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.

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