Mitochondria in colorectal cancer stem cells - a target in drug resistance.

IF 4.6 Q1 ONCOLOGY
Mateus de Almeida Rainho, Priscyanne Barreto Siqueira, Ísis Salviano Soares de Amorim, Andre Luiz Mencalha, Alessandra Alves Thole
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引用次数: 2

Abstract

Colorectal cancer (CRC) is the third most diagnosed cancer and the second most deadly type of cancer worldwide. In late diagnosis, CRC can resist therapy regimens in which cancer stem cells (CSCs) are intimately related. CSCs are a subpopulation of tumor cells responsible for tumor initiation and maintenance, metastasis, and resistance to conventional treatments. In this scenario, colorectal cancer stem cells (CCSCs) are considered an important key for therapeutic failure and resistance. In its turn, mitochondria is an organelle involved in many mechanisms in cancer, including chemoresistance of cytotoxic drugs due to alterations in mitochondrial metabolism, apoptosis, dynamics, and mitophagy. Therefore, it is crucial to understand the mitochondrial role in CCSCs regarding CRC drug resistance. It has been shown that enhanced anti-apoptotic protein expression, mitophagy rate, and addiction to oxidative phosphorylation are the major strategies developed by CCSCs to avoid drug insults. Thus, new mitochondria-targeted drug approaches must be explored to mitigate CRC chemoresistance via the ablation of CCSCs.

Abstract Image

结直肠癌干细胞中的线粒体-耐药性的靶标。
结直肠癌(CRC)是世界上第三大诊断癌症和第二大致命癌症。在晚期诊断中,结直肠癌可以抵抗与癌症干细胞(CSCs)密切相关的治疗方案。CSCs是肿瘤细胞的一个亚群,负责肿瘤的发生、维持、转移和对常规治疗的抵抗。在这种情况下,结直肠癌干细胞(CCSCs)被认为是治疗失败和耐药性的重要关键。反过来,线粒体作为一种细胞器参与了癌症的许多机制,包括由于线粒体代谢、凋亡、动力学和线粒体自噬的改变而导致的细胞毒性药物的化疗耐药。因此,了解线粒体在CCSCs中对结直肠癌耐药的作用至关重要。研究表明,增强抗凋亡蛋白表达、线粒体自噬率和对氧化磷酸化的依赖性是CCSCs避免药物损伤的主要策略。因此,必须探索新的线粒体靶向药物方法,通过消融CCSCs来减轻结直肠癌的化疗耐药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.60
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