| Literature DB >> 30753755 |
Xinqi Zhou1, Yuan Fang1, Lauren Lesiak1, Cliff I Stains1,2,3.
Abstract
Chemotherapeutic agents generally suffer from off-target cytotoxicity in noncancerous cell types, leading to undesired side effects. As a result, significant effort has been put into identifying compounds that are selective for cancerous over noncancerous cell types. Our laboratory has recently developed a series of near-infrared (NIR) fluorophores containing a phosphinate functionality at the bridging position of a xanthene scaffold, termed Nebraska Red (NR) fluorophores. Herein, we report the selective cytotoxicity of one NR derivative, NR744 , against HeLa (cervical cancer) cells versus NIH-3T3 (noncancerous fibroblast) cells. Mechanistic studies based on the NIR fluorescence signal of NR744 showed distinct subcellular localization in HeLa (mitochondrial) versus NIH-3T3 (lysosomal) that resulted from the elevated mitochondrial potential in HeLa cells. This study provides a new, NIR scaffold for the further development of reagents for targeted cancer therapy.Entities:
Keywords: apoptosis; cancer; cytotoxicity; fluorescence probes; phosphinate
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Year: 2019 PMID: 30753755 PMCID: PMC6663559 DOI: 10.1002/cbic.201800811
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164