Related Experiment Video
Updated: Sep 14, 2025

Using CRISPR/Cas9 Gene Editing to Investigate the Oncogenic Activity of Mutant Calreticulin in Cytokine Dependent Hematopoietic Cells
Published on: January 5, 2018
CRISPR/Cas9 technology in tumor research and drug development application progress and future prospects
Han Han1, Xiaoyan Sun2, Xiaoyun Guo2
1Department of Biochemistry and Molecular Biology, School of Basic Medicine, Shenyang Medical College, Shenyang, Liaoning, China.
CRISPR/Cas9 gene editing offers powerful tools for cancer research and drug development by enabling precise genome modifications. Despite its potential, challenges like off-target effects and delivery systems need addressing for clinical translation.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- The CRISPR/Cas9 system, a bacterial defense mechanism, has been adapted for precise DNA manipulation.
- This technology utilizes guide RNA and Cas9 endonuclease for targeted gene editing (knockout/knock-in).
Purpose of the Study:
- To review the progress and future prospects of CRISPR/Cas9 technology in oncology research.
- To detail its applications in tumor genome editing, drug target screening, and new drug development.
Main Methods:
- Review of CRISPR/Cas9 applications in cancer biology, including gene transcription and epigenetic editing.
- Discussion of its use in anticancer drug discovery, target identification, and screening strategies.
- Exploration of multimodal functional genomics integration and overcoming CAR-T resistance.
Main Results:
- CRISPR/Cas9 shows significant potential in tumor research, drug development, and personalized therapy.
- It facilitates precise genome engineering, target discovery, and screening for drug resistance mechanisms.
Conclusions:
- CRISPR/Cas9 technology is fundamental to advancing cancer biology and drug discovery.
- Technical challenges (off-target effects, efficiency) and ethical considerations require further research for clinical translation.
Related Concept Videos
CRISPR
CRISPR/Cas9 Genome Editing
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...
Homologous Recombination
Targeted Cancer Therapies
There are several types of targeted therapies against...

