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In Vitro Selection of Engineered Transcriptional Repressors for Targeted Epigenetic Silencing
Published on: May 5, 2023
Potential Therapeutics Targeting Upstream Regulators and Interactors of EHMT1/2
Gareth Chin Khye Ang1,2,3, Amogh Gupta1, Uttam Surana2,3
1Healthy Longevity Translational Research Program, Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117593, Singapore.
Abstract:
Euchromatin histone lysine methyltransferases (EHMTs) are epigenetic regulators responsible for silencing gene transcription by catalyzing H3K9 dimethylation. Dysregulation of EHMT1/2 has been reported in multiple cancers and is associated with poor clinical outcomes. Although substantial insights have been gleaned into the downstream targets and pathways regulated by EHMT1/2, few studies have uncovered mechanisms responsible for their dysregulated expression. Moreover, EHMT1/2 interacting partners, which can influence their function and, therefore, the expression of target genes, have not been extensively explored. As none of the currently available EHMT inhibitors have made it past clinical trials, understanding upstream regulators and EHMT protein complexes may provide unique insights into novel therapeutic avenues in EHMT-overexpressing cancers. Here, we review our current understanding of the regulators and interacting partners of EHMTs. We also discuss available therapeutic drugs that target the upstream regulators and binding partners of EHMTs and could potentially modulate EHMT function in cancer progression.
Insights
Euchromatin histone lysine methyltransferases (EHMTs) regulate gene silencing. Understanding EHMT regulators and interacting proteins offers new therapeutic strategies for cancers with EHMT dysregulation.
Area of Science:
- Epigenetics
- Cancer Biology
- Molecular Oncology
Background:
- Euchromatin histone lysine methyltransferases (EHMTs) catalyze H3K9 dimethylation, silencing gene transcription.
- Dysregulated EHMT1/2 expression is linked to poor outcomes in various cancers.
- Mechanisms driving EHMT1/2 dysregulation and their interacting partners remain underexplored.
Purpose of the Study:
- To review current knowledge on EHMT regulators and interacting partners.
- To explore potential therapeutic strategies targeting EHMTs in cancer.
Main Methods:
- Literature review of EHMT function, regulation, and interactions.
- Analysis of existing therapeutic agents targeting EHMT pathways.
Main Results:
- EHMT1/2 dysregulation is implicated in cancer progression.
- Interacting partners influence EHMT function and target gene expression.
- Limited success of current EHMT inhibitors necessitates alternative approaches.
Conclusions:
- Understanding EHMT upstream regulators and protein complexes is crucial for novel cancer therapies.
- Targeting EHMT regulators and binding partners may offer new avenues for EHMT-overexpressing cancers.
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