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Alternative mechanisms of miR-34a regulation in cancer
E. Slabáková, Z. Culig, J. Remšík, K. Souček,
Language English Country England, Great Britain
Document type Journal Article, Review
Grant support
NV15-33999A
MZ0
CEP Register
NV15-28628A
MZ0
CEP Register
Digital library NLK
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Full text - Article
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- MeSH
- Epigenesis, Genetic genetics MeSH
- Epithelial-Mesenchymal Transition genetics MeSH
- Humans MeSH
- MicroRNAs genetics MeSH
- Tumor Suppressor Protein p53 genetics MeSH
- Neoplasms genetics pathology MeSH
- Promoter Regions, Genetic genetics MeSH
- Gene Expression Regulation, Neoplastic genetics MeSH
- Genes, Tumor Suppressor * MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
MicroRNA miR-34a is recognized as a master regulator of tumor suppression. The strategy of miR-34a replacement has been investigated in clinical trials as the first attempt of miRNA application in cancer treatment. However, emerging outcomes promote the re-evaluation of existing knowledge and urge the need for better understanding the complex biological role of miR-34a. The targets of miR-34a encompass numerous regulators of cancer cell proliferation, survival and resistance to therapy. MiR-34a expression is transcriptionally controlled by p53, a crucial tumor suppressor pathway, often disrupted in cancer. Moreover, miR-34a abundance is fine-tuned by context-dependent feedback loops. The function and effects of exogenously delivered or re-expressed miR-34a on the background of defective p53 therefore remain prominent issues in miR-34a based therapy. In this work, we review p53-independent mechanisms regulating the expression of miR-34a. Aside from molecules directly interacting with MIR34A promoter, processes affecting epigenetic regulation and miRNA maturation are discussed. Multiple mechanisms operate in the context of cancer-associated phenomena, such as aberrant oncogene signaling, EMT or inflammation. Since p53-dependent tumor-suppressive mechanisms are disturbed in a substantial proportion of malignancies, we summarize the effects of miR-34a modulation in cell and animal models in the clinically relevant context of disrupted or insufficient p53 function.
References provided by Crossref.org
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