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Updated: Jan 10, 2026

Dual-color Correlative Light and Electron Microscopy for the Visualization of Interactions between Mitochondria and Lysosomes
Published on: September 27, 2024
Mitochondria-located circRCP regulates redox homeostasis via stabilizing LRPPRC/SLIRP complex to promote bladder
Zhao-Hui Zhou1, Jun-Hua Wen2, Yuan-Zhe Zhang3
1State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China; Department of Urology, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Abstract:
The function of circular RNAs (circRNAs) located within the mitochondria in the pathogenesis of urothelial carcinoma of the bladder (UCB) remains largely unexplored. This study identified a mitochondria-located circRNA named circRCP from the nuclear genome of UCB cells. It is frequently upregulated in UCB and serves as an independent prognostic factor. This study further illustrates that circRCP enhances UCB tumorigenesis by regulating intracellular redox homeostasis. The knockdown of circRCP heightens mitochondrial oxidative stress, which leads to ROS generation, consequently triggering UCB cell apoptosis. Mechanistically, by forming a circRCP/LRPPRC/SLIRP RNA-protein ternary complex, circRCP enhances the LRPPRC/SLIRP stability and protects LRPPRC from ubiquitination and proteasomal degradation. Clinically, UCBs exhibiting high circRCP and LRPPRC expression had the worst outcomes. Taken together, we have identified a mitochondria-located circRNA that protects UCB cells from oxidative stress, highlighting its potential role in UCB pathogenesis and warranting further investigation into its therapeutic applicability.
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