CRISPR-Cas and CRISPR-based screening system for precise gene editing and targeted cancer therapy

Mingming Qin1,2, Chunhao Deng3, Liewei Wen4

  • 1Reproductive Medical Center, Affiliated Foshan Maternity & Child Healthcare Hospital, Southern Medical University (Foshan Women and Children Hospital), Foshan, Guangdong, 528000, China.

Insights

CRISPR-Cas systems enable precise genetic modification for cancer research and therapy. This review details CRISPR screening applications in CAR-T cell therapy and drug development for improved cancer treatment.

Area of Science:

  • Molecular Biology
  • Genetics
  • Oncology

Background:

  • CRISPR-Cas systems have revolutionized molecular biology and cancer research.
  • These systems are crucial for genetic investigation and precision cancer therapy.

Purpose of the Study:

  • To review CRISPR-Cas and CRISPR screening systems in cancer research.
  • To discuss applications in CAR-T cell therapy, drug targeting, and screening.
  • To explore CRISPR's advantages, obstacles, and future in precision medicine.

Main Methods:

  • Summarizing genetic modification techniques using CRISPR/Cas.
  • Analyzing key components for CRISPR screening (Cas enzymes, gRNA libraries, target cells).
  • Reviewing applications in ex vivo and in vivo settings for CAR-T therapy and drug development.

Main Results:

  • CRISPR screening facilitates CAR-T cell therapy optimization.
  • It aids in identifying drug targets and screening potential therapeutics.
  • CRISPR systems offer significant advantages for precision cancer medicine.

Conclusions:

  • CRISPR/Cas and screening systems are vital tools for advancing cancer therapy.
  • Further development promises enhanced precision and accuracy in individualized gene therapy.
  • Overcoming obstacles will unlock the full potential of CRISPR in clinical settings.

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