دورية أكاديمية
CRISPR-Based Approaches for Cancer Immunotherapy.
| العنوان: | CRISPR-Based Approaches for Cancer Immunotherapy. |
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| المؤلفون: | Malla RR; Cancer Biology Laboratory, Department of Biochemistry and Bioinformatics, School of Science, Gandhi Institute of Technology and Management (GITAM) (Deemed to be University), Visakhapatnam-530045, Andhra Pradesh, India; Department of Biochemistry and Bioinformatics, School of Science, GITAM (Deemed to be University), Visakhapatnam-530045, Andhra Pradesh, India., Middela K; Department of Biochemistry and Bioinformatics, School of Science, GITAM (Deemed to be University), Visakhapatnam-530045, Andhra Pradesh, India. |
| المصدر: | Critical reviews in oncogenesis [Crit Rev Oncog] 2023; Vol. 28 (4), pp. 1-14. |
| نوع المنشور: | Review; Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Begell House Country of Publication: United States NLM ID: 8914610 Publication Model: Print Cited Medium: Internet ISSN: 0893-9675 (Print) Linking ISSN: 08939675 NLM ISO Abbreviation: Crit Rev Oncog Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: New York, NY : Begell House Original Publication: [Boca Raton, FL : CRC Press, c1989- |
| مواضيع طبية MeSH: | CRISPR-Cas Systems*/genetics , Neoplasms*/genetics , Neoplasms*/therapy, Humans ; Gene Editing ; Immunotherapy ; DNA |
| مستخلص: | Clustered regularly interspaced short palindromic repeats (CRISPR) technology is a powerful gene editing tool that has the potential to revolutionize cancer treatment. It allows for precise and efficient editing of specific genes that drive cancer growth and progression. CRISPR-based approaches gene knock-out, which deletes specific genes or sequences of DNA within a cancer cell, and gene knock-in, which inserts new sequences of DNA into a cancer cell to identify potential targets for cancer therapy. Further, genome-wide CRISPR-Cas9-based screens identify specific markers for diagnosis of cancers. Recently, immunotherapy has become a highly efficient strategy for the treatment of cancer. The use of CRISPR in cancer immunotherapy is focused on enhancing the function of T cells, making them more effective at attacking cancer cells and inactivating the immune evasion mechanisms of cancer cells. It has the potential to generate CAR-T cells, which are T cells that have been genetically engineered to target and attack cancer cells specifically. This review uncovers the latest developments in CRISPR-based gene editing strategies and delivery of their components in cancer cells. In addition, the applications of CRISPR in cancer immune therapy are discussed. Overall, this review helps to explore the potential of CRISPR-based strategies in cancer immune therapy in clinical settings. |
| المشرفين على المادة: | 9007-49-2 (DNA) |
| تواريخ الأحداث: | Date Created: 20231205 Date Completed: 20231207 Latest Revision: 20231207 |
| رمز التحديث: | 20240628 |
| DOI: | 10.1615/CritRevOncog.2023048723 |
| PMID: | 38050977 |
| قاعدة البيانات: | MEDLINE |
| تدمد: | 0893-9675 |
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| DOI: | 10.1615/CritRevOncog.2023048723 |