CRISPR/Cas9 in CSC Research
CRISPR/Cas9 technology has revolutionized cancer research, providing a powerful tool to edit genes and study their functions in cancer stem cells (CSCs). This track focuses on how CRISPR/Cas9 is being used to investigate the genetic and epigenetic regulation of CSCs, identify novel therapeutic targets, and test potential drug candidates. Researchers use CRISPR to knock out specific genes involved in CSC self-renewal, survival, and therapy resistance, revealing new insights into CSC biology. This cutting-edge research aims to develop gene-editing strategies that selectively target CSCs, offering a highly specific approach to eradicating the cells responsible for cancer progression and relapse.
Related Conference of CRISPR/Cas9 in CSC Research
April 21-22, 2025
16th International Conference on Cancer Stem Cell & Oncology Research
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October 13-14, 2025
8th International Conference on Anti-Cancer Drugs & Therapies
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CRISPR/Cas9 in CSC Research Conference Speakers
Recommended Sessions
- CRISPR/Cas9 in CSC Research
- CSC and Immunoediting
- CSC Biomarkers for Early Detection
- CSC Fate Determination and Differentiation
- CSC Heterogeneity in Tumors
- CSC Metabolism and Energy Pathways
- CSC Niche and Hypoxia
- CSC Plasticity and Tumor Progression
- CSC-Derived Exosomes and Communication
- CSC-Driven Angiogenesis
- CSC-Driven Resistance to Radiotherapy
- CSC-Mediated Immunosuppression
- CSCs and Tumor Microenvironment
- Drug Resistance Mechanisms in CSCs
- Epigenetics and CSC Regulation
- Immunotherapy and CSCs
- Inflammation and CSC Activation
- Molecular Signaling in CSCs
- Nanotechnology and CSC Targeting
- Natural Products and CSC Targeting
- Role of CSCs in Metastasis
- Role of EMT in CSC Plasticity
- Targeting CSC Dormancy
- Targeting CSC-Specific Surface Markers
- Therapy Resistance and CSCs
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