Related Experiment Video
Updated: Feb 7, 2026

CRISPR/Cas9 Ribonucleoprotein-mediated Precise Gene Editing by Tube Electroporation
Published on: June 20, 2019
CRISPR-Cas9 therapies in experimental mouse models of cancer
Diogo Estêvão1,2, Natália Rios Costa1, Rui Gil da Costa3,4
1Molecular Oncology & Viral Pathology Group, IPO Porto Research Center (CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto), 4200-072 Porto, Portugal Porto, Portugal.
Abstract:
The CRISPR-Cas9, a part of the defence mechanism from bacteria, has rapidly become the simplest, fastest and the most precise genome-editing tool available. The therapeutic applications of CRISPR are boundless: correction of mutations in several disorders, inactivation of oncogenes and viral oncoproteins, and activation of tumor suppressor genes. In this review, we expose recent advances concerning animal models of cancer that use CRISPR-Cas9, addressing also the current efforts to develop CRISPR-Cas9-based therapies, focusing on proof-of-concept studies. Finally, the review exposes some of the main challenges that this genome-editing tool faces. The key issue remains: does CRISPR-Cas9 have real potential for therapeutic application or will it just remain a wonderful research tool?
Insights
CRISPR-Cas9 gene editing offers vast therapeutic potential for cancer, with recent advances in animal models and proof-of-concept studies. Challenges remain in translating this powerful research tool into clinical applications.
Area of Science:
- Biotechnology
- Genetics
- Molecular Biology
Background:
- CRISPR-Cas9 is a bacterial defense mechanism repurposed as a precise genome-editing tool.
- Its applications include correcting mutations, inactivating oncogenes, and activating tumor suppressor genes.
Purpose of the Study:
- To review recent advances in CRISPR-Cas9 applications for animal cancer models.
- To discuss the development of CRISPR-Cas9-based therapies and proof-of-concept studies.
- To identify challenges facing CRISPR-Cas9 as a therapeutic tool.
Main Methods:
- Review of recent scientific literature on CRISPR-Cas9 in cancer research.
- Analysis of proof-of-concept studies for CRISPR-Cas9-based therapies.
- Discussion of challenges and future potential.
Main Results:
- CRISPR-Cas9 is a highly precise and efficient genome-editing technology.
- Significant progress has been made in utilizing CRISPR-Cas9 in animal cancer models.
- Proof-of-concept studies show promise for CRISPR-Cas9-based cancer therapies.
Conclusions:
- CRISPR-Cas9 demonstrates substantial potential for cancer therapy development.
- Further research is needed to overcome challenges and realize its full therapeutic application.
- The key question is whether CRISPR-Cas9 will transition from a research tool to a clinical reality.
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...
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Targeted Cancer Therapies
There are several types of targeted therapies against...
Mouse Models of Cancer Study
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...

