As a result of various stresses, lesions caused by DNA-damaging agents occur constantly in each cell of the human body. Generally, DNA damage is recognized and repaired by the DNA damage response (DDR) machinery, and the cells survive. When repair fails, the genomic integrity of the cell is disrupted-a hallmark of cancer. In addition, the DDR plays a dual role in cancer development and therapy....

Genome integrity is constantly monitored by sophisticated cellular networks, collectively termed the DNA damage response (DDR). A common feature of DDR proteins is their mobilization in response to genotoxic stress. Here, we outline how the development of various complementary methodologies has provided valuable insights into the spatiotemporal dynamics of DDR protein assembly/disassembly at si...

A major issue in aging research is how cellular phenomena affect aging at the systemic level. Emerging evidence suggests that DNA damage response (DDR) signaling is a key mechanism linking DNA damage accumulation, cell senescence, and organism aging. DDR activation in senescent cells promotes acquisition of a proinflammatory secretory phenotype (SASP), which in turn elicits DDR and SASP activat...

p53, apoptosis, and senescence are frequently activated in preneoplastic lesions and are barriers to progression to malignancy. These barriers have been suggested to result from an ATM-mediated DNA damage response (DDR), which may follow oncogene-induced hyperproliferation and ensuing DNA replication stress. To elucidate the currently untested role of DDR in breast cancer initiation, we examine...

8. The Outbreak Investigation Team was (in Alphabetical order): Jenny Barralet (Qld), Robert Bell (Qld), Andrew Black (ACT), Gerard Fitzsimmons (DoHA), Joy Gregory (Vic), Rachel Hanson (Vic), Melissa Irwin (NSW), Martyn Kirk (DoHA), Karin Lalor (Vic), Dot Little (Hunter, New England), Tony Merritt (Hunter New England), Sally Munnoch (Hunter New England), Leonie Neville (NSW), Rhonda Owen (DoHA)...

The OzFoodNet Working Group is (in alphabetical order): Jenny Barralet (Qld), Robert Bell (Qld), Andrew Black (ACT), Barry Combs (SA), Craig Dalton (Hunter New England), Gerard Fitzsimmons (DoHA), Joy Gregory (Vic), Gillian Hall (NCEPH), Brigid Hardy (DAFF), Geoff Hogg (MDU), Melissa Irwin (NSW), Martyn Kirk (DoHA), Karin Lalor (Vic), Deon Mahoney (FSANZ), Tony Merritt (Hunter New England), Ros...

DNA damage response (DDR) is the critical surveillance mechanism in maintaining genome integrity. The mechanism activates checkpoints to prevent cell cycle progression in the presence of DNA lesions, and mediates lesion repair. DDR is coordinated by three apical PI3 kinase related kinases (PIKKs), including ataxia-telangiectasia mutated (ATM), ATM- and Rad3-related (ATR), and DNA-PKcs (the cata...

The DNA damage response (DDR) represents a complex network of multiple signaling pathways involving cell cycle checkpoints, DNA repair, transcriptional programs, and apoptosis, through which cells maintain genomic integrity following various endogenous (metabolic) or environmental stresses. In cancer treatment, the DDR occurs in response to various genotoxic insults by diverse cytotoxic agents ...