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Spliceosome Mutations in Uveal Melanoma.

Authors :
Nguyen JQN
Drabarek W
Yavuzyigitoglu S
Medico Salsench E
Verdijk RM
Naus NC
de Klein A
KiliƧ E
Brosens E
Source :
International journal of molecular sciences [Int J Mol Sci] 2020 Dec 15; Vol. 21 (24). Date of Electronic Publication: 2020 Dec 15.
Publication Year :
2020

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 ( SF3B1 ), 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. SF3B1 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.

Details

Language :
English
ISSN :
1422-0067
Volume :
21
Issue :
24
Database :
MEDLINE
Journal :
International journal of molecular sciences
Publication Type :
Academic Journal
Accession number :
33333932
Full Text :
https://doi.org/10.3390/ijms21249546