Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10771709 | Biochemical and Biophysical Research Communications | 2005 | 6 Pages |
Abstract
The novel cyclic dinucleotide, 3â²,5â²-cyclic diguanylic acid, cGpGp (c-di-GMP), is a naturally occurring small molecule that regulates important signaling mechanisms in prokaryotes. Recently, we showed that c-di-GMP has “drug-like” properties and that c-di-GMP treatment might be a useful antimicrobial approach to attenuate the virulence and pathogenesis of Staphylococcus aureus and prevent or treat infection. In the present communication, we report that c-di-GMP (⩽50 μM) has striking properties regarding inhibition of cancer cell proliferation in vitro. c-di-GMP inhibits both basal and growth factor (acetylcholine and epidermal growth factor)-induced cell proliferation of human colon cancer (H508) cells. Toxicity studies revealed that exposure of normal rat kidney cells and human neuroblastoma cells to c-di-GMP at biologically relevant doses showed no lethal cytotoxicity. Cyclic dinucleotides, such as c-di-GMP, represent an attractive and novel “drug-platform technology” that can be used not only to develop new antimicrobial agents, but also to develop novel therapeutic agents to prevent or treat cancer.
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Authors
David K.R. Karaolis, Kunrong Cheng, Michael Lipsky, Ahmed Elnabawi, Jennifer Catalano, Mamoru Hyodo, Yoshihiro Hayakawa, Jean-Pierre Raufman,