Fluorescent Quinolinium Derivative as Novel Mitochondria Probe and Function Modulator by Targeting Mitochondrial RNA.
Bo-Zheng WangYing-Chen ZhouYu-Wei LinXiu-Cai ChenZe-Yi YuYao-Hao XuJia-Heng TanShuo-Bin ChenShuo-Bin ChenPublished in: Molecules (Basel, Switzerland) (2023)
Mitochondria have a crucial role in regulating energy metabolism and their dysfunction has been linked to tumorigenesis. Cancer diagnosis and intervention have a great interest in the development of new agents that target biomolecules within mitochondria. However, monitoring and modulating mitochondria RNA (mtRNA), an essential component in mitochondria, in cells is challenging due to limited functional research and the absence of targeting agents. In this study, we designed and synthesized a fluorescent quinolinium derivative, QUCO-1 , which actively lit up with mtRNA in both normal and cancer cells in vitro. Additionally, we evaluated the function of QUCO-1 as an mtRNA ligand and found that it effectively induced severe mitochondrial dysfunction and OXPHOS inhibition in RKO colorectal cancer cells. Treatment with QUCO-1 resulted in apoptosis, cell cycle blockage at the G2/M phase, and the effective inhibition of cell proliferation. Our findings suggest that QUCO-1 has great potential as a promising probe and therapeutic agent for mtRNA, with the potential for treating colorectal cancer.
Keyphrases
- cell cycle
- cell death
- cell proliferation
- cell cycle arrest
- living cells
- quantum dots
- endoplasmic reticulum
- reactive oxygen species
- oxidative stress
- induced apoptosis
- randomized controlled trial
- endoplasmic reticulum stress
- fluorescent probe
- signaling pathway
- pi k akt
- cancer therapy
- squamous cell carcinoma
- endothelial cells
- lymph node metastasis
- smoking cessation
- water soluble