognosis. Despite their common lineage, cutaneous and uveal melanomas are distinct diseases, implicating different oncogenic pathways and contrasting mutational landscapes. Even if uveal melanoma is a simple tumor, it is also one of the deadliest tumors in adults. There is a major clinical need for drugs targeting either the downstream pathways of Gαq and Gα11 or the biological cell functions dysregulated by BAP1 loss of function.

摘要

葡萄膜黑色素瘤在基因层面是成人中最简单的恶性肿瘤之一。这些肿瘤的发生几乎在所有病例中都依赖于GNAQ或GNA11基因中的致癌突变。第二个突变事件的性质备受关注,因为3号染色体单体、8号染色体长臂增加和BAP1失活与不良预后相关,而SF3BI或EIF1AX则与良好预后相关。尽管皮肤黑色素瘤和葡萄膜黑色素瘤有着共同的起源,但它们是不同的疾病,涉及不同的致癌途径和截然不同的突变格局。即使葡萄膜黑色素瘤是一种简单的肿瘤,它也是成人中最致命的肿瘤之一。临床上迫切需要针对Gαq和Gα11下游途径或因BAP1功能丧失而失调的生物细胞功能的药物。

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