Related Experiment Video
Updated: Sep 6, 2025

08:32
Genome-Wide CRISPR Screen for Unveiling Radiosensitive and Radioresistant Genes
Published on: May 23, 2025
447
CRISPR: A Promising Tool for Cancer Therapy
Fatemeh Mohammad-Rafiei1, Esmat Safdarian2, Bashir Adel3
1Department of Medical Biotechnology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Current Molecular Medicine
|June 24, 2022
Summary
The CRISPR-Cas system, a powerful genome editing tool, revolutionizes genetic research and medical treatments. Its precision and ease of use are transforming fields from basic science to targeted cancer therapies.
Area of Science:
- Molecular Biology
- Genetics
- Biotechnology
Background:
- The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) system represents a significant advancement in genome editing technology.
- CRISPR technology is rapidly surpassing older methods like zinc-finger nucleases (ZFNs) due to its efficiency and accuracy.
- Its applications span fundamental scientific research, medical studies, and therapeutic interventions.
Approach:
- The CRISPR-Cas system comprises two essential components: a CRISPR-associated (Cas) nuclease for DNA binding and cleavage, and a guide ribonucleic acid (gRNA) for target site specificity.
- This system enables precise manipulation of genetic material.
- The review focuses on the integration and impact of CRISPR/Cas systems in various research applications, including epigenome modification and genome-wide screening.
Key Points:
- CRISPR/Cas systems offer unprecedented precision in genome editing.
- The technology has diverse applications, including gene editing, epigenome modifications, and genome-wide screening.
- CRISPR is increasingly vital in developing targeted cancer therapies.
Conclusions:
- CRISPR/Cas systems have revolutionized genome editing across scientific disciplines.
- The technology's versatility supports a wide range of applications, from basic research to clinical treatments.
- Further research into CRISPR/Cas systems holds significant promise for advancing cancer therapy and other medical fields.
Related Concept Videos
CRISPR
52.8K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
52.8K
CRISPR/Cas9 Genome Editing
204
The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
204
CRISPR and crRNAs
17.3K
Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
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...
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...
17.3K
Homologous Recombination
51.2K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
51.2K
Targeted Cancer Therapies
7.8K
The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
There are several types of targeted therapies against...
7.8K

