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癌症干细胞靶向的生物成像和化学治疗视角。

Cancer stem cell-targeted bio-imaging and chemotherapeutic perspective.

机构信息

Department of Biological Sciences, Hyupsung University, Hwasung-si, 18330, Korea.

出版信息

Chem Soc Rev. 2020 Nov 21;49(22):7856-7878. doi: 10.1039/d0cs00379d. Epub 2020 Jul 7.

Abstract

Cancer stem cells (CSCs), also called tumor-initiating cells (TICs), have been studied intensively due to their rapid proliferation, migration, and role in the recurrence of cancer. In general, CSC marker-positive cells [CD133, CD44, CD166, aldehyde dehydrogenase (ALDH), and epithelial cell adhesion molecule (EpCAM)] exhibit a 100-fold increased capacity to initiate cancer. Within a heterogeneous tumor mass, only approximately 0.05-3% of cells are suspected to be CSCs and able to proliferate under hypoxia. Interestingly, CSCs, cancer cells, and normal stem cells share many cytochemical properties, such as inhibition of the redox system for reactive oxygen species (ROS) production and high expression of drug resistance transporters. However, compared to normal stem cells, CSCs develop unique metabolic flexibility, which involves switching between oxidative phosphorylation (OXPHOS) and glycolysis as their main source of energy. Due to the similarities between CSCs and other cancer cells and normal stem cells, limited chemotherapeutic and bio-imaging reagents specific for CSCs have been developed. In this short review, we address the current knowledge regarding CSCs with a focus on designing chemotherapeutic and bio-imaging reagents that target CSCs.

摘要

癌症干细胞(CSCs),也称为肿瘤起始细胞(TICs),由于其快速增殖、迁移以及在癌症复发中的作用,已受到广泛研究。通常,CSC 标志物阳性细胞[CD133、CD44、CD166、乙醛脱氢酶(ALDH)和上皮细胞黏附分子(EpCAM)]表现出 100 倍的起始癌症能力。在异质肿瘤块中,只有约 0.05-3%的细胞被怀疑是 CSCs,并且能够在缺氧下增殖。有趣的是,CSCs、癌细胞和正常干细胞具有许多细胞化学特性,例如抑制活性氧(ROS)产生的氧化还原系统和高表达药物抗性转运蛋白。然而,与正常干细胞相比,CSCs 具有独特的代谢灵活性,其涉及氧化磷酸化(OXPHOS)和糖酵解之间的切换,作为其主要能量来源。由于 CSCs 与其他癌细胞和正常干细胞之间存在相似性,因此针对 CSCs 开发的有限的化学治疗和生物成像试剂特异性较低。在这篇简短的综述中,我们重点讨论了关于 CSCs 的最新知识,并设计了针对 CSCs 的化学治疗和生物成像试剂。

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