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Updated: Jun 24, 2025

An Integrated Platform for Genome-wide Mapping of Chromatin States Using High-throughput ChIP-sequencing in Tumor Tissues
Published on: April 5, 2018
Chromatin as an old and new anticancer target
Jacques Neefjes1, Katerina Gurova2, Jay Sarthy3
1Department of Cell and Chemical Biology and Oncode Institute, LUMC, Einthovenweg 20, 2333, ZC, Leiden, The Netherlands.
Chromatin modifiers are frequently mutated in cancer, yet DNA-damaging chemotherapies are standard. This review introduces 'chromatin damage' from small molecules, like anthracyclines, suggesting new cancer treatment strategies.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Chromatin modifiers are frequently mutated in various cancers.
- Current cancer treatments often target DNA damage, despite mutations in chromatin regulators.
- A gap exists in treating cancers with chromatin-related genetic alterations.
Purpose of the Study:
- To introduce the concept of 'chromatin damage' as a therapeutic target.
- To highlight overlooked chromatin-targeting chemotherapeutic agents.
- To explore novel chromatin-damaging agents for cancer treatment.
Main Methods:
- Review of existing literature on chromatin modifiers and cancer.
- Analysis of small molecules that induce non-genetic damage to protein-DNA interactions.
- Focus on anthracyclines as a case study for chromatin-targeting agents.
Main Results:
- Established the concept of 'chromatin damage' distinct from DNA damage.
- Identified anthracyclines as clinically relevant chromatin-damaging agents.
- Highlighted the potential of overlooked chromatin-targeting therapies.
Conclusions:
- 'Chromatin damage' represents a new paradigm for cancer therapy.
- Anthracyclines and similar agents offer therapeutic avenues for chromatin-deranged cancers.
- Further research into chromatin-damaging agents can improve cancer treatment outcomes.
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