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An Integrated Platform for Genome-wide Mapping of Chromatin States Using High-throughput ChIP-sequencing in Tumor Tissues
Published on: April 5, 2018
Chromatin Accessibility in Cancer: Biological Functions, Mechanisms, Therapeutic Potential, and Future Directions
Wentao Xia1,2,3,4, Min Jiang1,2,3, Yefei Huang1,2,3
1School of Public Health Xuzhou Medical University Xuzhou Jiangsu China.
Abstract:
Cancer remains a major therapeutic challenge owing to its complex pathogenesis and the limitations of current treatments, such as poor specificity, toxicity, and multidrug resistance. Chromatin accessibility, which is dynamically regulated by genetic, epigenetic, and environmental factors, plays crucial roles in cancer initiation and progression. However, substantial obstacles persist in developing therapeutic strategies that target chromatin accessibility and translating them into clinical practice. This review comprehensively summarizes the biological functions and regulatory mechanisms of chromatin accessibility in tumors, encompassing tumorigenesis, progression, metabolic reprogramming, angiogenesis, stemness, tumor immune microenvironment, and therapy resistance. We integrate comparisons between human and murine models and detail key profiling technologies, including Assay for Transposase‑Accessible Chromatin with high‑throughput sequencing, DNase‑seq, single‑cell multiomics, and three-dimensional chromatin‑conformation assays. Furthermore, we compile recent preclinical and clinical trials that utilize chromatin accessibility as a biomarker or therapeutic target, along with combination strategies involving chemotherapy, immunotherapy, targeted therapy, and radiotherapy. From a multiomics and interdisciplinary perspective, we discuss current limitations in translating fundamental research into clinical applications and highlight future directions for epigenetics‑based precision oncology.
Insights
Chromatin accessibility is key in cancer development and treatment resistance. Targeting it offers new precision oncology strategies, but clinical translation faces challenges.
Area of Science:
- Oncology
- Epigenetics
- Genomics
Background:
- Cancer poses significant therapeutic challenges due to complexity and treatment limitations like resistance and toxicity.
- Chromatin accessibility, influenced by various factors, is critical in cancer initiation and progression.
- Developing effective therapies targeting chromatin accessibility remains a significant hurdle for clinical application.
Purpose of the Study:
- To comprehensively review the biological roles and regulatory mechanisms of chromatin accessibility in tumors.
- To detail key profiling technologies for assessing chromatin accessibility.
- To summarize current clinical trials and combination strategies involving chromatin accessibility, and discuss future directions for epigenetics-based precision oncology.
Main Methods:
- Review of biological functions and regulatory mechanisms of chromatin accessibility in cancer.
- Integration of human and murine model comparisons.
- Detailed examination of profiling technologies: Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq), DNase-seq, single-cell multiomics, and 3D chromatin conformation assays.
- Compilation of preclinical and clinical trials and combination strategies.
Main Results:
- Chromatin accessibility influences tumorigenesis, progression, metabolic reprogramming, angiogenesis, stemness, the tumor immune microenvironment, and therapy resistance.
- Key technologies like ATAC-seq and DNase-seq enable detailed profiling.
- Numerous trials explore chromatin accessibility as a biomarker and therapeutic target, with promising combination strategies.
Conclusions:
- Chromatin accessibility is a pivotal factor in cancer biology and a promising target for novel therapies.
- Significant progress has been made in profiling and targeting chromatin accessibility, with ongoing clinical investigations.
- Overcoming challenges in translating research findings is crucial for advancing epigenetics-based precision oncology.
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