Applications of CRISPR-Cas9 Technology in Translational Research on Solid-Tumor Cancers

Patricia Chen1,2, Liting You1, You Lu1

  • 11 Department of Thoracic Oncology, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China .

The CRISPR Journal
|April 26, 2019
PubMed

Insights

CRISPR-Cas9 gene editing is advancing disease modeling and research. This review explores its current and future uses in solid tumor research and clinical applications, alongside challenges.

Area of Science:

  • Biomedical research
  • Genomics
  • Cancer biology

Background:

  • CRISPR-Cas9 has revolutionized genome editing since its inception.
  • Its applications span disease modeling, gene-phenotype studies, and therapeutic interventions.
  • While primarily used in basic research, translation to clinical settings is progressing.

Purpose of the Study:

  • To review current and prospective applications of CRISPR-Cas9 in solid tumor research.
  • To examine the translational potential of CRISPR-Cas9 from laboratory to clinical practice.
  • To identify challenges associated with implementing CRISPR-Cas9 in clinical settings for solid tumors.

Main Methods:

  • Literature review of CRISPR-Cas9 applications in solid tumor research.
  • Analysis of ongoing translational studies and clinical trials.
  • Discussion of technical, ethical, and regulatory hurdles.

Main Results:

  • CRISPR-Cas9 is instrumental in creating sophisticated preclinical models of solid tumors.
  • The system shows promise for targeted cancer therapies and diagnostics.
  • Significant challenges remain in delivery, specificity, and long-term safety for clinical use.

Conclusions:

  • CRISPR-Cas9 holds immense potential for advancing solid tumor research and treatment.
  • Bridging the gap between basic research and clinical application requires overcoming key obstacles.
  • Continued innovation is crucial for realizing the full therapeutic benefits of CRISPR-Cas9 in oncology.

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