Zhang Ling, Liu Yi, Zhou Rou, He Baoyu, Wang Wenjun, Zhang Bin
School of Nursing, Jining Medical University, Jining, China.
School of Public Health, North China University of Science and Technology, Tangshan, China.
Front Oncol. 2022 Jul 4;12:939588. doi: 10.3389/fonc.2022.939588. eCollection 2022.
Cyclophilin D (CypD) is a peptide-proline cis-trans isomerase (PPIase) distributed in the mitochondrial matrix. CypD regulates the opening of the mitochondrial permeability conversion pore (mPTP) and mitochondrial bioenergetics through PPIase activity or interaction with multiple binding partners in mitochondria. CypD initially attracted attention due to its regulation of mPTP overopening-mediated cell death. However, recent studies on the effects of CypD on tumors have shown conflicting results. Although CypD has been proven to promote the aerobic glycolysis in tumor cells, its regulation of malignant characteristics such as the survival, invasion and drug resistance of tumor cells remains controversial. Here, we elaborate the main biological functions of CypD and its relationships with tumor progression identified in recent years, focusing on the dual role of CypD in tumors.
亲环蛋白D(CypD)是一种分布于线粒体基质中的肽脯氨酸顺反异构酶(PPIase)。CypD通过PPIase活性或与线粒体中多个结合伴侣的相互作用来调节线粒体通透性转换孔(mPTP)的开放和线粒体生物能量学。CypD最初因其对mPTP过度开放介导的细胞死亡的调节作用而受到关注。然而,最近关于CypD对肿瘤影响的研究结果相互矛盾。尽管已证实CypD可促进肿瘤细胞的有氧糖酵解,但其对肿瘤细胞存活、侵袭和耐药等恶性特征的调节作用仍存在争议。在此,我们阐述CypD的主要生物学功能及其与近年来发现的肿瘤进展的关系,重点关注CypD在肿瘤中的双重作用。