10 papers analyzed
Some studies suggest CRISPR gene editing has potential benefits for treating genetic disorders, cancer, and infectious diseases, while other studies highlight risks such as off-target changes, cancer-causing genes, social harms, and biosecurity concerns.
CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a groundbreaking gene-editing technology that has the potential to revolutionize medicine by enabling precise modifications to DNA. This technology holds promise for treating a wide range of diseases, but it also comes with potential risks and ethical concerns.
Therapeutic Potential and Disease Treatment:
Cancer Treatment:
Infectious Diseases and Global Health Security:
Biosecurity and Ethical Concerns:
Health Equity and Public Health:
Technical and Safety Challenges:
CRISPR technology holds immense potential for treating a variety of diseases and improving global health security. However, it also presents significant ethical, biosecurity, and technical challenges that need to be addressed. Ensuring equitable access and minimizing risks will be crucial for the responsible development and application of CRISPR in medicine.
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