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SMYD family in cancer: epigenetic regulation and molecular mechanisms of cancer proliferation, metastasis, and drug resistance.
- Source :
-
Experimental & molecular medicine [Exp Mol Med] 2024 Nov; Vol. 56 (11), pp. 2325-2336. Date of Electronic Publication: 2024 Nov 01. - Publication Year :
- 2024
-
Abstract
- Epigenetic modifiers (miRNAs, histone methyltransferases (HMTs)/demethylases, and DNA methyltransferases/demethylases) are associated with cancer proliferation, metastasis, angiogenesis, and drug resistance. Among these modifiers, HMTs are frequently overexpressed in various cancers, and recent studies have increasingly identified these proteins as potential therapeutic targets. In this review, we discuss members of the SET and MYND domain-containing protein (SMYD) family that are topics of extensive research on the histone methylation and nonhistone methylation of cancer-related genes. Various members of the SMYD family play significant roles in cancer proliferation, metastasis, and drug resistance by regulating cancer-specific histone methylation and nonhistone methylation. Thus, the development of specific inhibitors that target SMYD family members may lead to the development of cancer treatments, and combination therapy with various anticancer therapeutic agents may increase treatment efficacy.<br />Competing Interests: Competing interests: The authors declare no competing interests.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Animals
Neoplasm Metastasis
Histone-Lysine N-Methyltransferase metabolism
Histone-Lysine N-Methyltransferase genetics
Antineoplastic Agents pharmacology
Antineoplastic Agents therapeutic use
Histones metabolism
Histone Demethylases metabolism
Histone Demethylases genetics
Histone Demethylases antagonists & inhibitors
Neoplasms genetics
Neoplasms drug therapy
Neoplasms pathology
Neoplasms metabolism
Epigenesis, Genetic
Drug Resistance, Neoplasm genetics
Gene Expression Regulation, Neoplastic drug effects
Cell Proliferation drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 2092-6413
- Volume :
- 56
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Experimental & molecular medicine
- Publication Type :
- Academic Journal
- Accession number :
- 39482529
- Full Text :
- https://doi.org/10.1038/s12276-024-01326-8