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CRISPR技术在癌症治疗领域的潜在变革

The Potential Revolution of Cancer Treatment with CRISPR Technology.

作者信息

Stefanoudakis Dimitrios, Kathuria-Prakash Nikhita, Sun Alexander W, Abel Melissa, Drolen Claire E, Ashbaugh Camille, Zhang Shiliang, Hui Gavin, Tabatabaei Yeganeh A, Zektser Yuliya, Lopez Lidia P, Pantuck Allan, Drakaki Alexandra

机构信息

School of Medicine, National & Kapodistrian University of Athens, 15772 Athens, Greece.

Division of Hematology and Oncology, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.

出版信息

Cancers (Basel). 2023 Mar 17;15(6):1813. doi: 10.3390/cancers15061813.

Abstract

Immuno-oncology (IO) and targeted therapies, such as small molecule inhibitors, have changed the landscape of cancer treatment and prognosis; however, durable responses have been difficult to achieve due to tumor heterogeneity, development of drug resistance, and adverse effects that limit dosing and prolonged drug use. To improve upon the current medicinal armamentarium, there is an urgent need for new ways to understand, reverse, and treat carcinogenesis. Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein (Cas) 9 is a powerful and efficient tool for genome editing that has shown significant promise for developing new therapeutics. While CRISPR/Cas9 has been successfully used for pre-clinical cancer research, its use in the clinical setting is still in an early stage of development. The purpose of this review is to describe the CRISPR technology and to provide an overview of its current applications and future potential as cancer therapies.

摘要

免疫肿瘤学(IO)和靶向疗法,如小分子抑制剂,已经改变了癌症治疗和预后的格局;然而,由于肿瘤异质性、耐药性的产生以及限制剂量和延长药物使用的不良反应,难以实现持久的反应。为了改进当前的药物库,迫切需要新的方法来理解、逆转和治疗致癌作用。成簇规律间隔短回文重复序列(CRISPR)-CRISPR相关蛋白(Cas)9是一种强大而高效的基因组编辑工具,在开发新疗法方面显示出巨大的潜力。虽然CRISPR/Cas9已成功用于临床前癌症研究,但其在临床环境中的应用仍处于早期发展阶段。本综述的目的是描述CRISPR技术,并概述其作为癌症疗法的当前应用和未来潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9628/10046289/75a2ae40dea8/cancers-15-01813-g001.jpg

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