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The Regulatory Network of hnRNPs Underlying Regulating PKM Alternative Splicing in Tumor Progression.
- Source :
-
Biomolecules [Biomolecules] 2024 May 09; Vol. 14 (5). Date of Electronic Publication: 2024 May 09. - Publication Year :
- 2024
-
Abstract
- One of the hallmarks of cancer is metabolic reprogramming in tumor cells, and aerobic glycolysis is the primary mechanism by which glucose is quickly transformed into lactate. As one of the primary rate-limiting enzymes, pyruvate kinase (PK) M is engaged in the last phase of aerobic glycolysis. Alternative splicing is a crucial mechanism for protein diversity, and it promotes PKM precursor mRNA splicing to produce PKM2 dominance, resulting in low PKM1 expression. Specific splicing isoforms are produced in various tissues or illness situations, and the post-translational modifications are linked to numerous disorders, including cancers. hnRNPs are one of the main components of the splicing factor families. However, there have been no comprehensive studies on hnRNPs regulating PKM alternative splicing. Therefore, this review focuses on the regulatory network of hnRNPs on PKM pre-mRNA alternative splicing in tumors and clinical drug research. We elucidate the role of alternative splicing in tumor progression, prognosis, and the potential mechanism of abnormal RNA splicing. We also summarize the drug targets retarding tumorous splicing events, which may be critical to improving the specificity and effectiveness of current therapeutic interventions.
- Subjects :
- Humans
Disease Progression
Gene Expression Regulation, Neoplastic
Animals
Alternative Splicing genetics
Neoplasms genetics
Neoplasms pathology
Neoplasms metabolism
Heterogeneous-Nuclear Ribonucleoproteins metabolism
Heterogeneous-Nuclear Ribonucleoproteins genetics
Pyruvate Kinase genetics
Pyruvate Kinase metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2218-273X
- Volume :
- 14
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Biomolecules
- Publication Type :
- Academic Journal
- Accession number :
- 38785973
- Full Text :
- https://doi.org/10.3390/biom14050566