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Published on: January 20, 2019
Histone Modifications and Their Targeting in Lymphoid Malignancies.
Miranda Fernández-Serrano1,2, René Winkler3, Juliana C Santos1
1Lymphoma Translational Group, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain.
Somatic mutations in B cells drive lymphoid neoplasms by altering epigenetic machinery, leading to transcriptional changes. Epigenetic drugs targeting histone modifications show promise for treating B-cell lymphomas.
Area of Science:
- Oncology
- Epigenetics
- Hematology
Background:
- Malignant transformation in lymphoid neoplasms involves somatic mutations affecting B-cell epigenetic machinery.
- Histone modification alterations drive disease-specific transcriptional programs in B-cell lymphomas.
- These changes impact cell cycle regulation, apoptosis, and DNA damage response, promoting immune evasion and lymphoma development.
Purpose of the Study:
- To review epigenetic alterations in B-cell non-Hodgkin lymphoma.
- To present the current state of preclinical and clinical development of epigenetic drugs for lymphoma.
- To focus on therapeutic strategies targeting histone methylation and acetylation.
Main Methods:
- Literature review of epigenetic alterations in B-cell non-Hodgkin lymphoma.
- Analysis of preclinical and clinical data for epigenetic drug development.
- Focus on histone methyltransferase and deacetylase inhibitors.
Main Results:
- Epigenetic alterations are key drivers in B-cell lymphoma pathogenesis.
- Numerous epigenetic drugs are in preclinical and clinical development.
- Targeting histone methylation and acetylation represents a promising therapeutic avenue.
Conclusions:
- Epigenetic dysregulation is central to B-cell lymphoma.
- Epigenetic therapies, particularly those targeting histone modifications, offer significant potential for improving patient outcomes.
- Further development and clinical translation of these therapies are crucial for lymphoma treatment.
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