Published April 1, 2005 | Version v1
Journal article

3',5'-Cyclic diguanylic acid (c-di-GMP) inhibits basal and growth factor-stimulated human colon cancer cell proliferation

  • 1. Department of Epidemiology and Preventive Medicine, University of Maryland School of Medicine, Baltimore, MD 21201 (United States)
  • 2. Department of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201 (United States)
  • 3. Department of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201 (United States)
  • 4. Department of Pharmacology and Experimental Therapeutics, University of Maryland School of Medicine, Baltimore, MD 21201 (United States)
  • 5. Graduate School of Information Science/Human Informatics and CREST/JST, Nagoya University, Nagoya 464-8601 (Japan)

Description

The novel cyclic dinucleotide, 3',5'-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

Additional details

Identifiers

DOI
10.1016/j.bbrc.2005.01.093;
PII
S0006-291X(05)00110-5;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
329
Journal Issue
1
Journal Page Range
p. 40-45
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.