自噬
癌症
转移
前列腺癌
癌症研究
机制(生物学)
医学
线粒体融合
癌细胞
线粒体
程序性细胞死亡
癌变
细胞凋亡
生物
生物信息学
细胞生物学
线粒体DNA
内科学
基因
认识论
哲学
生物化学
作者
T. Rana,Akhilesh Prajapati
标识
DOI:10.5306/wjco.v16.i7.107788
摘要
New approaches in cancer treatment are increasingly emphasizing innovative biological processes such as ferroptosis, autophagy, and mitochondrial dynamics. Ferroptosis, characterized by iron-dependent lipid peroxidation, has emerged as a promising strategy for targeting aggressive and metastatic cancers including those of the lung, breast, prostate, pancreas, and colorectal regions. Autophagy, a cellular degradation mechanism, plays a dual role in cancer—it can inhibit tumor development by clearing damaged cellular components or, paradoxically, support tumor growth under stressful conditions. Mitochondrial dynamics, encompassing the continuous processes of fission and fusion, are often disrupted in various types of human cancers, leading to altered metabolism, therapy resistance, and metastasis. These disruptions make them favorable targets for innovative treatments. This review highlights ferroptosis as a novel form of cell death, focusing on its biological pathways and connections with mitochondrial dysfunction and autophagy. Understanding the interplay among these three mechanisms in the complex biology of cancer could provide a more comprehensive and effective approach to cancer therapy.
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