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Published on: May 12, 2020
The mitochondrial nexus: Targeting metabolic vulnerabilities, oxidative stress, and immunomodulation to induce cancer
1Department of Physiology, Medical School, Jeonbuk National University, Jeonju 54896, Republic of Korea.
Abstract:
Mitochondria, far from being mere cellular powerhouses, act as central command hubs dictating cell fate by integrating metabolic cues with life-or-death decisions. In cancer, these organelles undergo profound functional and structural reprogramming to support relentless proliferation, survival, and adaptation to stress. This metabolic plasticity, however, creates unique vulnerabilities exploitable for therapeutic gain. This comprehensive review synthesizes recent insights into the multifaceted roles of mitochondria in cancer, focusing on how inhibiting their core functions can trigger diverse cell death pathways and modulate the tumor microenvironment. This paper delves into the central role of mitochondria in orchestrating various forms of regulated cell death (RCD), including apoptosis, ferroptosis, necroptosis, and the newly defined cuproptosis. A primary focus is placed on the dual nature of mitochondrial reactive oxygen species (ROS), which can promote tumorigenesis but can also be pharmacologically elevated to catastrophic levels, triggering oxidative stress-induced demise. This review systematically categorizes and discusses a burgeoning pharmacopeia of mitochondrial inhibitors-targeting the electron transport chain (ETC), metabolic enzymes like glutaminase, protein homeostasis, and ion channels-and analyzes their mechanisms of action, preclinical evidence, and clinical translation status. Furthermore, this paper examines how these agents can overcome chemoresistance and synergize with existing treatments, including the exciting interface with immunotherapy, where mitochondrial fitness is paramount for robust anti-tumor T-cell responses and the induction of immunogenic cell death (ICD). By dissecting the complex interplay between mitochondrial inhibition, metabolic disruption, oxidative stress, and cell death, this review highlights the immense promise of mitochondria-targeted therapies and charts the course for future innovations in oncology.
Insights
Mitochondria are key in cancer, driving proliferation and survival. Targeting mitochondrial functions offers new therapeutic strategies by inducing cell death and enhancing anti-cancer immunity.
Area of Science:
- Mitochondrial biology
- Cancer cell metabolism
- Oncology therapeutics
Background:
- Mitochondria regulate cell fate and adapt to cancer's metabolic demands.
- Cancer cells reprogram mitochondria for proliferation, survival, and stress adaptation.
- This metabolic plasticity presents therapeutic vulnerabilities.
Purpose of the Study:
- To review the roles of mitochondria in cancer.
- To explore how inhibiting mitochondrial functions can induce cell death and modulate the tumor microenvironment.
- To discuss mitochondria-targeted therapies and their clinical potential.
Main Methods:
- Comprehensive review of recent literature on mitochondria in cancer.
- Systematic categorization of mitochondrial inhibitors targeting electron transport chain, metabolic enzymes, protein homeostasis, and ion channels.
- Analysis of mechanisms of action, preclinical data, and clinical translation.
Main Results:
- Mitochondria orchestrate various forms of regulated cell death (RCD), including apoptosis, ferroptosis, necroptosis, and cuproptosis.
- Mitochondrial reactive oxygen species (ROS) have a dual role in tumorigenesis and cell death induction.
- Mitochondrial inhibitors show promise in overcoming chemoresistance and synergizing with immunotherapy.
Conclusions:
- Targeting mitochondrial functions is a promising therapeutic strategy in oncology.
- Mitochondrial inhibition can trigger diverse cell death pathways and enhance anti-tumor immunity.
- Future research should focus on developing and translating novel mitochondria-targeted therapies.
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