线粒体
生物标志物
癌症
化学
癌症检测
癌细胞
细胞器
计算生物学
生物标志物发现
癌症生物标志物
癌症治疗
鉴定(生物学)
荧光
纳米技术
癌症研究
生物化学
生物
医学
蛋白质组学
内科学
植物
物理
材料科学
量子力学
基因
作者
Xue Yu,Yunong Huang,Yunqi Tao,Li Fan,Yuewei Zhang
标识
DOI:10.1016/j.aca.2023.342060
摘要
Cancer represents a global threat to human health, and effective strategies for improved cancer early diagnosis and treatment are urgently needed. The detection of tumor biomarkers has been one of the important auxiliary means for tumor screening and diagnosis. Mitochondria are crucial subcellular organelles that produce most chemical energy used by cells, control metabolic processes, and maintain cell function. Evidence suggests the close involvement of mitochondria with cancer development. As a consequence, the identification of cancer-associated biomarker expression levels in mitochondria holds significant importance in the diagnosis of early-stage diseases and the monitoring of therapy efficacy. Small-molecule fluorescent probes are effective for the identification and visualization of bioactive entities within biological systems, owing to their heightened sensitivity, expeditious non-invasive analysis and real-time detection capacities. The design principles and sensing mechanisms of mitochondrial targeted fluorescent probes are summarized in this review. Additionally, the biomedical applications of these probes for detecting cancer-associated biomarkers are highlighted. The limitations and challenges of fluorescent probes in vivo are also considered and some future perspectives are provided. This review is expected to provide valuable insights for the future development of novel fluorescent probes for clinical imaging, thereby contributing to the advancement of cancer diagnosis and treatment.
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