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自然杀伤细胞在癌症干细胞的黑暗世界中增多。

NK cell upraise in the dark world of cancer stem cells.

作者信息

Shokouhifar Alireza, Firouzi Javad, Nouri Masoumeh, Sarab Gholamreza Anani, Ebrahimi Marzieh

机构信息

Department of Molecular Medicine, Genomic Research Center, Birjand University of Medical Sciences, Birjand, Iran.

Cellular & Molecular Research Center, Birjand University of Medical Sciences, Birjand, Iran.

出版信息

Cancer Cell Int. 2021 Dec 19;21(1):682. doi: 10.1186/s12935-021-02400-1.

Abstract

One of the obstacles in treating different cancers, especially solid tumors, is cancer stem cells (CSCs) with their ability in resistance to chemo/radio therapy. The efforts for finding advanced treatments to overcome these cells have led to the emergence of advanced immune cell-based therapy (AICBT). Today, NK cells have become the center of attention since they have been proved to show an appropriate cytotoxicity against different cancer types as well as the capability of detecting and killing CSCs. Attempts for reaching an off-the-shelf source of NK cells have been made and resulted in the emergence of chimeric antigen receptor natural killer cells (CAR-NK cells). The CAR technology has then been used for generating more cytotoxic and efficient NK cells, which has increased the hope for cancer treatment. Since utilizing this advanced technology to target CSCs have been published in few studies, the present study has focused on discussing the characteristics of CSCs, which are detected and targeted by NK cells, the advantages and restrictions of using CAR-NK cells in CSCs treatment and the probable challenges in this process.

摘要

治疗不同癌症(尤其是实体瘤)的障碍之一是癌症干细胞(CSCs),它们具有对化疗/放疗的抗性。寻找先进治疗方法以克服这些细胞的努力导致了先进的基于免疫细胞的疗法(AICBT)的出现。如今,NK细胞已成为关注的焦点,因为它们已被证明对不同类型的癌症表现出适当的细胞毒性,以及检测和杀死癌症干细胞的能力。人们已尝试获得现成的NK细胞来源,并由此产生了嵌合抗原受体自然杀伤细胞(CAR-NK细胞)。然后,CAR技术被用于产生更具细胞毒性和高效的NK细胞,这增加了癌症治疗的希望。由于利用这种先进技术靶向癌症干细胞的研究较少,本研究专注于讨论被NK细胞检测和靶向的癌症干细胞的特征、在癌症干细胞治疗中使用CAR-NK细胞的优势和限制以及这一过程中可能面临的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df4c/8684645/7b35d1929546/12935_2021_2400_Fig1_HTML.jpg

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