In normal cells, intrinsic mechanisms exist to repair radiation-induced damage through activation of intracellular signaling pathways. Intracellular signaling is used by the cell to control information flow and subsequent growth, life and cell division. The repair signaling pathways are normal and present in all cells. They continually operate at low levels in an oversight mode to monitor and repair low levels of damage to the DNA. The effectiveness of these repair mechanisms can vary with genetic background and the intensity of exposure and are often insufficient to deal with larger doses of radiation. Inositol signaling molecules (ISMs) are key components of intracellular signaling and figure prominently in the regulation of radiation repair mechanisms. ISMs regulate activity of proteins in radiation response and DNA repair pathways by facilitating double stranded break (DSB) repair and non-homologous end joining.



