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Spliceosome Mutations in Uveal Melanoma.
- 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.
- Subjects :
- Amino Acid Substitution
Exons
Gene Frequency
Humans
Melanoma metabolism
Melanoma mortality
Melanoma pathology
Phosphoproteins chemistry
Phosphoproteins genetics
Phosphoproteins metabolism
RNA Splicing
RNA Splicing Factors chemistry
RNA Splicing Factors metabolism
Spliceosomes
Telomere genetics
Uveal Neoplasms metabolism
Uveal Neoplasms mortality
Uveal Neoplasms pathology
Melanoma genetics
Mutation
RNA Splicing Factors genetics
Uveal Neoplasms genetics
Subjects
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