Skip to main content

Cellular and Molecular Effects of Radon and Other Alpha Particle Emitters

  • Chapter

Part of the book series: Advances in Mutagenesis Research ((MUTAGENESIS,volume 3))

Abstract

It has long been known that the inhalation of radon gas induces lung cancer, as indicated by evidence provided by epidemiological studies of uranium (R.D. Evans et al. 1981; Samet 1989; Samet et al. 1989) and tin (Lubin et al. 1990) miners as well as by studies using experimental animals (Cross et al. 1985; Lafuma et al. 1989). The induction of lung cancer increases linearly with dose, and the efficiency of induction increases with a decrease in the exposure rate (Little et al. 1985; BEIR IV Report 1988; Lubin et al. 1990; Moolgavcar et al. 1990). However, the realization that indoor radon can reach levels sufficient to cause a significant increase in the risk of lung cancer for the general population became an issue of concern in 1986, when engineer Stanley Watras set off the radiation monitor at the Limerick nuclear power plant in eastern Pennsylvania. Subsequent measurements showed radon levels in his home amounting to 2700 pCi/l, a level markedly higher than that experienced by the majority of uranium miners (10–20 pCi/l), and decidedly higher than the estimated average US indoor radon level of 1.5 pCi/l (Nero et al. 1986). It has been calculated that as many as 16 000 of the 140 000 cases of lung cancer occurring annually in the United States may result from the inhalation of radon (Brenner 1989).

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   84.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Aghamohammadi SZ, Goodhead DT, Savage JRK (1988) Induction of sister chromatid exchanges (SCE) in Go lymphocytes by plutonium-238 a-particles. Int J Radiat Biol 53:909–915

    Google Scholar 

  • Aufderheide E, Rink H, Hieber L, Kraft G (1987) Heavy ion effects on cellular DNA: strand break induction and repair in cultured diploid lens epithelial cells. Int J Radiat Biol 51:779–790

    Google Scholar 

  • Barendsen GW (1962) Dose-survival curves of human cells in tissue culture irradiated with alpha-, beta-, 20-kV X-, and 200-kV X radiation. Nature 193:1153–1155

    Google Scholar 

  • Barendsen GW (1990) Mechanisms of cell reproductive death and shapes of radiation dose-survival curves of mammalian cells. Int J Radiat Biol 57:885–896

    Google Scholar 

  • Bedford JS, Goodhead DT (1989) Breakage of human interphase chromosomes by alpha particles and X-rays. Int J Radiat Biol 55:211–216

    Google Scholar 

  • BEIR IV (1988) Health risks of radon and other internally deposited alpha emitters. National Research Council, National Academy Press, Washington, D.C., Chapter 2, pp 112, 442

    Google Scholar 

  • Belli M, Cherubini R, Finotto S, Moschini G, Sapora O, Simone G, Tabocchini MA (1989) RBE-LET relationship for the survival of V79 cells irradiated with low energy protons. Int J Radiat Biol 55:93–104

    Google Scholar 

  • Benedict WF, Murphree AL, Banerjee A, Sparkes MC, Sparkes RS (1983) Patient with 13 chromosome deletion: evidence that the retinoblastoma gene is a recessive cancer gene. Science 219:973–975

    Google Scholar 

  • Bertsche U (1978) The response of diploid yeast to radiations at different LET 1. Potentially lethal and lethal damage to reproductive capacity. Radiat Res 76:349–367

    Google Scholar 

  • Bilbao A, Prosser JS, Edwards AA, Moody JC, Lloyd DC (1989) The induction of micronuclei in human lymphocytes by in vitro irradiation with alpha particles from plutonium-239. Int J Radiat Biol 56:287–292

    Google Scholar 

  • Billings PC, Shuin T, Lillehaug J, Miura T, Roy-Burman P, Landolph JR (1987J Enhanced expression and state of the i-my oncogene in chemically and X-ray-transformed C3H/10T1/2 CI 8 mouse embryo fibroblasts. Cancer Res 47:3643–3649

    Google Scholar 

  • Bird RP, Zaider M, Rossi HH, Hall EJ, Marino SA, Rohrig N (1983) The sequential irradiation of mammalian cells with X rays and charged particles of high LET. Radiat Res 93:444–452

    Google Scholar 

  • Birrer MJ, Minna JD (1989) Genetic changes in the pathogenesis of lung cancer. Annu Rev Med 40:305–317

    Google Scholar 

  • Bishop JM (1987) The molecular genetics of cancer. Science 235:305–311

    Google Scholar 

  • Blocher D (1988) DNA double-strand break repair determines the RBE of a-particles. Int J Radiat Biol 54:761–771

    Google Scholar 

  • Bonev MN, Kozubek S, Krasavin EA, Amirtajev KG (1990) Prophage induction in repair-deficient and wild-type E. coli strains by y-rays and heavy ions. Int J Radiat Biol 57:993–1005

    Google Scholar 

  • Borek C, Hall EJ, Rossi HH (1978) Malignant transformation in cultured hamster embryo cells produced by X-rays, 430-keV monoenergetic neutrons, and heavy ions. Cancer Res 38:2997–3005

    Google Scholar 

  • Borek C, Ong A, Mason H (1987) Distinctive transforming genes in X-ray-transformed mammalian cells. Proc Natl Acad Sci USA 84:794–798

    Google Scholar 

  • Brandom WF, Saccomanno G, Archer VE, Archer PG, Bloom AD (1978) Chromosome aberrations as a biological dose-response indicator of radiation exposure in uranium miners. Radiat Res 76:159–171

    Google Scholar 

  • Brenner DJ (1989) Radon Risk and Remedy. W. H. Freeman, New York, p 102

    Google Scholar 

  • Brown R, Thacker J (1984) The nature of mutants induced by ionising radiation in cultured hamster cells. I. Isolation and initial characterisation of spontaneous, ionising radiation-induced, and ethyl methanesulphonate-induced mutants resistant to 6-thioguanine. Mutat Res 129:269–281

    Google Scholar 

  • Charlton DE, Nikjoo H, Humm JL (1989) Calculation of initial yields of single- and double-strand breaks in cell nuclei from electrons, protons and alpha particles. Int J Radiat Biol 56:1–19

    Google Scholar 

  • Chen DJ, Strniste GF, Tokita N (1984) The genotoxicity of alpha particles in human embryonic skin fibroblasts. Radiat Res 100:321–327

    Google Scholar 

  • Chen DJ, Hanks T, Carpenter S (1991) Mutagenic effects of a particles. In: Cross FT (ed) Indoor radon and lung cancer: reality or myth? 29th Hanford Symposium on Health and the Environment. Battelle Press, Richland, WA (in press)

    Google Scholar 

  • Cole A, Shonka F, Corry P, Cooper WG (1975) CHO cell repair of single-strand and double-strand DNA breaks induced by and a radiations. In: Hanawalt PC, Setlow RB (eds) Molecular mechanisms for repair of DNA. Plenum, New York, vol 5B, pp 665–676

    Google Scholar 

  • Cole NJ, Nowell PC (1965) Radiation carcinogenesis: the sequence of events. Science 150:1782- 1786

    Google Scholar 

  • Coquerelle TM, Weibezahn KF, Liicke-Huhle C (1987) Rejoining of double strand breaks in normal human and ataxia-telangiectasia fibroblasts after exposure to sup60Co y-rays, sup241 Am a-particles or bleomycin. Int J Radiat Biol 51:209–218

    Google Scholar 

  • Cornforth MN (1989) On the nature of interactions leading to radiation-induced chromosomal exchange. Int J Radiat Biol 56:635–643

    Google Scholar 

  • Cornforth MN (1990) Cytogenetic damage in human fibroblasts induced with a radon-model exposure system. Symposium presented at the 38th annual meeting of the Radiation Research Society, New Orleans

    Google Scholar 

  • Cox R, Masson WK (1978) Do radiation-induced thioguanine-resistant mutants of cultured mammalian cells arise by HGPRT gene mutation or X chromosome rearrangement? Nature 276:629–630

    Google Scholar 

  • Cox R, Masson WK (1979) Mutation and inactivation of cultured mammalian cells exposed to beams of accelerated heavy ions III. Human diploid fibroblasts. Int J Radiat Biol 36:149–160

    Google Scholar 

  • Cox R, Thacker J, Goodhead DT, Munson RJ (1977) Mutation and inactivation of mammalian cells by various ionising radiations. Nature 267:425–427

    Google Scholar 

  • Cross FT, Harley NH, Hofmann W (1985) Health effects and risks from in drinking water. Health Phys 48:649–670

    Google Scholar 

  • Curtis SB (1986) Lethal and potentially lethal lesions induced by radiation — a unified repair model. Radiat Res 106:252–270

    Google Scholar 

  • Das G, Stewart JW, Sherman F (1986) Mutational alterations induced in yeast by ionizing radiation. Mutat Res 163:233–245

    Google Scholar 

  • DeMarini DM, Brockman HE, de Serres FJ, Evans HH, Stankowski LF Jr, Hsie AW (1989) Specific- locus mutations induced in eukaryotes (especially mammalian cells) by radiation and chemicals: a perspective. Mutat Res 220:11–29

    Google Scholar 

  • de Serres FJ, Webber BB, Lyman JT (1967) Mutation-induction and nuclear inactivation in Neurospora crassa using radiations with different rates of energy loss. Radiat Res Suppl 7:160–171

    Google Scholar 

  • Diamond LE, Guerrero I, Pellicer A (1988) Concomitant K- and N-ras gene point mutations in clonal murine lymphomas. Mol Cell Biol 8:2233–2236

    Google Scholar 

  • Edwards AA, Purrott RJ, Prosser JS, Lloyd DC (1980) The induction of chromosome aberrations in human lymphocytes by alpha-radiation. Int J Radiat Biol 38:83–91

    Google Scholar 

  • Endlich BP, Ling CC (1986) Cotransformation of rat embryo cells with transfected oncogenes and X-rays. Presented at the 35th annual meeting of the Radiation Research Society, Atlanta

    Google Scholar 

  • Evans HH, Mencl J, Horng MF, Ricanati M, Sanchez C, Hozier J (1986) Locus specificity in the mutability of L5178Y mouse lymphoma cells: the role of multilocus lesions. Proc Natl Acad Sci USA 83:4379–4383

    Google Scholar 

  • Evans HH, Ricanati M, Horng MF (1987) Deficiency in DNA repair in mouse lymphoma strain L5178Y-S. Proc Natl Acad Sci USA 84:7562–7566

    Google Scholar 

  • Evans RD, Harley JH, Jacobi W, McLean AS, Mills WA, Stewart CG (1981) Estimate of risk from environmental exposure to radon-222 and its decay products. Nature 290:99–100

    Google Scholar 

  • Farber E, Cameron R (1980) The sequential analysis of cancer development. Adv Cancer Res 31:125- 226

    Google Scholar 

  • Felber M, Sawey MJ, Garte SJ (1987) Molecular cloning of an activated c-myc oncogene from a radiation-induced rat skin carcinoma. Proc Annu Meet Am Assoc Cancer Res 28:460

    Google Scholar 

  • Fox JC, McNally NJ (1990) The rejoining of DNA double-strand breaks following irradiation with Pu a-particles: evidence for a fast component of repair as measured by neutral filter elution. Int J Radiat Biol 57:513–521

    Google Scholar 

  • Frankenberg D, Frankenberg-Schwager D, Blocher D, Harbich R (1981) Evidence for DNA double- strand breaks as the critical lesions in yeast cells irradiated with sparsely or densely ionizing radiation under oxic or anoxic conditions. Radiat Res 88:524–532

    Google Scholar 

  • Frankenberg-Schwager M, Frankenberg D, Harbich R (1984) Repair of double-strand breaks as a determinant of RBE of alpha particles. Br J Cancer 49 Suppl VI: 169–173

    Google Scholar 

  • Frankenberg-Schwager M, Frankenberg D, Harbich R, Adamczyk C (1990) A comparative study of rejoining of DNA double-strand breaks in yeast irradiated with 3.5 MeV a-particles or with 30 MeV electrons. Int J Radiat Biol 57:1151–1168

    Google Scholar 

  • Frazier ME, Seed TM, Whiting LL, Steigler GL (1988) Evidence for oncogene activation in radiation induced carcinogenesis. In: Park JF, Pelroy RA (eds) Multilevel health effects research: from molecules to man. 27th Hanford Symposium on Health and the Environment. Battelle Press, Richland, WA, pp 197–205

    Google Scholar 

  • Garte SJ, Sawey MJ, Burns FJ, Felber M, Ashkenazi-Kimmel T (1987) Multiple oncogene activation in a radiation carcinogenesis model. In: Cerrutti PA, Nygaard OF, Simic ME (eds) Anti- carcinogenesis and radiation protection. Plenum, New York, pp 341–344

    Google Scholar 

  • Geard C (1980) Initial changes in cell cycle progression of Chinese hamster V-79 cells induced by high-LET charged particles. Radiat Res 83:696–709

    Google Scholar 

  • Geard C (1985) Charged particle cytogenetics: effects of LET, fluence, and particle separation on chromosome aberrations. Radiat Res 104:SI 12-S121

    Google Scholar 

  • Geard C, Jenkins G, Jones J (1990) Dose dependent induction of mutation by ionising radiations in CHO-AS52 cells: effects of high and low dose rate gamma rays, delayed plating and high LET alpha particles. Environ Mol Mutagen 15:S7-S21

    Google Scholar 

  • Giaccia A, Weinstein R, Hu J, Stamato TD (1985) Cell cycle-dependent repair of double-strand breaks in a y ray-sensitive Chinese hamster cell. Somat Cell Mol Genet 11:485–491

    Google Scholar 

  • Glickman BW, Ripley LS (1984) Structural intermediates of deletion mutagenesis: a role for palindromic DNA. Proc Natl Acad Sci USA 81:512–516

    Google Scholar 

  • Godbout R, Dryja TP, Squire J, Gallie BL, Phillips RA (1983) Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma. Nature 304:451–453

    Google Scholar 

  • Goodhead DT (1985) Saturable repair models of radiation action in mammalian cells. Radiat Res 104:558–567

    Google Scholar 

  • Goodhead DT (1989) The initial physical damage produced by ionizing radiations. Int J Radiat Biol 56:623–634

    Google Scholar 

  • Goodhead DT (1990) Radiation effects in living cells. Can J Physics 68:872–886

    Google Scholar 

  • Goodhead DT, Nikjoo H (1989) Track structure analysis of ultrasoft X-rays compared to high-and low-LET radiations. Int J Radiat Biol 55:513–529

    Google Scholar 

  • Goodhead DT, Munson RJ, Thacker J, Cox R (1980) Mutation and inactivation of cultured mammalian cells exposed to beams of accelerated heavy ions IV. Biophysical interpretation. Int J Radiat Biol 37:135–167

    Google Scholar 

  • Grosovsky AJ, deBoer JG, de Jong PJ, Drobetsky EA, Glickman BW (1988) Base substitutions, frameshifts, and small deletions constitute ionizing radiation-induced mutations in mammalian cells. Proc Natl Acad Sci USA 85:185–188

    Google Scholar 

  • Guerrero I, Villasante A, Corces V, Pellicer A (1984a) Activation of a c-K-ras oncogene by somatic mutation in mouse lymphomas induced by gamma radiation. Science 225:1159–1162

    Google Scholar 

  • Guerrero I, Calzada P, Mayer A, Pellicer A (1984b) A molecular approach to leukemogenesis: mouse lymphomas contain an activated c-ras oncogene. Proc Natl Acad Sci USA 81:202–205

    Google Scholar 

  • Hall EJ, Hei TK, Piao CQ (1989) Transformation by simulated radon daughter alpha particles; interaction with asbestos and modulation by tumor promotors. In: Chadwick KH, Seymour S, Barnhart B (eds) Cell transformation and radiation-induced cancer. Adam Hilger, New York, pp 293–299

    Google Scholar 

  • Hardwick JP, Schlenker RA, Huberman E (1989) Alteration of the c-mos locus in “normal” tissues from humans exposed to radium. Cancer Res 49:2668–2673

    Google Scholar 

  • Harris H (1988) The analysis of malignancy by cell fusion: the position in 1988. Cancer Res 48:3302- 3306

    Google Scholar 

  • Harris H, Klein G (1969) Malignancy of somatic cell hybrids. Nature 224:1314–1316

    Google Scholar 

  • He ZY, Piao CO, Waldren CA, Hei TK, Hall EJ (1990) Mutagenic potential of charged particles of defined LET. Poster presented at the 38th meeting of the Radiation Research Society, New Orleans

    Google Scholar 

  • Hei TK, Komatsu K, Hall EJ, Zaider M (1988a) Oncogenic transformation by charged particles of defined LET. Carcinogen 9:747–750

    Google Scholar 

  • Hei TK, Chen DJ, Brenner DJ, Hall EJ (1988b) Mutation induction by charged particles of defined linear transfer. Carcinogen 9:747–750

    Google Scholar 

  • Hieber L, Lücke-Huhle C (1983) PCC technique reveals severe chromatin lesions and repair in G2-arrested cells after alpha irradiation. Exp Cell Res 144:57–62

    Google Scholar 

  • Hieber L, Ponsel G, Roos H, Fenn S, Fromke E, Kellerer AM (1987) Absence of a dose-rate effect in the transformation of C3H 10T1/2 cells by a-particles. Int J Radiat Biol 52:859–869

    Google Scholar 

  • Holley WR, Chatterjee A (1990) Clustering of damage around a site of a radiation induced DNA strand break. Poster presented at the 38th annual meeting of the Radiation Research Society, New Orleans

    Google Scholar 

  • Holley WR, Chatterjee A, Magee JL (1990) Production of DNA strand breaks by direct effects of heavy charged particles. Radiat Res 121:161–168

    Google Scholar 

  • Iliakis G (1984) The mutagenicity of alpha particles in Ehrlich ascites tumor cells. Radiat Res 99:52–58

    Google Scholar 

  • Jaberaboansari A, Dunn WC, Preston RJ, Mitra S, Waters LC (1991) A comparative analysis of mutations induced by low and high LET radiation in a human shuttle plasmid. Radiat Res (in press)

    Google Scholar 

  • Jaffe DR, Bowden GT (1989) Detection of distinct transforming genes in X-ray induced tumors. Carcinogen 10:2243–2247

    Google Scholar 

  • Janowski M, Cox R, Strauss PG (1990) The molecular biology of radiation-induced carcinogenesis:thymic lymphoma, myeloid leukaemia and osteosarcoma. Int J Radiat Biol 57:677–691

    Google Scholar 

  • Jostes RF, Morgan TL, Gies RA, Fleck E, Gasper K, Cross FT (1990) Molecular analysis of radon-induced mutants. J Cell Biochem S14A:55

    Google Scholar 

  • Jostes RF, Fleck EW, Gies RH, Hui TE, Morgan TL, Schwartz JL, Wiencke JK, Cross FT (1991) Cytotoxic, clastogenic, and mutagenic response of mammalian cells exposed in vitro to radon and its progeny. In: Cross FT (ed) Indoor radon and lung cancer: reality or myth? 29th Hanford Symposium on Health and the Evnironment. Battelle Press, Richland, WA (in press)

    Google Scholar 

  • Kampf G, Eichhorn E (1983) DNA strand breakage by different radiation qualities and relations to cell killing: further results after the influence of a-particles and carbon ions. Stud Biophys 93:17–26

    Google Scholar 

  • Klinger HP, Kaelbling M (1986) Suppression of tumorigenicity in somatic cell hybrids. IV. Chromosomes of normal human cells associated with suppression of tumorigenicity in hybrids with D98AH2 carcinoma cells. Cytogenet Cell Genet 42:225–235

    Google Scholar 

  • Knudson AG Jr (1985) Hereditary cancer, oncogenes, and antioncogenes. Cancer Res 45:1437- 1443

    Google Scholar 

  • Krolewski B, Little JB (1989) Molecular analysis of DNA isolated from the different stages of X-ray-induced transformation in vitro. Mol Carcinogen 2:27–33

    Google Scholar 

  • Kronenberg A, Little JB (1989a) Locus specificity for mutation induction in human cells exposed to accelerated heavy ions. Int J Radiat Biol 55:913–924

    Google Scholar 

  • Kronenberg A, Little JB (1989b) Molecular characterization of thymidine kinase mutants of human cells induced by densely ionizing radiation. Mutat Res 211:215–224

    Google Scholar 

  • Lafuma J, Chmelevsky D, Chameaud J, Morin M, Masse R, Kellerer AM (1989) Lung carcinomas in Sprague-Dawley rats after exposure to low doses of radon daughters, fission neutrons, or y rays. Radiat Res 118:230–245

    Google Scholar 

  • Land H, Parada LF, Weinberg RA (1983) Tumorigenic conversion of primary embryo fibroblasts requires at least two cooperating oncogenes. Nature 304:596–602

    Google Scholar 

  • Leung FC, Saccomanno G (1988) Expression of epidermal growth-factor receptor and bombesin in archived paraffin-block uranium-miner lung tumors. In: Park JF, Pelroy RA (eds) Multilevel health effects research: from molecules to man. 27th Hanford Symposium on Health and Environment. Battelle Press, Richland, WA, pp 373–382

    Google Scholar 

  • Leung FC, Coleman JR, Dagle GE, Cross FT (1988) Involvement of growth factors and their receptors in radiation-induced carcinogenesis. In: Park JF, Pelroy RA (eds) Multilevel health effects research: from molecules to man. 27th Hanford Symposium on Health and Environment. Battelle Press, Richland, WA, pp 207–218

    Google Scholar 

  • Little JB, Kennedy AR, McGandy RB (1985) Effect of dose rate on the induction of experimental lung cancer in hamsters by a radiation. Radiat Res 103:293–299

    Google Scholar 

  • Lloyd EL, Gemmell MA, Henning CB, Gemmell DS, Zabransky BJ (1979) Transformation of mammalian cells by alpha particles. Int J Radiat Biol 36:467–478

    Google Scholar 

  • Lubin JH, Qiao Y-l, Taylor PR, Yao S-X, Schatzkin A, Mao B-L, Rao J-Y, Xuan X-Z, Li J-Y (1990) Quantitative evaluation of the radon and lung cancer association in a case control study of Chinese tin miners. Cancer Res 50:174–180

    Google Scholar 

  • Liicke-Huhle C (1982) Alpha-irradiation-induced G2 delay: a period of cell recovery. Radiat Res 89:298–308

    Google Scholar 

  • Liicke-Huhle C (1983) Endoreduplication in Chinese hamster cells during a-radiation induced G2 arrest. MutatRes 119:407–413

    Google Scholar 

  • Liicke-Huhle C, Herrlich P (1987) Alpha-radiation-induced amplification of integrated SV40 sequences is mediated by a trans-acting mechanism. Int J Cancer 39:94–98

    Google Scholar 

  • Liicke-Huhle C, Comper W, Hieber L, Pech M (1982) Comparative study of G2 delay and survival after americium-a and cobalt-y-irradiation. Radiat Environ Biophys 20:171–185

    Google Scholar 

  • Liicke-Huhle C, Pech M, Herrlich P (1986) Selective gene amplification in mammalian cells after exposure to Co y rays, 242Am a particles or uv light. Radiat Res 106:345–355

    Google Scholar 

  • Lutze LH, Winegar RA, Morgan WF, Cleaver JE, Jostes RF (1990) Detection of deletion mutations from X rays and radon alpha particles in human cells. Poster resented at the 38th annual meeting of the Radiation Research Society, New Orleans

    Google Scholar 

  • Mencl J, Jostes R, Cross F, Gies R, Bakale G, Rao P, Rerko R, Evans H (1989) Radon-induced mutation at an autosomal locus. Presented at the 37th annual meeting of the Radiation Research Society, Seattle

    Google Scholar 

  • Miles C, Meuth M (1989) DNA sequence determination of y-radiation-induced mutations of the hamster aprt locus. Mutat Res 227:97–102

    Google Scholar 

  • Mizuki K, Nose K, Okamoto H, Tsuchida N, Hayashi K (1985) Amplification of c-Kl-ras gene and aberrant expression of c-myc in WI-38 cells transformed in vitro by gamma irradiation. Biochem Biophys Res Commun 128:1037–1043

    Google Scholar 

  • Moolgavkar SH, Cross FT, Luebeck G, Dagle GE (1990) A two-mutation model for radon-induced lung tumors in rats. Radiat Res 121:28–37

    Google Scholar 

  • Mortimer R, Brustad T, Cormack DV (1965) Influence of linear energy transfer and oxygen tension on the effectiveness for induction of mutations and lethality in Saccharomyces cerevisiae. Radiat Res 26:465–482

    Google Scholar 

  • Munson RJ, Bridges BA (1973) The LET factor in mutagenesis by ionizing radiations I. Reversion to wild type of a bacteriophage T4 amber mutant. Int J Radiat Biol 24:257–273

    Google Scholar 

  • Nagasawa H, Cox AB, Lett JT (1980) The radiation responses of synchronous L5178Y S/S cells and their significance for radiobiological theory. Proc R Soc Lond B 211:25–49

    Google Scholar 

  • Nagasawa H, Robertson J, Little JB (1990a) Induction of chromosomal aberrations and sister chromatid exchanges by alpha particles in density-inhibited cultures of mouse 10T1/2 and 3T3 cells. Int J Radiat Biol 57:35–44

    Google Scholar 

  • Nagasawa H, Little JB, Inkret WC, Carpenter S, Thompson K, Raju MR, Chen DG, Strniste GF (1990b) Cytogenetic effects of extremely low doses of plutonium-238 alpha particle irradiation in CHO K-l cells. Mutat Res 244:233–238

    Google Scholar 

  • Nagasawa H, Little JB, Inkret WC, Carpenter S, Raju MR, Chen DJ, Strniste GF (1991) Response of X-ray sensitive CHO mutant cells to radiation II. Relationship between cell survival and the induction of chromosomal damage with low doses of alpha-particles. Radiat Res 126 (in press)

    Google Scholar 

  • Nero A, Schwehr MB, Nazaroff WW, Revzan KL (1986) Distribution of airborne radon-222 concentrations in U.S. homes. Science 234:992–997

    Google Scholar 

  • Newcombe EW, Steinberg JJ, Pellicer A (1988) ras oncogenes and phenotypic staging in N- methylnitrosourea- and y-irradiation-induced thymic lymphomas in C57BL/6J mice. Cancer Res 48:5514–5521

    Google Scholar 

  • Nowell P (1976) The clonal evolution of tumor cell populations. Science 194:23–28

    Google Scholar 

  • Nowell PC, Croce CM (1988) Chromosomal approaches to oncogenes and oncogenesis. FASEB J 2:3054–3060

    Google Scholar 

  • Ostashevsky JY (1990) Prediction of cell survival curves from DNA double-strand break repair data for low- and high-LET radiation. Int J Radiat Biol 57:523–536

    Google Scholar 

  • Petin VG, Kabakova NM (1981) RBE of densely ionizing radiation for wild-type and radiosensitive mutants of yeast. Mutat Res 82:285–294

    Google Scholar 

  • Pohl E, Pohl-Riiling J (1979) The dose-effect relationship of chromosome aberrations to a and y irradiation in a population subjected to an increased burden of natural radioactivity. Radiat Res 80:61–81

    Google Scholar 

  • Pohl-Riiling J, Fischer P (1983) Chromosome aberrations in inhabitants of areas with elevated natural radioactivity. In: Ishihara T, Sasaki MS (eds) Radiation-induced chromosome damage in man. Alan R Liss, New York, pp 527–560

    Google Scholar 

  • Pohl-Rüling J, Fischer P, Pohl E (1986) Effect on peripheral chromosomes. In: Hopke P (ed) Radon and its decay products. Proc Am Chem Soc, New York pp 419–429

    Google Scholar 

  • Prise KM, Davies S, Michael BD (1987) The relationship between radiation-induced DNA double- strand breaks and cell kill in hamster V79 fibroblasts irradiated with 250 kVp X-rays, 2.3 MeV neutrons or Pu a-particles. Int J Radiat Biol 52:893–902

    Google Scholar 

  • Prise KM, Davies S, Michael BD (1989) Non-linear dose-effect curve for DNA double-strand breaks by low LET radiation: the effect of eluting buffer composition on the measurement of breaks by the filter elution technique. Int J Radiat Biol 56:943–950

    Google Scholar 

  • Purrott RJ, Edwards AA, Lloyd DC, Stather JW (1980) The induction of chromosome aberrations in human lymphocytes by in vitro irradiation with a-particles from plutonium-239. Int J Radiat Biol 38:277–284

    Google Scholar 

  • Radford IR (1988) The dose-response for low-LET radiation-induced DNA double-strand breakage: methods of measurement and implications for radiation action models. Int J Radiat Biol 54:1–11

    Google Scholar 

  • Raju MR, Tobey RA, Jett JH, Walters RA (1975) Age response for line CHO Chinese hamster cells exposed to X-irradiation and alpha particles from plutonium. Radiat Res 63:422–433

    Google Scholar 

  • Raju MR, Frank JP, Bain E, Trujillo TT, Tobey RA (1977) Repair of potentially lethal damage in Chinese hamster cells after X and a irradiation. Radiat Res 71:614–621

    Google Scholar 

  • Raju MR, Eisen Y, Carpenter S, Inkret WC (1991) Radiobiology of a particles. Ill Cell inactivation vs. a particle passages through the cell nucleus. Radiat Res (in press)

    Google Scholar 

  • Rassoulzadegan M, Cowie A, Carr A, Glaichenhaus N, Kamen R, Cuzin F (1982) The roles of individual Polyomavirus early proteins in oncogenic transformation. Nature 300:125–226

    Google Scholar 

  • Reddy NMS, Rao BS, Murthy MSS (1976) Liquid holding recovery in stationary and log phase cultures of diploid yeast exposed to gamma and alpha radiations. Radiat Environ Biophys 13:167–175

    Google Scholar 

  • Ritter MA, Cleaver JE, Tobias CA (1977) High-LET radiations induce a large proportion of non-rejoin- ing DNA breaks. Nature 266:653–655

    Google Scholar 

  • Roberts CJ, Goodhead DT (1987) The effect of Pu a-particles on the mouse fibroblast cell line C3H 10T1/2: characterization of source and RBE for survival. Int J Radiat Biol 52:871–882

    Google Scholar 

  • Robertson JB, Koehler A, George J, Little JB (1983) Oncogenic transformation of mouse BALB/3T3 cells by plutonium-238 alpha particles. Radiat Res 96:261–274

    Google Scholar 

  • Roots R, Yang TC, Craise L, Blakely EA, Tobias CA (1979) Impaired repair capacity of DNA breaks induced in mammalian cellular DNA by accelerated heavy ions. Radiat Res 78:38–49

    Google Scholar 

  • Roots R, Chatterjee A, Chang P, Lommel L, Blakely EA (1985) Characterization of hydroxyl radical-induced damage after sparsely and densely ionizing irradiation. Int J Radiat Biol 47:157–166

    Google Scholar 

  • Ruley HE (1983) Adenovirus early region 1A enables viral and cellular transforming genes to transform primary cells in culture. Nature 304:603–606

    Google Scholar 

  • Samet JM (1989) Radon and lung cancer. J Natl Cancer Inst 81:745–756

    Google Scholar 

  • Samet JM, Pathak DR, Morgan MV, Marbury MC, Key CR, Valdivia A A (1989) Radon progeny exposure and lung cancer risk in New Mexico U miners: a case-control study. Health Phys 56:415–121

    Google Scholar 

  • Sasaki H (1984) Cell killing and division delay in asynchronous and synchronized HeLa cells irradiated with alpha particles or X rays. Radiat Res 99:311–323

    Google Scholar 

  • Sasaki H (1989) Expression of potentially lethal damage in cultured mammalian cells irradiated with or X-rays. Sci Pap Inst Phys Chem Res 83:13–16

    Google Scholar 

  • Sawey MJ, Kennedy AR (1990) Radiation-induced activation of the c-myc oncogene and a novel transforming gene in mouse C3H10T1/2 cells. J Cell Biochem 14A:83

    Google Scholar 

  • Saxon PJ, Srivatsan ES, Stanbridge EJ (1986) Introduction of human chromosome 11 via microcell transfer controls tumorigenic expression of HeLa cells. EMBO J 5:3461–3466

    Google Scholar 

  • Schaaper RM, Danforth BN, Glickman BW (1986) Mechanisms of spontaneous mutagenesis: an analysis of the spectrum of spontaneous mutation in the E. coli lac I gene. J Mol Biol 189:273–284

    Google Scholar 

  • Schwartz J, Shadley JF, Atcher RW, Tang J, Whitlock J, Rotmensch J (1990) Comparison of radon- daughter-induced effects in repair-proficient and repair-deficient cell lines. Environ Mol Mutagen 16:178–184

    Google Scholar 

  • Seemayer TA, Cavene WK (1989) Molecular mechanisms of oncogenesis. Lab Invest 60:585–599

    Google Scholar 

  • Seidman MM, Dixon K, Razzaque A, Zagursky RJ, Berman ML (1985) A shuttle vector plasmid for studying carcinogen-induced point mutations in mammalian cells. Gene 38:233–237

    Google Scholar 

  • Shadley JD, Whitlock JL, Rotmensch J, Atcher RW, Tang J, Schwartz JL (1991) The effects of radon daughter alpha-particle irradiation in K1 and xrs-5 CHO cell lines. Mutat Res (in press)

    Google Scholar 

  • Sinclair WK (1968) Cyclic X-ray responses in mammalian cells in vitro. Radiat Res 33:620–643

    Google Scholar 

  • Sipki MO, Denette ER, Lurie AG (1990) Determination of gamma ray induced mutations in normal and repair deficient cells using a shuttle vector system. J Cell Biochem S14A:56

    Google Scholar 

  • Sorrentino V, Drozdoff V, Zeitz L, Fleissner E (1987) Increased radiation-induced transformation in C3H/10T1/2 cells after transfer of an exogenous c-myc gene. Proc Natl Acad Sci USA 84:4131- 4134

    Google Scholar 

  • Sparkes RS, Murphree AL, Lingua RW, Sparkes MC, Field LL, Funderburk SJ, Benedict WF (1983) Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage analysis to esterase D. Science 219:971–973

    Google Scholar 

  • Suzuki M, Watanabe M, Suzuki K, Nakano K, Kaneko I (1989) Neoplastic cell transformation by heavy ions. Radiat Res 120:468–476

    Google Scholar 

  • Temin HM (1988) Evolution of cancer genes as a mutation-driven process. Cancer Res 48:1697–1701

    Google Scholar 

  • Terasima T, Tolmach LJ (1961) Changes in X-ray sensitivity of HeLa cells during the division cycle. Nature 190:1210–1211

    Google Scholar 

  • Thacker J (1986) The nature of mutants induced by ionising radiation in cultured cells III. Molecular characterization of HPRT-deficient mutants induced by y-rays or a-particles showing that the majority have deletions of all or part of the hprt gene. Mutat Res 160:267–275

    Google Scholar 

  • Thacker J, Stretch A (1985) Responses of 4 X-ray-sensitive CHO cell mutants to different radiations and to irradiation conditions promoting cellular recovery. Mutat Res 146:99–108

    Google Scholar 

  • Thacker J, Stretch A, Stephens MA (1979) Mutation and inactivation of cultured mammalian cells exposed to beams of accelerated heavy ions. II. Chinese hamster V79 cells. Int J Radiat Biol 36:137–148

    Google Scholar 

  • Thacker J, Stretch A, Goodhead DT (1982) The mutagenicity of a particles from plutonium-238. Radiat Res 92:343–352

    Google Scholar 

  • Thomassen DG, Sieler FA, Shyr L-J, Griffith WC (1990a) Alpha-particles induce preneoplastic transformation of rat tracheal epithelial cells in culture. Int J Radiat Biol 57:395–405

    Google Scholar 

  • Thomassen DG, Newton GJ, Guilmette RA (1990b) Transforming potency of inhaled radon progeny for rat tracheal epithelial cells. Proc Am Assoc Cancer Res 31:109

    Google Scholar 

  • Thraves P, Salehi Z, Dritschilo A, Rhim JS (1990) Neoplastic transformation of immortalized human epidermal keratinocytes by ionizing radiation. Proc Natl Acad Sci USA 87:1174–1177

    Google Scholar 

  • Ueno AM, Goldin EM, Cox AB, Lett JT (1979) Deficient repair and degradation of DNA in X-irradiated L5178Y S/S cells: cell-cycle and temperature dependence. Radiat Res 79:377–389

    Google Scholar 

  • van Heyningen V, Boyd PA, Seawright A, Fletcher JM, Fantes JA, Buckton KE, Spowart G, Porteous DJ, Hill RE, Newton MS, Hastie ND (1985) Molecular analysis of chromosome 11 deletions in anridia Wilms tumor syndrome. Proc Natl Acad Sci USA 82:8592–8596

    Google Scholar 

  • Vulpis N (1973) Chromosome aberrations induced in human peripheral blood lymphocytes using heavy particles from B (n, a) reaction. Mutat Res 18:103–111

    Google Scholar 

  • Ward JF (1985) Biochemistry of DNA lesions. Radiat Res 104:S 103-S111

    Google Scholar 

  • Weinberg RA (1989) Oncogenes, antioncogenes, and the molecular bases of multistep carcinogenesis. Cancer Res 49:3713–3721

    Google Scholar 

  • Weissman BE, Saxon PJ, Pasquale SR, Jones GR, Geiser AG, Stanbridge EJ (1987) Introduction of a normal human chromosome 11 into a Wilms’ tumor cell line controls its tumorigenic expression. Science 236:175–180

    Google Scholar 

  • Whaley JM, Little JB (1990) Molecular characterization of hprt mutants induced by low- and high-LET radiations in human cells. Mutat Res 243:35–45

    Google Scholar 

  • Whitmore GF, Varghese AJ, Gulyas S (1989) Cell cycle responses of two X-ray sensitive mutants defective in DNA repair. Int J Radiat Biol 56:657–665

    Google Scholar 

  • Wlodek D, Hittelman WN (1987) The repair of double-strand DNA breaks correlates with radiosensitivity of L5178Y-S and L5178Y-R cells. Radiat Res 112:146–155

    Google Scholar 

  • Yang TC, Craise LM, Mei MT, Tobias CA (1985) Neoplastic cell transformation by heavy charged particles. Radiat Res 104:S177-S187

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1991 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Evans, H.H. (1991). Cellular and Molecular Effects of Radon and Other Alpha Particle Emitters. In: Obe, G. (eds) Advances in Mutagenesis Research. Advances in Mutagenesis Research, vol 3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76232-1_2

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-76232-1_2

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-76234-5

  • Online ISBN: 978-3-642-76232-1

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics