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The Radiation Challenge Module 2: Radiation Damage in Living Organisms Educator Guide
National Aeronautics and Space Administration Space Faring The Radiation Challenge An Interdisciplinary Guide on Radiation and Human Space Flight Module 2: Radiation Damage in Living Organisms Educational Product Educators Grades and Students 9 – 12 EP-2007-08-117-MSFC Radiation Educator Guide Module 2: Radiation Damage in Living Organisms Prepared by: Jon Rask, M.S., ARC Education Specialist Wenonah Vercoutere, Ph.D., NASA ARC Subject Matter Expert Al Krause, MSFC Education Specialist BJ Navarro, NASA ARC Project Manager Space Faring: The Radiation Challenge i Table of Contents Module 2: Module 2: Radiation Damage in Living Organisms .............................................................................1 Why is NASA Studying the Biological Effects of Radiation? .........................................................1 How Do Scientists Study Biological Change During Spaceflight? .................................................1 Using Non-Human Organisms to Understand Radiation Damage ................................................2 What are the Risks and Symptoms of Radiation Exposure for Humans? .......................................3 What is DNA? ..............................................................................................................................3 What is the Structure of DNA? .....................................................................................................3 What is DNA’s Role in Protein Production? ..................................................................................4 -
Time, Dose and Fractionation in Radiotherapy
2/25/2013 The introduction of Fractionation 2-13/13 Radiobiology lecture Time, Dose and Fractionation in Radiotherapy The Four Rs of Radiobiology Repair of Sublethal Damage • Cells exposed to sparse radiation experience • Efficacy of fractionation based on the 4 Rs: sublethal injury that can be repaired – Repair of sublethal damage • Cell killing requires a greater total dose when given –Repopulation in several fractions – Reassortment of cells within the cell cycle • Most tissue repair occurs in about 3 hours and up –Reoxygenation to 24 hours post radiation • Allows for repair of injured normal tissue and gives a potential therapeutic advantage over tumor cells Reoxygenation Redistribution • Oxygen stabilizes free radicals • Position in cell cycle at time of radiation • Hypoxic cells require more radiation to kill determines sensitivity •Hypoxic tumors • S phase is radioresistant – Temporary vessel constriction •G2 phase delay results in increased radiation – Outgrowth of blood supply and capillary collapse resistance • Tumor shrinkage reduces hypoxic areas • Fractionated RT redistributes cells • Reinforces fractionated dosing • Rapidly cycling cells like mucosa, skin are more sensitive • Slower cyclers like connective tissue, brain are spared 1 2/25/2013 Repopulation • Increased regeneration of surviving fraction Basics of Fractionation • Rapidly proliferating tumors regenerate faster • Determines the length and timing of therapy course • Dividing a dose into several fractions spares normal tissues • Accelerated Repopulation – Repair -
Extreme Anti-Oxidant Protection Against Ionizing Radiation in Bdelloid Rotifers
Extreme anti-oxidant protection against ionizing radiation in bdelloid rotifers Anita Kriskoa,b, Magali Leroya, Miroslav Radmana,b, and Matthew Meselsonc,1 aInstitut National de la Santé et de la Recherche Médicale Unit 1001, Faculté de Médecine Université Paris Descartes, Sorbonne Paris Cité, 75751 Paris Cedex 15, France; bMediterranean Institute for Life Sciences, 21000 Split, Croatia; and cDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138 Contributed by Matthew Meselson, December 6, 2011 (sent for review November 10, 2011) Bdelloid rotifers, a class of freshwater invertebrates, are extraor- in A. vaga as in other eukaryotes, and its genome is not smaller dinarily resistant to ionizing radiation (IR). Their radioresistance is than that of C. elegans (1). Instead, it has been proposed that a not caused by reduced susceptibility to DNA double-strand break- major contributor to bdelloid radiation resistance is an enhanced age for IR makes double-strand breaks (DSBs) in bdelloids with capacity for scavenging reactive molecular species generated by IR essentially the same efficiency as in other species, regardless of and that the proteins and other cellular components thereby radiosensitivity. Instead, we find that the bdelloid Adineta vaga is protected include those essential for the repair of DSBs but not far more resistant to IR-induced protein carbonylation than is the DNA itself (1). In agreement with this explanation, we find that much more radiosensitive nematode Caenorhabditis elegans.In A. vaga is far more resistant than C. elegans to IR-induced protein both species, the dose–response for protein carbonylation parallels carbonylation, a reaction of hydroxyl radicals with accessible side that for fecundity reduction, manifested as embryonic death. -
Exemplifying an Archetypal Thorium-EPS Complexation by Novel Thoriotolerant Providencia Thoriotolerans
www.nature.com/scientificreports OPEN Exemplifying an archetypal thorium‑EPS complexation by novel thoriotolerant Providencia thoriotolerans AM3 Arpit Shukla 1,2, Paritosh Parmar 1, Dweipayan Goswami 1, Baldev Patel1 & Meenu Saraf 1* It is the acquisition of unique traits that adds to the enigma of microbial capabilities to carry out extraordinary processes. One such ecosystem is the soil exposed to radionuclides, in the vicinity of atomic power stations. With the aim to study thorium (Th) tolerance in the indigenous bacteria of such soil, the bacteria were isolated and screened for maximum thorium tolerance. Out of all, only one strain AM3, found to tolerate extraordinary levels of Th (1500 mg L−1), was identifed to be belonging to genus Providencia and showed maximum genetic similarity with the type strain P. vermicola OP1T. This is the frst report suggesting any bacteria to tolerate such high Th and we propose to term such microbes as ‘thoriotolerant’. The medium composition for cultivating AM3 was optimized using response surface methodology (RSM) which also led to an improvement in its Th‑tolerance capabilities by 23%. AM3 was found to be a good producer of EPS and hence one component study was also employed for its optimization. Moreover, the EPS produced by the strain showed interaction with Th, which was deduced by Fourier Transform Infrared (FTIR) spectroscopy. Te afermaths of atomic bombings of Hiroshima and Nagasaki (1945), more than 2000 nuclear tests (1945–2017), the Chernobyl nuclear power plant disaster (1986) and more recently, the Fukushima Daiichi nuclear disaster (2011), highlight the release of considerable radioactive waste (radwaste) to the environment use of various radionuclides has led to the creation of considerable radioactive waste (radwaste). -
Influence of Radiation Damage on Xenon Diffusion in Silicon Carbide
Influence of radiation damage on xenon diffusion in silicon carbide E. Friedland*a, K. Gärtnerb, T.T. Hlatshwayoa, N.G. van der Berga, T.T. Thabethea a Physics Department, University of Pretoria, Pretoria, South Africa b Institut für Festkörperphysik, Friedrich-Schiller-Universität, Jena, Germany Keywords silicon carbide, diffusion, radiation damage *Corresponding author. E mail: [email protected], Phone: +27-12-4202453, Fax: +27-12-3625288 Diffusion of xenon in poly and single crystalline silicon carbide and the possible influence of radiation damage on it are investigated. For this purpose 360 keV xenon ions were implanted in commercial 6H-SiC and CVD-SiC wafers at room temperature, 350 °C and 600 °C. Width broadening of the implantation pro- files and xenon retention during isochronal and isothermal annealing up to temperatures of 1500 °C was de- termined by RBS-analysis, whilst in the case of 6H-SiC damage profiles were simultaneously obtained by a- particle channelling. No diffusion or xenon loss was detected in the initially amorphized and eventually re- crystallized surface layer of cold implanted 6H-SiC during annealing up to 1200 °C. Above that temperature serious erosion of the implanted surface occurred, which made any analysis impossible. No diffusion or xen- on loss is detected in the hot implanted 6H-SiC samples during annealing up to 1400 °C. Radiation damage dependent grain boundary diffusion is observed at 1300 °C in CVD-SiC. 1 Introduction Modern high-temperature nuclear reactors (HTR’s) commonly use fuel elements containing triple isotropic cladded (TRISO) fuel particles. These are fuel kernels surrounded by four successive lay- ers of low-density pyrolitic carbon, high-density pyrolitic carbon, silicon carbide and high-density pyrolitic carbon, with silicon carbide being the main barrier to prevent the release of fission prod- ucts. -
High Altitude Nuclear Detonations (HAND) Against Low Earth Orbit Satellites ("HALEOS")
High Altitude Nuclear Detonations (HAND) Against Low Earth Orbit Satellites ("HALEOS") DTRA Advanced Systems and Concepts Office April 2001 1 3/23/01 SPONSOR: Defense Threat Reduction Agency - Dr. Jay Davis, Director Advanced Systems and Concepts Office - Dr. Randall S. Murch, Director BACKGROUND: The Defense Threat Reduction Agency (DTRA) was founded in 1998 to integrate and focus the capabilities of the Department of Defense (DoD) that address the weapons of mass destruction (WMD) threat. To assist the Agency in its primary mission, the Advanced Systems and Concepts Office (ASCO) develops and maintains and evolving analytical vision of necessary and sufficient capabilities to protect United States and Allied forces and citizens from WMD attack. ASCO is also charged by DoD and by the U.S. Government generally to identify gaps in these capabilities and initiate programs to fill them. It also provides support to the Threat Reduction Advisory Committee (TRAC), and its Panels, with timely, high quality research. SUPERVISING PROJECT OFFICER: Dr. John Parmentola, Chief, Advanced Operations and Systems Division, ASCO, DTRA, (703)-767-5705. The publication of this document does not indicate endorsement by the Department of Defense, nor should the contents be construed as reflecting the official position of the sponsoring agency. 1 Study Participants • DTRA/AS • RAND – John Parmentola – Peter Wilson – Thomas Killion – Roger Molander – William Durch – David Mussington – Terry Heuring – Richard Mesic – James Bonomo • DTRA/TD – Lewis Cohn • Logicon RDA – Les Palkuti – Glenn Kweder – Thomas Kennedy – Rob Mahoney – Kenneth Schwartz – Al Costantine – Balram Prasad • Mission Research Corp. – William White 2 3/23/01 2 Focus of This Briefing • Vulnerability of commercial and government-owned, unclassified satellite constellations in low earth orbit (LEO) to the effects of a high-altitude nuclear explosion. -
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Downloaded by guest on September 29, 2021 Proc. Nati. Acad. Sci. USA Vol. 88, pp. 10652-10656, December 1991 Genetics Role of transfection and clonal selection in mediating radioresistance (gene transfer/radiosensitivity/neomycin/oncogenes) FRANCISCO S. PARDO*t, ROBERT G. BRISTOWt, ALPHONSE TAGHIAN*, AUGUSTINUS ONG§, AND CARMIA BOREK§ *Department of Radiation Oncology, Massachusetts General Hospital/Harvard Medical School, Boston, MA 02114; SPrincess Margaret Hospital, Toronto, ON Canada; and §Division of Radiation and Cancer Biology, Department of Radiation Oncology, Tufts University School of Medicine/New England Medical Center, Boston, MA 02111 Communicated by Harry Rubin, August 12, 1991 ABSTRACT Transfected oncogenes have been reported to is a radiobiologically well-characterized early-passage glio- increase the radioresistance of rodent cells. Whether trans- blastoma cell line, established from human operative material, fected nononcogenic DNA sequences and subsequent clonal at Massachusetts General Hospital. Immunoperoxidase data selection can result in radioresistant cell populations is un- for glial fibrillary acidic protein substantiates its glial origin known. The present set of experiments describe the in vitro (F.S.P., unpublished data). Subclones ofthe parental glioblas- radiosensitivity and tumorigenicity of selected clones of pri- toma cells were established from the initial tumor biopsy. All mary rat embryo cells and human glioblastoma cells, after cultures were passaged and maintained in Dulbecco's modi- transfection with a neomycin-resistance marker (pSV2neo or fied Eagle's medium (DMEM, Sigma) fortified with 10o pCMVneo) and clonal selection. Radiobiological data compar- (vol/vol) fetal calf serum (Rehatuin, St. Louis). Cells were ing the surviving fraction at 2 Gy (SF2) and the mean inacti- incubated in a humidified atmosphere of 5% C02/95% air at vation dose show the induction of radioresistance in two rat 37°C. -
Radiobiology Is a Young Science and Is Solely Concerned with the Study Of
The Rockefeller Foundation and its support of Radiobiology up to the 1970s By Sinclair Wynchank Senior Lecturer University of Cape Town Rondebosch, South Africa [email protected] © 2011 by Sinclair Wynchank Radiation biology, or radiobiology, is a very young science, solely concerned with the study of the interactions between ionizing radiation and living matter. This science slowly became a recognized field of study after the discovery of ionizing radiation (i.e., X rays) in 1895. A broadly varied and evolving terminology has been applied to aspects of radiobiology and therefore, archival searches concerning it are complex. This report is a work in progress, which mainly recounts support given by the Rockefeller Foundation (RF) to radiobiology. The RF was a most important player in the early history of radiobiology and a crucial influence in ensuring that the science steadily matured during its first six decades. Time constraints prevented all relevant items from being accessed, but a clear idea of the RF‟s strong influence on radiobiology‟s early history has resulted. Examples of RF activities to verify this assertion are given below, in by and large chronological order. After a brief analysis of RF aid, there is a short account of why its support so strongly benefitted the young science. To my knowledge there is very little written about the history of radiobiology and nothing about the role that the RF or other philanthropic bodies played in this history. Inevitably, for an extensive time, individual radiobiologists first studied other fields of science before radiobiology. Even in 2011 there are only five universities in the U.S. -
Research Status on Radiation Damage in Nuclear Materials and Recommendations for Iaea Activities
XA0202570 IC/IR/2002/4 INTERNAL REPORT (Limited Distribution) United Nations Educational Scientific and Cultural Organization and International Atomic Energy Agency THE ABDUS SALAM INTERNATIONAL CENTRE FOR THEORETICAL PHYSICS RESEARCH STATUS ON RADIATION DAMAGE IN NUCLEAR MATERIALS AND RECOMMENDATIONS FOR IAEA ACTIVITIES TECHNICAL REPORT Alfredo Caro and Magdalena Caro Centro Atomico Bariloche, 8400 Bariloche, Argentina and The Abdus Salam International Centre for Theoretical Physics, Trieste, Italy. MIRAMARE - TRIESTE March 2002 3 3/ IC/2002/19 United Nations Educational Scientific and Cultural Organization and International Atomic Energy Agency THE ABDUS SALAM INTERNATIONAL CENTRE FOR THEORETICAL PHYSICS RESEARCH STATUS ON RADIATION DAMAGE IN NUCLEAR MATERIALS AND RECOMMENDATIONS FOR IAEA ACTIVITIES TECHNICAL REPORT Alfredo Caro and Magdalena Caro Centro Atomico Bariloche, 8400 Bariloche, Argentina and The Abdus Salam International Centre for Theoretical Physics, Trieste, Italy. MIRAMARE - TRIESTE March 2002 Contents Foreword 3 Introduction 4 State of the art in the area Technological standpoint 4 Scientific perspectives 10 Recommendations for IAEA activities 18 Examples of research areas 20 Deliverables 22 Conclusions 22 References 22 Foreword On the basis of the exchange of ideas that the authors have had since July 2000 with Prof. Yu Lu of the Abdus Salam International Centre for Theoretical Physics, and with Drs. W. Burkart and D. Muir of the International Atomic Energy Agency, we present a report on the present status of the technological and scientific aspects of embrittlement of nuclear reactor pressure vessels, together with our advise on what could be the concerted action between the Abdus Salam ICTP and IAEA aiming at the promotion of research activities in the field of materials science, particularly focused in issues relevant to nuclear applications. -
Chapter 5 Biological Effects of Ionizing Radiation Page I
CHAPTER 5 BIOLOGICAL EFFECTS OF IONIZING RADIATION PAGE I. Introduction ............................................................................................................................ 5-3 II. Mechanisms of Radiation Damage ........................................................................................ 5-3 A. Direct Action .............................................................................................................. 5-3 B. Indirect Action ........................................................................................................... 5-3 III. Determinants of Biological Effects ........................................................................................ 5-4 A. Rate of Absorption ..................................................................................................... 5-5 B. Area Exposed ............................................................................................................. 5-5 C. Variation in Species and Individual Sensitivity ......................................................... 5-5 D. Variation in Cell Sensitivity ....................................................................................... 5-5 IV. The Dose-Response Curve ..................................................................................................... 5-6 V. Pattern of Biological Effects .................................................................................................. 5-7 A. Prodromal Stage ........................................................................................................ -
Radioresistance of Brain Tumors
cancers Review Radioresistance of Brain Tumors Kevin Kelley 1, Jonathan Knisely 1, Marc Symons 2,* and Rosamaria Ruggieri 1,2,* 1 Radiation Medicine Department, Hofstra Northwell School of Medicine, Northwell Health, Manhasset, NY 11030, USA; [email protected] (K.K.); [email protected] (J.K.) 2 The Feinstein Institute for Molecular Medicine, Hofstra Northwell School of Medicine, Northwell Health, Manhasset, NY 11030, USA * Correspondence: [email protected] (M.S.); [email protected] (R.R.); Tel.: +1-516-562-1193 (M.S.); +1-516-562-3410 (R.R.) Academic Editor: Zhe-Sheng (Jason) Chen Received: 17 January 2016; Accepted: 24 March 2016; Published: 30 March 2016 Abstract: Radiation therapy (RT) is frequently used as part of the standard of care treatment of the majority of brain tumors. The efficacy of RT is limited by radioresistance and by normal tissue radiation tolerance. This is highlighted in pediatric brain tumors where the use of radiation is limited by the excessive toxicity to the developing brain. For these reasons, radiosensitization of tumor cells would be beneficial. In this review, we focus on radioresistance mechanisms intrinsic to tumor cells. We also evaluate existing approaches to induce radiosensitization and explore future avenues of investigation. Keywords: radiation therapy; radioresistance; brain tumors 1. Introduction 1.1. Radiotherapy and Radioresistance of Brain Tumors Radiation therapy is a mainstay in the treatment of the majority of primary tumors of the central nervous system (CNS). However, the efficacy of this therapeutic approach is significantly limited by resistance to tumor cell killing after exposure to ionizing radiation. This phenomenon, termed radioresistance, can be mediated by factors intrinsic to the cell or by the microenvironment. -
General Guidelines for the Estimation of Committed Effective Dose from Incorporation Monitoring Data
Forschungszentrum Karlsruhe in der Helmholtz-Gemeinschaftt Wissenschaftliche Berichte FZKA 7243 General Guidelines for the Estimation of Committed Effective Dose from Incorporation Monitoring Data (Project IDEAS – EU Contract No. FIKR-CT2001-00160) H. Doerfel, A. Andrasi, M. Bailey, V. Berkovski, E. Blanchardon, C.-M. Castellani, C. Hurtgen, B. LeGuen, I. Malatova, J. Marsh, J. Stather Hauptabteilung Sicherheit August 2006 Forschungszentrum Karlsruhe in der Helmholtz-Gemeinschaft Wissenschaftliche Berichte FZKA 7243 GENERAL GUIDELINES FOR THE ESTIMATION OF COMMITTED EFFECTIVE DOSE FROM INCORPORATION MONITORING DATA (Project IDEAS – EU Contract No. FIKR-CT2001-00160) H. Doerfel, A. Andrasi 1, M. Bailey 2, V. Berkovski 3, E. Blanchardon 6, C.-M. Castellani 4, C. Hurtgen 5, B. LeGuen 7, I. Malatova 8, J. Marsh 2, J. Stather 2 Hauptabteilung Sicherheit 1 KFKI Atomic Energy Research Institute, Budapest, Hungary 2 Health Protection Agency, Radiation Protection Division, (formerly National Radiological Protection Board), Chilton, Didcot, United Kingdom 3 Radiation Protection Institute, Kiev, Ukraine 4 ENEA Institute for Radiation Protection, Bologna, Italy 5 Belgian Nuclear Research Centre, Mol, Belgium 7 Institut de Radioprotection et de Sûreté Nucléaire, Fontenay-aux-Roses, France 8 Electricité de France (EDF), Saint-Denis, France 9 National Radiation Protection Institute, Praha, Czech Republic Forschungszentrum Karlsruhe GmbH, Karlsruhe 2006 Für diesen Bericht behalten wir uns alle Rechte vor Forschungszentrum Karlsruhe GmbH Postfach 3640, 76021 Karlsruhe Mitglied der Hermann von Helmholtz-Gemeinschaft Deutscher Forschungszentren (HGF) ISSN 0947-8620 urn:nbn:de:0005-072434 IDEAS General Guidelines – June 2006 Abstract Doses from intakes of radionuclides cannot be measured but must be assessed from monitoring, such as whole body counting or urinary excretion measurements.