Cells harbour genetic material in the form of DNA, which contains all the information required for the cell to function. Every time a cell divides this information has to be precisely copied so that the newly made cell receives a perfect replica in order that it, too, can function properly. The inheritance of damaged DNA, however, must be inhibited. In order to recognise altered DNA and prevent it from getting passed on to daughter cells, cells have developed surveillance mechanisms, or checkpoints. Checkpoints stop cells from dividing; thereby allowing more time for the cell to repair damaged genetic material. In some cases, however, the DNA cannot be efficiently repaired even though the checkpoints have been activated. If DNA damage persists for a very long time the cells may eventually turn the checkpoints off without waiting for the DNA to get repaired. This process, referred to as adaptation, may initially seem advantageous to the cell because it can finally grow again. “However, for the whole organism, adaptation is often dangerous, as the unrepaired DNA may lead to diseases such as cancer,” points out Dr. Luke.
The molecular biologists Julia Klermund and Katharina Bender in the team of Brian Luke have found a way to prevent cells from turning off the checkpoint and therefore increase the time available for repair, while at the same time preventing damaged DNA from getting passed to newly made cells. The researchers discovered that the amount of nutrients in the cellular environment is a major factor influencing this process. When cells with DNA damage are exposed to low levels of nutrients, they do not adapt and instead remain fully arrested with an active checkpoint. The same effect was observed when cells with DNA damage were treated with the drug “rapamycin,” which inhibits metabolic signalling and therefore mimics nutrient starvation. “The cells that are in low nutrient conditions end up being much more viable, likely because they have waited for the damaged DNA to be repaired before starting to divide again,” explains Julia Klermund. “We believe that high nutrients are pushing cells to grow and proliferate even when the cells should not, e.g. with damaged DNA. Low nutrient conditions likely ensure that cells will only ‘risk’ dividing when the DNA has been completely repaired,” adds Dr. Luke.
According to the Heidelberg scientist, research from the U.S.A. has recently demonstrated that nutrient starvation or rapamycin treatment can extend cell lifespan and also improve the efficacy of some types of chemotherapy. Brian Luke believes the study at the ZMBH may add important mechanistic details regarding how these effects are achieved and provides clues for further enhancement. Dr. Luke is a member of the DKFZ-ZMBH Alliance, a strategic collaboration between the German Cancer Research Center (DKFZ) and the Center for Molecular Biology of Heidelberg University. The research group of Dr. Luke is a member of the Network Aging Research (NAR). This work was initially funded by Heidelberg University’s FRONTIER programme and eventually by the Collaborative Research Centre “Cellular Surveillance and Damage Response” (SFB 1036). Julia Klermund and Katharina Bender are PhD students in the team of Brian Luke.
source : http://www.sciencedaily.com/releases/2014/10/141007131325.htm