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靶向乳腺癌干细胞。

Targeting Breast Cancer Stem Cells.

机构信息

Fudan University Shanghai Cancer Center & Institutes of Biomedical Sciences; State Key Laboratory of Genetic Engineering; Cancer Institutes; Key Laboratory of Breast Cancer in Shanghai; The Shanghai paracrine Key Laboratory of Medical Epigenetics; Shanghai Key Laboratory of Radiation Oncology; The International Co-laboratory of Medical Epigenetics and Metabolism, Ministry of Science and Technology; Shanghai Medical College; Fudan University, Shanghai 200032, China.

Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences and Yunnan Province, Kunming Institute of Zoology, Kunming 650201, China.

出版信息

Int J Biol Sci. 2023 Jan 1;19(2):552-570. doi: 10.7150/ijbs.76187. eCollection 2023.

Abstract

The potential roles of breast cancer stem cells (BCSCs) in tumor initiation and recurrence have been recognized for many decades. Due to their strong capacity for self-renewal and differentiation, BCSCs are the major reasons for poor clinical outcomes and low therapeutic response. Several hypotheses on the origin of cancer stem cells have been proposed, including critical gene mutations in stem cells, dedifferentiation of somatic cells, and cell plasticity remodeling by epithelial-mesenchymal transition (EMT) and the tumor microenvironment. Moreover, the tumor microenvironment, including cellular components and cytokines, modulates the self-renewal and therapeutic resistance of BCSCs. Small molecules, antibodies, and chimeric antigen receptor (CAR)-T cells targeting BCSCs have been developed, and their applications in combination with conventional therapies are undergoing clinical trials. In this review, we focus on the features of BCSCs, emphasize the major factors and tumor environment that regulate the stemness of BCSCs, and discuss potential BCSC-targeting therapies.

摘要

几十年来,人们已经认识到乳腺癌干细胞(BCSCs)在肿瘤发生和复发中的潜在作用。由于其强大的自我更新和分化能力,BCSCs 是导致临床预后不良和治疗反应率低的主要原因。目前已经提出了几种关于癌症干细胞起源的假说,包括干细胞中的关键基因突变、体细胞去分化以及上皮-间充质转化(EMT)和肿瘤微环境引起的细胞可塑性重塑。此外,肿瘤微环境包括细胞成分和细胞因子,调节 BCSC 的自我更新和治疗抵抗能力。已经开发了针对 BCSC 的小分子、抗体和嵌合抗原受体(CAR)-T 细胞,并且正在临床试验中研究它们与常规疗法联合应用。在这篇综述中,我们重点关注 BCSC 的特征,强调调节 BCSC 干性的主要因素和肿瘤微环境,并讨论潜在的 BCSC 靶向治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a7f/9830502/ca8f5ddfddaa/ijbsv19p0552g001.jpg

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