مقاله علمية للسيدة العميدة الاستاذ المساعد الدكتور زهراء حليم القيم بعنوان " CRISPR-Gene Therapy "

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Revolutionizing Medicine<br /><br />CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) gene therapy is a groundbreaking technology that allows precise editing of DNA to treat genetic disorders. It utilizes the CRISPR-Cas9 system, which acts like molecular “scissors” to cut and modify specific DNA sequences.<br /><br /> 1. Targeting the Gene – A guide RNA (gRNA) is designed to locate the faulty gene sequence.<br /> 2. Cutting the DNA – The Cas9 enzyme cuts the DNA at the targeted site.<br /> 3. Repair or Replacement – The cell’s natural repair mechanisms either disable the faulty gene or insert a correct version.<br /><br />Applications in Medicine<br /><br />CRISPR-based therapies are being explored for treating:<br /> • Genetic disorders (e.g., sickle cell anemia, cystic fibrosis, muscular dystrophy)<br /> • Cancer (enhancing immune cells to fight tumors)<br /> • Infectious diseases (such as HIV and viral infections)<br /> • Blindness (correcting genetic mutations causing inherited blindness)<br /><br />What the Challenges and Ethical Considerations?<br /> • Off-target effects: Accidental DNA modifications could cause unintended consequences.<br /> • Delivery methods: Efficiently delivering CRISPR components into human cells remains a challenge.<br /> • Ethical concerns: Editing germline cells (heritable changes) raises ethical and regulatory debates.<br /><br /> What the Future Prospects<br /><br />Ongoing research aims to improve CRISPR’s precision, safety, and delivery methods, bringing hope for curing previously untreatable diseases. Clinical trials are already demonstrating promising results, making CRISPR-based gene therapy one of the most exciting advancements in modern medicine.<br /><br /><br />CRISPR gene therapy is a vast and exciting fild<br /><br /> CRISPR interested in:<br /> • Clinical applications (specific diseases being treated with CRISPR)<br /> • Mechanism of action (how CRISPR edits genes)<br /> • Recent breakthroughs and clinical trials<br /> • Ethical and regulatory challenges<br /> • Delivery methods and improvements<br />جامعة المستقبل الجامعة الاولى في العراق