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Splice factor mutations and alternative splicing as drivers of hematopoietic malignancy.
- Source :
-
Immunological reviews [Immunol Rev] 2015 Jan; Vol. 263 (1), pp. 257-78. - Publication Year :
- 2015
-
Abstract
- Differential splicing contributes to the vast complexity of mRNA transcripts and protein isoforms that are necessary for cellular homeostasis and response to developmental cues and external signals. The hematopoietic system provides an exquisite example of this. Recently, discovery of mutations in components of the spliceosome in various hematopoietic malignancies (HMs) has led to an explosion in knowledge of the role of splicing and splice factors in HMs and other cancers. A better understanding of the mechanisms by which alternative splicing and aberrant splicing contributes to the leukemogenic process will enable more efficacious targeted approaches to tackle these often difficult to treat diseases. The clinical implications are only just starting to be realized with novel drug targets and therapeutic strategies open to exploitation for patient benefit.<br /> (© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Subjects :
- Animals
Carcinogenesis genetics
Hematologic Neoplasms drug therapy
Humans
Molecular Targeted Therapy
Mutation genetics
Protein Isoforms genetics
Protein Isoforms metabolism
RNA Splice Sites genetics
RNA Splicing Factors
Serine-Arginine Splicing Factors
Splicing Factor U2AF
Alternative Splicing genetics
Hematologic Neoplasms genetics
Nuclear Proteins genetics
Phosphoproteins genetics
RNA, Messenger genetics
Ribonucleoprotein, U2 Small Nuclear genetics
Ribonucleoproteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1600-065X
- Volume :
- 263
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Immunological reviews
- Publication Type :
- Academic Journal
- Accession number :
- 25510282
- Full Text :
- https://doi.org/10.1111/imr.12241