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CRISPR/Cas9技术为转移性前列腺癌提供治疗前景。

CRISPR/Cas9 Technology Providing the Therapeutic Landscape of Metastatic Prostate Cancer.

作者信息

Park Jieun, Kim Jaehong

机构信息

Department of Neurology, College of Medicine, Dongguk University, Ilsan, Goyang 10326, Republic of Korea.

Department of Biochemistry, College of Medicine, Gachon University, Incheon 21999, Republic of Korea.

出版信息

Pharmaceuticals (Basel). 2024 Nov 26;17(12):1589. doi: 10.3390/ph17121589.

Abstract

Prostate cancer (PCa) is the most prevalent malignancy and the second leading cause of cancer-related death in men. Although current therapies can effectively manage the primary tumor, most patients with late-stage disease manifest with metastasis in different organs. From surgery to treatment intensification (TI), several combinations of therapies are administered to improve the prognosis of patients with metastatic PCa. Due to the high frequency of the mutation during the metastatic phase, the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated nuclease 9 (Cas9) genetic engineering tool can accelerate the effects of TI by enhancing targeted gene therapy or immunotherapy. This review describes the genetic background of metastatic PCa and how CRISPR/Cas9 technology can contribute to the field of PCa treatment development. It also discusses the current limitations of conventional PCa therapy and the potential of CRISPR-based PCa therapy.

摘要

前列腺癌(PCa)是男性中最常见的恶性肿瘤,也是癌症相关死亡的第二大主要原因。尽管目前的治疗方法可以有效控制原发性肿瘤,但大多数晚期疾病患者会出现不同器官的转移。从手术到强化治疗(TI),多种治疗组合被用于改善转移性PCa患者的预后。由于在转移阶段突变频率较高,成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关核酸酶9(Cas9)基因工程工具可通过增强靶向基因治疗或免疫治疗来加速强化治疗的效果。本综述描述了转移性PCa的遗传背景,以及CRISPR/Cas9技术如何为PCa治疗发展领域做出贡献。它还讨论了传统PCa治疗的当前局限性以及基于CRISPR的PCa治疗的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d5b/11676443/285d1fd194fb/pharmaceuticals-17-01589-g001.jpg

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