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Epigenetic targets in B- and T-cell lymphomas: latest developments
Marcelo Lima Ribeiro1,2, Salvador Sánchez Vinces2, Laura Mondragon3
1Lymphoma Translational Group, Josep Carreras Leukaemia Research Institute, Badalona, Spain.
Epigenetic dysregulations are common in Non-Hodgkin's lymphomas (NHLs). Targeting these epigenetic alterations with novel drugs offers promising therapeutic strategies for relapsed or refractory cases.
Area of Science:
- Oncology
- Epigenetics
- Hematology
Background:
- Non-Hodgkin's lymphomas (NHLs) are diverse lymphoid malignancies with varied molecular and clinical features.
- While many NHLs respond to conventional treatments, relapsed/refractory cases have poor outcomes.
- Epigenetic dysregulations, including mutations in epigenetic enzymes, are prevalent in both B-cell and T-cell lymphomas.
Purpose of the Study:
- To summarize key epigenetic alterations in B- and T-cell NHLs.
- To review the development and clinical application of epigenetic-modifying agents (epidrugs) for NHLs.
- To explore future research directions and the role of bioinformatics in identifying new epigenetic targets.
Main Methods:
- Review of scientific literature on epigenetic alterations in NHLs.
- Analysis of clinical trial data for approved and investigational epidrugs.
- Discussion of bioinformatics approaches for target discovery.
Main Results:
- Epigenetic alterations are frequently observed in NHLs, impacting chromatin modifiers and DNA methyltransferases (DNMTs).
- Several classes of epidrugs, including DNMT, histone deacetylase (HDAC), and bromodomain and extra-terminal motif (BET) inhibitors, are under clinical investigation or approved.
- These agents show potential in treating specific NHL subtypes.
Conclusions:
- Epigenetic modifications represent a critical area for therapeutic intervention in NHL.
- Targeted epigenetic therapies, informed by deep sequencing and bioinformatics, hold promise for improving outcomes in relapsed/refractory NHL.
- Further research is needed to fully elucidate the role of epigenetics and optimize epidrug strategies.
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