Expanded Alternatives of CRISPR-Cas9 Applications in Immunotherapy of Colorectal Cancer

被引:1
作者
Arroyo-Olarte, Ruben [1 ,2 ]
Mejia-Munoz, Aranza [1 ,2 ]
Leon-Cabrera, Sonia [1 ,2 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Estudios Super Iztacala, Unidad Biomed, Ave Los Barrios 1, Tlalnepantla 54090, Edo De Mexico, Mexico
[2] Univ Nacl Autonoma Mexico, Fac Estudios Super Iztacala, Carrera Med Cirujano, Tlalnepantla 54090, Edo De Mexico, Mexico
关键词
CAR-T-CELLS; PROGNOSTIC-SIGNIFICANCE; RECEPTOR EXPRESSION; ANTITUMOR-ACTIVITY; IN-VITRO; CARCINOMA; CHALLENGES; MUTATIONS; HALLMARKS; EFFICACY;
D O I
10.1007/s40291-023-00680-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Immunotherapy for colorectal cancer (CRC) is limited to patients with advanced disease who have already undergone first-line chemotherapy and whose tumors exhibit microsatellite instability. Novel technical strategies are required to enhance therapeutic options and achieve a more robust immunological response. Therefore, exploring gene analysis and manipulation at the molecular level can further accelerate the development of advanced technologies to address these challenges. The emergence of advanced genome editing technology, particularly of clustered, regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein (Cas) 9, holds promise in expanding the boundaries of cancer immunotherapy. In this manuscript, we provide a comprehensive review of the applications and perspectives of CRISPR technology in improving the design, generation, and efficiency of current immunotherapies, focusing on solid tumors such as colorectal cancer, where these approaches have not been as successful as in hematological conditions.
引用
收藏
页码:69 / 86
页数:18
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