New advances in radiation biology.

Current understanding of risk associated with low-dose radiation exposure has for many years been embedded in the linear-no-threshold (LNT) approach, based on simple extrapolation from the Japanese atomic bomb survivors. Radiation biology research has supported the LNT approach although much of this has been limited to relatively high-dose studies. Recently, with new advances for studying effects of low-dose exposure in experimental models and advances in molecular and cellular biology, a range of new effects of biological responses to radiation has been observed. These include genomic instability, adaptive responses and bystander effects. Most have one feature in common in that they are observed at low doses and suggest significant non-linear responses. These new observations pose a significant challenge to our understanding of low-dose exposure and require further study to elucidate mechanisms and determine their relevance.

[1]  左雅慧,et al.  Non-targeted and delayed effects of exposure to ionizing radiation , 2007 .

[2]  Joseph M Kaminski,et al.  The controversial abscopal effect. , 2005, Cancer treatment reviews.

[3]  B. Vojnovic,et al.  New insights into the cellular response to radiation using microbeams , 2005 .

[4]  Nesrin Asaad,et al.  Medium-mediated intercellular communication is involved in bystander responses of X-ray-irradiated normal human fibroblasts , 2005, Oncogene.

[5]  Kevin M Prise,et al.  Targeted cytoplasmic irradiation induces bystander responses. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[6]  R. Preston,et al.  RADIATION BIOLOGY: CONCEPTS FOR RADIATION PROTECTION , 2004, Health physics.

[7]  K. Prise,et al.  Nitric oxide-mediated signaling in the bystander response of individually targeted glioma cells. , 2003, Cancer research.

[8]  R. Doll,et al.  Cancer risks attributable to low doses of ionizing radiation: Assessing what we really know , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[9]  M. Kadhim Role of genetic background in induced instability , 2003, Oncogene.

[10]  Y. Dubrova Radiation-induced transgenerational instability , 2003, Oncogene.

[11]  E. Wright,et al.  Radiation-induced genomic instability and bystander effects: inter-related nontargeted effects of exposure to ionizing radiation , 2003, Oncogene.

[12]  M. Bittner,et al.  Functional genomics as a window on radiation stress signaling , 2003, Oncogene.

[13]  W. Morgan,et al.  Non-targeted and Delayed Effects of Exposure to Ionizing Radiation: II. Radiation-Induced Genomic Instability and Bystander Effects In Vivo, Clastogenic Factors and Transgenerational Effects , 2003, Radiation research.

[14]  W. Morgan Non-targeted and Delayed Effects of Exposure to Ionizing Radiation: I. Radiation-Induced Genomic Instability and Bystander Effects In Vitro , 2003, Radiation research.

[15]  K. Camphausen,et al.  Radiation abscopal antitumor effect is mediated through p53. , 2003, Cancer research.

[16]  Edouard I Azzam,et al.  Oxidative metabolism modulates signal transduction and micronucleus formation in bystander cells from alpha-particle-irradiated normal human fibroblast cultures. , 2002, Cancer research.

[17]  W. Dewey,et al.  Historical and Current Highlights in Radiation Biology: Has Anything Important Been Learned by Irradiating Cells? , 2002, Radiation research.

[18]  岩崎 民子 SOURCES AND EFFECTS OF IONIZING RADIATION : United Nations Scientific Committee on the Effects of Atomic Radiation UNSCEAR 2000 Report to the General Assembly, with Scientific Annexes , 2002 .

[19]  M. Barcellos-Hoff,et al.  Extracellular Signaling through the Microenvironment: A Hypothesis Relating Carcinogenesis, Bystander Effects, and Genomic Instability , 2001, Radiation research.

[20]  Noelle F. Metting,et al.  Adaptive Response and the Bystander Effect Induced by Radiation in C3H 10T½ Cells in Culture , 2001, Radiation research.

[21]  D. Brenner,et al.  The Bystander Effect in Radiation Oncogenesis: I. Transformation in C3H 10T½ Cells In Vitro can be Initiated in the Unirradiated Neighbors of Irradiated Cells , 2001, Radiation research.

[22]  J. Little,et al.  Direct evidence for the participation of gap junction-mediated intercellular communication in the transmission of damage signals from alpha -particle irradiated to nonirradiated cells. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[23]  A. Upton Radiation Hormesis: Data and Interpretations , 2001, Critical reviews in toxicology.

[24]  J. Battista,et al.  In-field and out-of-field effects in partial volume lung irradiation in rodents: possible correlation between early dna damage and functional endpoints. , 2000, International journal of radiation oncology, biology, physics.

[25]  Sally A. Amundson,et al.  Identification of Potential mRNA Biomarkers in Peripheral Blood Lymphocytes for Human Exposure to Ionizing Radiation , 2000, Radiation research.

[26]  B. Lehnert,et al.  Factors underlying the cell growth-related bystander responses to alpha particles. , 2000, Cancer research.

[27]  J. Little,et al.  Unexpected sensitivity to the induction of mutations by very low doses of alpha-particle radiation: evidence for a bystander effect. , 1999, Radiation research.

[28]  D. Boreham,et al.  The adaptive response modifies latency for radiation-induced myeloid leukemia in CBA/H mice. , 1999, Radiation research.

[29]  Donald A. Jackson,et al.  Occupational radiation exposure and mortality: second analysis of the National Registry for Radiation Workers , 1999, Journal of radiological protection : official journal of the Society for Radiological Protection.

[30]  K M Prise,et al.  Studies of bystander effects in human fibroblasts using a charged particle microbeam. , 1998, International journal of radiation biology.

[31]  D. Goodhead,et al.  Chromosomal instability in the descendants of unirradiated surviving cells after alpha-particle irradiation. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[32]  J. Van Dyk,et al.  Partial volume rat lung irradiation: an evaluation of early DNA damage. , 1998, International journal of radiation oncology, biology, physics.

[33]  G Vergnaud,et al.  Further evidence for elevated human minisatellite mutation rate in Belarus eight years after the Chernobyl accident. , 1997, Mutation research.

[34]  M. Kadhim,et al.  Genetic factors influencing alpha-particle-induced chromosomal instability. , 1997, International journal of radiation biology.

[35]  S. Wolff Aspects of the adaptive response to very low doses of radiation and other agents. , 1996, Mutation research.

[36]  E Cardis,et al.  Effects of low doses and low dose rates of external ionizing radiation: cancer mortality among nuclear industry workers in three countries. , 1995, Radiation research.

[37]  J. Little,et al.  Induction of sister chromatid exchanges by extremely low doses of alpha-particles. , 1992, Cancer research.

[38]  D. T. Goodhead,et al.  Transmission of chromosomal instability after plutonium α-particle irradiation , 1992, Nature.

[39]  S. Wolff,et al.  Adaptive response of human lymphocytes to low concentrations of radioactive thymidine. , 1984, Science.

[40]  R. McClellan,et al.  The induction of liver tumors by 239Pu citrate or 239PuO2 particles in the Chinese hamster. , 1983, Radiation research.

[41]  R. McClellan,et al.  Effect of 239PuO2 particle number and size on the frequency and distribution of chromosome aberrations in the liver of the Chinese hamster. , 1974, Radiation research.

[42]  T. Puck,et al.  ACTION OF X-RAYS ON MAMMALIAN CELLS , 1956, The Journal of experimental medicine.

[43]  M. Ahram,et al.  A proteomic approach to characterize protein shedding , 2005, Proteomics.

[44]  M. Kadhim,et al.  Studies of targeted effects on human lymphocytes using a charged-particle microbeam , 2000 .

[45]  T G Myers,et al.  The complexity of radiation stress responses: analysis by informatics and functional genomics approaches. , 1999, Gene expression.

[46]  C. Mothersill,et al.  Delayed expression of lethal mutations and genomic instability in the progeny of human epithelial cells that survived in a bystander-killing environment. , 1997, Radiation oncology investigations.

[47]  C. Mothersill,et al.  Medium from irradiated human epithelial cells but not human fibroblasts reduces the clonogenic survival of unirradiated cells. , 1997, International journal of radiation biology.

[48]  I. Emerit Reactive oxygen species, chromosome mutation, and cancer: possible role of clastogenic factors in carcinogenesis. , 1994, Free radical biology & medicine.

[49]  D T Goodhead,et al.  Transmission of chromosomal instability after plutonium alpha-particle irradiation. , 1992, Nature.

[50]  K. Trott,et al.  Intraclonal recovery of division probability in pedigrees of single x-irradiated mammalian cells. , 1970, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[51]  L. Thompson,et al.  Proliferation kinetics of x-irradiated mouse L cells studied WITH TIME-lapse photography. II. , 1969, International journal of radiation biology and related studies in physics, chemistry, and medicine.