Rozenberg Julian Markovich, Kamynina Margarita, Sorokin Maksim, Zolotovskaia Marianna, Koroleva Elena, Kremenchutckaya Kristina, Gudkov Alexander, Buzdin Anton, Borisov Nicolas
Moscow Institute of Physics and Technology, National Research University, 141700 Moscow, Russia.
Group of Experimental Biotherapy and Diagnostic, Institute for Regenerative Medicine, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Biomedicines. 2022 May 5;10(5):1072. doi: 10.3390/biomedicines10051072.
Metal ion homeostasis is fundamental for life. Specifically, transition metals iron, manganese and zinc play a pivotal role in mitochondrial metabolism and energy generation, anti-oxidation defense, transcriptional regulation and the immune response. The misregulation of expression or mutations in ion carriers and the corresponding changes in Mn and Zn levels suggest that these ions play a pivotal role in cancer progression. Moreover, coordinated changes in Mn and Zn ion carriers have been detected, suggesting that particular mechanisms influenced by both ions might be required for the growth of cancer cells, metastasis and immune evasion. Here, we present a review of zinc and manganese pathophysiology suggesting that these ions might cooperatively regulate cancerogenesis. Zn and Mn effects converge on mitochondria-induced apoptosis, transcriptional regulation and the cGAS-STING signaling pathway, mediating the immune response. Both Zn and Mn influence cancer progression and impact treatment efficacy in animal models and clinical trials. We predict that novel strategies targeting the regulation of both Zn and Mn in cancer will complement current therapeutic strategies.
金属离子稳态是生命的基础。具体而言,过渡金属铁、锰和锌在线粒体代谢与能量生成、抗氧化防御、转录调控及免疫反应中发挥着关键作用。离子载体表达的失调或突变以及锰和锌水平的相应变化表明,这些离子在癌症进展中起关键作用。此外,已检测到锰和锌离子载体的协同变化,这表明癌细胞生长、转移和免疫逃逸可能需要受这两种离子影响的特定机制。在此,我们综述锌和锰的病理生理学,表明这些离子可能协同调节肿瘤发生。锌和锰的作用集中在线粒体诱导的细胞凋亡、转录调控和cGAS-STING信号通路,介导免疫反应。在动物模型和临床试验中,锌和锰均影响癌症进展并影响治疗效果。我们预测,针对癌症中锌和锰调节的新策略将补充当前的治疗策略。