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靶向肿瘤干细胞的 NK 细胞治疗:新瓶装旧酒

英文原题:Natural killer cell therapy targeting cancer stem cells: Old wine in a new bottle.

查看英文原题

Natural killer cell therapy targeting cancer stem cells: Old wine in a new bottle.

PubMed 2023/07/26(内容时间) Cancer Lett Q1 · IF 11.8(JCR 2025)

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中文摘要

一小部分具有干细胞样特性的癌细胞被称为肿瘤干细胞(CSCs)。它们可用于识别恶性肿瘤表型和预后不良的患者。靶向这些细胞已被证明可提高癌症治疗的有效性。由于CSCs的特性,它们对放疗和化疗等传统治疗方法具有耐药性。因此,需要更有效的抗CSC疗法。免疫疗法,包括自然杀伤(NK)细胞和T细胞疗法,已显示出清除CSCs的能力。在识别低水平主要组织相容性复合体(MHC)I类表达方面,NK细胞相比T细胞表现出更优越的抗CSC能力。然而,在NK细胞治疗过程中也会发生CSC逃逸。确定CSC特异性免疫逃逸机制并寻找优化NK细胞功能的潜在解决方案非常重要。因此,本综述讨论了可提高NK细胞疗法治疗CSCs效率的有前景的策略,旨在为未来研究提供参考。

展开英文摘要原文

A small proportion of cancer cells that have stem cell-like properties are known as cancer stem cells (CSCs). They can be used to identify malignant tumor phenotypes and patients with poor prognosis. Targeting these cells has been shown to improve the effectiveness of cancer therapies. Owing to the nature of CSCs, they are resistant to conventional treatment methods such as radio- and chemotherapy.

Therefore, more effective anti-CSC therapies are required. Immunotherapy, including natural killer (NK) and T cell therapy, has demonstrated the ability to eliminate CSCs. NK cells have demonstrated superior anti-CSC capabilities compared to T cells in recognizing low levels of major histocompatibility complex (MHC) class I expression.

However, CSC escape also occurs during NK cell therapy. It is important to determine CSC-specific immune evasion mechanisms and find out potential solutions to optimize NK cell function.

Therefore, this review discusses promising strategies that can improve the efficiency of NK cell therapy in treating CSCs, and aims to provide a reference for future research.

论文信息

作者
Guo F、Zhang Y、Bai L、Cui J
第一作者单位
Cancer Center, The First Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.China
通讯作者单位
Cancer Center, The First Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China. Electronic address: cuijw@jlu.edu.cn.China
文献类型
综述
期刊
Cancer letters2023 Aug 28
原文标识
PubMed 37499742 · DOI 10.1016/j.canlet.2023.216328