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葡萄膜黑色素瘤的遗传学与RNA调控

Genetics and RNA Regulation of Uveal Melanoma.

作者信息

Barbagallo Cristina, Stella Michele, Broggi Giuseppe, Russo Andrea, Caltabiano Rosario, Ragusa Marco

机构信息

Department of Biomedical and Biotechnological Sciences-Section of Biology and Genetics, University of Catania, 95123 Catania, Italy.

Department of Medical, Surgical Sciences and Advanced Technologies G.F. Ingrassia-Section of Anatomic Pathology, University of Catania, 95123 Catania, Italy.

出版信息

Cancers (Basel). 2023 Jan 26;15(3):775. doi: 10.3390/cancers15030775.

Abstract

Uveal melanoma (UM) is the most common intraocular malignant tumor and the most frequent melanoma not affecting the skin. While the rate of UM occurrence is relatively low, about 50% of patients develop metastasis, primarily to the liver, with lethal outcome despite medical treatment. Notwithstanding that UM etiopathogenesis is still under investigation, a set of known mutations and chromosomal aberrations are associated with its pathogenesis and have a relevant prognostic value. The most frequently mutated genes are , and , with mutually exclusive mutations occurring in and , and almost mutually exclusive ones in and , and and . Among chromosomal aberrations, monosomy of chromosome 3 is the most frequent, followed by gain of chromosome 8q, and full or partial loss of chromosomes 1 and 6. In addition, epigenetic mechanisms regulated by non-coding RNAs (ncRNA), namely microRNAs and long non-coding RNAs, have also been investigated. Several papers investigating the role of ncRNAs in UM have reported that their dysregulated expression affects cancer-related processes in both in vitro and in vivo models. This review will summarize current findings about genetic mutations, chromosomal aberrations, and ncRNA dysregulation establishing UM biology.

摘要

葡萄膜黑色素瘤(UM)是最常见的眼内恶性肿瘤,也是最常发生的非皮肤黑色素瘤。虽然UM的发病率相对较低,但约50%的患者会发生转移,主要转移至肝脏,尽管接受了治疗,仍会导致致命后果。尽管UM的病因发病机制仍在研究中,但一组已知的突变和染色体畸变与其发病机制相关,并具有重要的预后价值。最常发生突变的基因是 , , ,在 与 、 与 、 与 中发生相互排斥的突变。在染色体畸变中,3号染色体单体性最为常见,其次是8q染色体增加,以及1号和6号染色体的全部或部分缺失。此外,由非编码RNA(ncRNA),即微小RNA和长链非编码RNA调节的表观遗传机制也已得到研究。几篇研究ncRNA在UM中作用的论文报道,它们表达失调会影响体外和体内模型中与癌症相关的过程。本综述将总结目前关于基因突变、染色体畸变和ncRNA失调建立UM生物学的研究结果。

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