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葡萄膜黑素瘤中的剪接体突变。

Spliceosome Mutations in Uveal Melanoma.

机构信息

Department of Ophthalmology, Erasmus MC University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.

Department of Clinical Genetics, Erasmus MC University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.

出版信息

Int J Mol Sci. 2020 Dec 15;21(24):9546. doi: 10.3390/ijms21249546.

Abstract

Uveal melanoma (UM) is the most common primary intraocular malignancy of the eye. It has a high metastatic potential and mainly spreads to the liver. Genetics play a vital role in tumor classification and prognostication of UM metastatic disease. One of the driver genes mutated in metastasized UM is subunit 1 of splicing factor 3b (), a component of the spliceosome complex. Recurrent mutations in components of the spliceosome complex are observed in UM and other malignancies, suggesting an important role in tumorigenesis. is the most common mutated spliceosome gene and in UM it is associated with late-onset metastasis. This review summarizes the genetic and epigenetic insights of spliceosome mutations in UM. They form a distinct subgroup of UM and have similarities with other spliceosome mutated malignancies.

摘要

葡萄膜黑色素瘤 (UM) 是眼部最常见的原发性眼内恶性肿瘤。它具有很高的转移潜能,主要转移到肝脏。遗传学在肿瘤分类和 UM 转移性疾病的预后中起着至关重要的作用。在转移的 UM 中发生突变的驱动基因之一是剪接因子 3b 的亚基 1 (),它是剪接体复合物的一个组成部分。在 UM 和其他恶性肿瘤中观察到剪接体复合物成分的复发性突变,这表明它们在肿瘤发生中起着重要作用。是最常见的突变剪接体基因,在 UM 中与晚期转移相关。本综述总结了 UM 中剪接体突变的遗传和表观遗传见解。它们构成了 UM 的一个独特亚组,与其他剪接体突变的恶性肿瘤具有相似性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11b9/7765440/59c134fbfbfb/ijms-21-09546-g001.jpg

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