Related Experiment Video
Updated: Jan 25, 2026

Construction of Homozygous Mutants of Migratory Locust Using CRISPR/Cas9 Technology
Published on: March 16, 2022
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 .
Abstract:
Since its introduction to genome editing, CRISPR-Cas9 has been used to generate cell and animal models of disease, investigate relations between genomes and phenotypes, and interfere with disease development. Although most of its applications have been in basic research, efforts are underway to move CRISPR-Cas9 from bench to bedside. This review summarizes current and prospective applications of the CRISPR-Cas9 system in biomedical and translational research on solid tumors, as well as the challenges of expanding this technology into clinical use.
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.
Related Concept Videos
CRISPR
CRISPR and crRNAs
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
CRISPR/Cas9 Genome Editing
Translation
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of...
Metallic Solids
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
Structures of Solids

