1. Triggering of Apoptosis in Osteosarcoma 143B Cell Line by Carbon Quantum Dots via the Mitochondrial Apoptotic Signal Pathway
- Author
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Yimin Guo, Zhichao Meng, Xiang Li, Hao Wu, Xin Yang, Yingcong Fan, Talatibaike Maimaitijuma, Jiazhen Zhang, Yunpeng Cui, Yongping Cao, Liping Pan, Yahong Wang, Rui Wang, Tao Zhang, Yang Jiao, and Heng Liu
- Subjects
0301 basic medicine ,Male ,Article Subject ,Mice, Nude ,Antineoplastic Agents ,Apoptosis ,02 engineering and technology ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,chemistry.chemical_compound ,Annexin ,In vivo ,Cell Line, Tumor ,Quantum Dots ,Animals ,Humans ,Propidium iodide ,Fluorescein isothiocyanate ,Cytotoxicity ,Cell Proliferation ,Membrane Potential, Mitochondrial ,Mice, Inbred BALB C ,Osteosarcoma ,General Immunology and Microbiology ,General Medicine ,021001 nanoscience & nanotechnology ,Molecular biology ,Carbon ,Mitochondria ,030104 developmental biology ,chemistry ,Medicine ,Apoptotic signaling pathway ,0210 nano-technology ,Reactive Oxygen Species ,Intracellular ,Research Article ,Signal Transduction - Abstract
Objectives. Carbon-based nanomaterials have gained attention in the field of biomedicine in recent years, especially for the treatment of complicated diseases such as cancer. Here, we report a novel carbon-based nanomaterial, named carbon quantum dots (CQDs), which has potential for cancer therapy. We performed a systematic study on the effects of CQDs on the osteosarcoma 143B cell line in vitro and in vivo. Methods. Cell counting assay, the neutral red assay, lactic dehydrogenase assay, and fluorescein isothiocyanate (FITC) Annexin V/Propidium iodide (PI) were used to detect the cytotoxicity and apoptosis of CQDs on the 143B cell line. Intracellular reactive oxygen species (ROS) were detected by the oxidation-sensitive fluorescent probe 2′,7′-dichlorofluorescein diacetate. The JC-10 assay was used to detect the mitochondrial membrane potential (MMP) of 143B cells incubated with CQDs. The effects of CQDs on the 143B cell line were evaluated by Western blot and immunofluorescence analysis of apoptosis-related proteins Bax, Bcl-2, cytochrome-C, caspase-3, cleaved-caspase-3, PARP1, and cleaved-PARP1. Male tumor-bearing BALB/c nude mice were used to investigate the antitumor effects of CQDs, and the biosafety of CQDs in vivo was tested in male BALB/c mice by measuring weight changes, hematology tests, and histological analyses of major organs. Results. CQDs exhibited a high cytotoxicity and induced apoptosis toward the 143B cell line. CQDs can also significantly increase the intracellular level of ROS and lower the mitochondrial membrane potential levels of 143B cells. CQDs increase apoptotic protein expression to induce apoptosis of 143B cells by triggering the mitochondrial apoptotic signaling pathway. The tumor volume in the CQD-treated mice was smaller than that in the control group, the tumor volume inhibition rate was 38.9%, and the inhibitory rate by tumor weight was 30.1%. All biosafety test indexes were within reference ranges, and neither necrosis nor inflammation was observed in major organs. Conclusions. CQDs induced cytotoxicity in the 143B cell line through the mitochondrial apoptotic signaling pathway. CQDs not only showed an antitumor effect but also high biocompatibility in vivo. As a new carbon-based nanomaterial, CQDs usage is a promising method for novel cancer treatments.
- Published
- 2020