Polyphosphate Affects on Breast Cancer Cell Survival

摘要

The research supported by the Department of Defense Breast Cancer Research Program (BCRP) studies whether the polyphosphate survival function is conserved between prokaryotes and eukaryotes and specifically whether polyphosphates are involved in the increased survival of breast cancer cells. While in the process of developing modified MCF-7 breast cancer cells, an exciting opportunity arose to investigate polyphosphates and their effect on DNA damage response. It is well documented that DNA damaging agents can cause genomic instability and lead to various forms of cancer including breast cancer. Without proper cell cycle checkpoints that trigger repair of the damage or induction of apoptosis, genetic mutations can be propagated, possibly initiating tumorigenesis. Functional analysis of DNA damage response, cell cycle checkpoints which involve BRCA1, genome integrity, and tumor evolution will build the knowledge of the mechanisms involved in breast cancer The principle investigator ceased this opportunity to study polyphosphates and DNA damage response with respect to cell survival and DNA repair mutagenesis and the DNA damage response (SOS response) which follows extensive DNA damage. It has been discovered that: Loss of ability to synthesize polyphosphates compromises cellular survival after DNA damage; This effect is not exclusive to a specific DNA damaging agent; This loss of survival is not directly linked to the general stress response pathway; This compromised survival is independent of cellular growth phase or growth rate; Polyphosphates levels increase transiently after DNA damage; Elevated polyphosphate levels are not dependent on the SOS genes recA, dinB, or umuDC; The ability to synthesize polyphosphates influences Pol IV activity.