Guo Jie, Yang Wen-Tao, Mai Feng-Yi, Liang Jing-Rong, Luo Jiao, Zhou Ming-Chao, Yu Dong-Dong, Wang Yu-Long, Li Chen-Guang
Department of Rehabilitation Medicine, Shenzhen Second People's Hospital, Shenzhen, China.
Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, National-Regional Key Technology Engineering Laboratory for Medical Ultrasound, School of Biomedical Engineering, Shenzhen University Medical School, Shenzhen, China.
Front Immunol. 2024 Aug 29;15:1450998. doi: 10.3389/fimmu.2024.1450998. eCollection 2024.
Programmed cell death (PCD) is a fundamental biological process for maintaining cellular equilibrium and regulating development, health, and disease across all living organisms. Among the various types of PCD, apoptosis plays a pivotal role in numerous diseases, notably cancer. Cancer cells frequently develop mechanisms to evade apoptosis, increasing resistance to standard chemotherapy treatments. This resistance has prompted extensive research into alternative mechanisms of programmed cell death. One such pathway is oncosis, characterized by significant energy consumption, cell swelling, dilation of the endoplasmic reticulum, mitochondrial swelling, and nuclear chromatin aggregation. Recent research suggests that oncosis can impact conditions such as chemotherapeutic cardiotoxicity, myocardial ischemic injury, stroke, and cancer, mediated by specific oncosis-related proteins. In this review, we provide a detailed examination of the morphological and molecular features of oncosis and discuss various natural or small molecule compounds that can induce this type of cell death. Additionally, we summarize the current understanding of the molecular mechanisms underlying oncosis and its role in both normal physiology and pathological conditions. These insights aim to illuminate future research directions and propose innovative strategies for leveraging oncosis as a therapeutic tool against human diseases and cancer resistance.
程序性细胞死亡(PCD)是维持细胞平衡以及调节所有生物体发育、健康和疾病的基本生物学过程。在各种类型的程序性细胞死亡中,凋亡在众多疾病尤其是癌症中起着关键作用。癌细胞常常形成逃避凋亡的机制,从而增强对标准化疗的抗性。这种抗性促使人们对程序性细胞死亡的替代机制展开广泛研究。其中一条途径是胀亡,其特征是大量能量消耗、细胞肿胀、内质网扩张、线粒体肿胀以及核染色质聚集。近期研究表明,胀亡可通过特定的胀亡相关蛋白介导,影响诸如化疗心脏毒性、心肌缺血损伤、中风和癌症等病症。在本综述中,我们详细审视了胀亡的形态学和分子特征,并讨论了能够诱导此类细胞死亡的各种天然或小分子化合物。此外,我们总结了目前对胀亡潜在分子机制及其在正常生理学和病理状况中作用的理解。这些见解旨在阐明未来的研究方向,并提出创新性策略,以利用胀亡作为对抗人类疾病和癌症抗性的治疗工具。