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化学耐药性简述;以肿瘤干细胞为靶点的治疗策略。

A Brief Review on Chemoresistance; Targeting Cancer Stem Cells as an Alternative Approach.

机构信息

Department of Health Sciences, University of Jaén, Campus de las Lagunillas, 23071 Jaen, Spain.

Excellence Research Unit "Modeling Nature" (MNat), University of Granada, 18016 Granada, Spain.

出版信息

Int J Mol Sci. 2023 Feb 24;24(5):4487. doi: 10.3390/ijms24054487.

Abstract

The acquisition of resistance to traditional chemotherapy and the chemoresistant metastatic relapse of minimal residual disease both play a key role in the treatment failure and poor prognosis of cancer. Understanding how cancer cells overcome chemotherapy-induced cell death is critical to improve patient survival rate. Here, we briefly describe the technical approach directed at obtaining chemoresistant cell lines and we will focus on the main defense mechanisms against common chemotherapy triggers by tumor cells. Such as, the alteration of drug influx/efflux, the enhancement of drug metabolic neutralization, the improvement of DNA-repair mechanisms, the inhibition of apoptosis-related cell death, and the role of and reactive oxygen species (ROS) levels in chemoresistance. Furthermore, we will focus on cancer stem cells (CSCs), the cell population that subsists after chemotherapy, increasing drug resistance by different processes such as epithelial-mesenchymal transition (EMT), an enhanced DNA repair machinery, and the capacity to avoid apoptosis mediated by BCL2 family proteins, such as BCL-XL, and the flexibility of their metabolism. Finally, we will review the latest approaches aimed at decreasing CSCs. Nevertheless, the development of long-term therapies to manage and control CSCs populations within the tumors is still necessary.

摘要

对传统化疗的耐药性的获得以及微小残留病的化疗耐药性转移复发,均在癌症治疗失败和预后不良中发挥关键作用。了解癌细胞如何克服化疗诱导的细胞死亡,对于提高患者生存率至关重要。在这里,我们简要描述了获得耐药细胞系的技术方法,并将重点介绍肿瘤细胞对抗常见化疗触发因素的主要防御机制。例如,药物摄取/流出的改变、药物代谢中和作用的增强、DNA 修复机制的改善、凋亡相关细胞死亡的抑制,以及活性氧 (ROS) 水平在化疗耐药性中的作用。此外,我们将重点关注癌症干细胞 (CSC),即化疗后存活的细胞群体,通过不同的过程增加药物耐药性,如上皮-间充质转化 (EMT)、增强的 DNA 修复机制以及逃避 BCL2 家族蛋白(如 BCL-XL)介导的细胞凋亡的能力,以及其代谢的灵活性。最后,我们将回顾旨在降低 CSCs 的最新方法。然而,仍然需要开发长期的治疗方法来管理和控制肿瘤内的 CSCs 群体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa27/10003376/96b26a84ea3a/ijms-24-04487-g001.jpg

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