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Updated: Jan 16, 2026

Engineering Oncogenic Heterozygous Gain-of-Function Mutations in Human Hematopoietic Stem and Progenitor Cells
Published on: March 10, 2023
Gene editing techniques in cancer research
Nurhasni Hasan1, Juliana Palungan1, Muneeb Ullah2
1Faculty of Pharmacy, Universitas Hasanuddin, Jl. Perintis Kemerdekaan Km 10, Makassar, Indonesia.
Abstract:
The process of editing genes has emerged as a game-changing instrument in the field of cancer research. It has the potential to provide a whole new understanding of the biology of tumors and to facilitate the creation of tailored medicines. Zinc finger nucleases (ZFNs), transcription activator-like effector nucleases (TALENs), and the clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system are the three basic methods of gene editing techniques that are discussed in this chapter. We investigate the protocol modifications that are specific to each approach, focusing on high-prevalence tumors, and we investigate the utility, efficiency, and application issues that are associated with each technique in oncology. In addition, we describe current developments in improving these methods to successfully target oncogenes and tumor suppressor genes, with the goal of driving forward advances in precision cancer therapy.
Insights
Gene editing technologies like CRISPR-Cas9 offer new ways to understand tumors and develop personalized cancer therapies. This research explores methods, challenges, and advancements in applying gene editing to target cancer-causing genes.
Area of Science:
- Oncology
- Genetics
- Biotechnology
Background:
- Gene editing is revolutionizing cancer research by offering insights into tumor biology.
- It holds promise for developing targeted cancer medicines and therapies.
- Understanding different gene editing techniques is crucial for advancing cancer treatment.
Purpose of the Study:
- To review and compare major gene editing techniques: Zinc Finger Nucleases (ZFNs), Transcription Activator-Like Effector Nucleases (TALENs), and CRISPR-Cas9.
- To analyze protocol modifications, utility, efficiency, and application challenges of these methods in high-prevalence tumors.
- To discuss current advancements in targeting oncogenes and tumor suppressor genes for precision cancer therapy.
Main Methods:
- Comparative analysis of ZFNs, TALENs, and CRISPR-Cas9 systems.
- Review of protocol modifications specific to different tumor types.
- Examination of efficiency, utility, and application challenges in oncology.
Main Results:
- Detailed discussion on the specific protocols and modifications for each gene editing technique.
- Evaluation of the effectiveness and limitations of ZFNs, TALENs, and CRISPR-Cas9 in targeting cancer genes.
- Identification of current progress in refining gene editing tools for oncogene and tumor suppressor gene targeting.
Conclusions:
- Gene editing techniques are pivotal in advancing precision cancer therapy.
- Further development is needed to overcome challenges and enhance the application of these tools in oncology.
- These technologies are key to unlocking new therapeutic strategies for various cancers.
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