L5178Y sublines: a look back from 40 years. Part 2: Response to ionizing radiation

References

• Alexander P, Mikulski ZB. 1961. Mouse lymphoma cells with different radiosensitivities. Nature 192: 572–573.
   PubMed Web of Science ®Google Scholar
• Beer JZ, Budzicka E, Niepokojczycka E, Rosiek 0, Szumiel I, Walicka M. 1983. Loss of tumorigenicity with simultaneous changes in radiosensitivity and photosensitivity during in vitro growth of L5178Y murine lymphoma cells. Cancer Research 43, 4736–4742.
   Google Scholar
• Beer JZ, Jacobson ED, Evans HH, Szumiel I. 1984. X-ray and UV mutagenesis in two L5178Y cell strains differing in tumor-igenicity, radiosensitivity, and DNA repair. British Journal of Cancer Suppl. 6: 107–111.
   PubMedGoogle Scholar
• Beer JZ, Lett JT, Alexander P. 1963. Influence of temperature and medium on the X-ray sensitivities of leukemia cells in vitro. Nature 199: 193–194.
   PubMed Web of Science ®Google Scholar
• Beer JZ, Mend J, Horng MF, Gregg EC, Evans HH. 1985. Effects of low dose-rate (0.003-0.025 Gy/h) chronic X-irradiation on radioresistant and radiosensitive L5178Y mouse lymphoma cells. International Journal of Radiation Biology 48: 609–619.
   Google Scholar
• Beer JZ, Szumiel I, Walicka M. 1973. Cross-sensitivities to X-rays and UV-light of two strains of murine lymphoma L5178Y cells in vitro. Bulletin de l'Academie Polonaise des Sciences (serie des sciences biologiques) 21: 837–840.
   Google Scholar
• Block WD, Yu YP, Merlde D, Gifford JL, Ding Q, Meek K, Lees-Miller SP. 2004. Autophosphorylation-dependent remodeling of the DNA-dependent protein kinase catalytic subunit regulates ligation of DNA ends. Nucleic Acid Research 32: 4351–4357.
   PubMed Web of Science ®Google Scholar
• Boothman DA, Fukunaga N, Wang M. 1994. Down-regulation of topoisomerase I in mammalian cells following ionizing radia-tion. Cancer Research 54: 4618–4626.
   PubMed Web of Science ®Google Scholar
• Bouiyk E, Gradzka I, Iwaneriko T, Kruszewski M, Sochanowicz B, Szumiel I. 2000. The response of L5178Y lymphoma sublines to oxidative stress: antioxidant defence, iron content and nuclear translocation of the p65 subunit of NF-KB. Acta Biochimica Polonica 47: 881–888.
   PubMed Web of Science ®Google Scholar
• Buraczewska I, Gasinska A, Gradzka I, Jarocewicz N, Sochano-wicz B, Szumiel I. 1999. Erbstatin-induced increase in apoptosis does not radiosensitize L5178Y cells. Nuldeonika 44: 561–578.
   Google Scholar
• Elia MC, Bradley MO. 1992. Influence of chromatin structure on the induction of DNA double strand breaks by ionizing radiation. Cancer Research 52: 1580–1586.
   PubMed Web of Science ®Google Scholar
• Endlich B, Radford IR, Forrester HB, Dewey WC. 2000. Computerized video time-lapse microscopy studies of ionizing radiation-induced rapid-interphase and mitosis-related apop-tosis in lymphoid cells. Radiation Research 153: 36–48.
   PubMed Web of Science ®Google Scholar
• Evans HH, Horng MF. 1988. The repair of potentially lethal damage and sublethal damage in strains of mouse L5178Y lymphoma cells differing in radiation sensitivity. Radiation Research 113: 183–190.
   PubMed Web of Science ®Google Scholar
• Evans HH, Horng MF, Mend J, Glazier KG, Beer JZ. 1985. The influence of dose-rate on the lethal and mutagenic effects of X-rays in proliferating L5178Y cells differing in radiation sensitivity. International Journal of Radiation Biology 47: 553–562.
   Web of Science ®Google Scholar
• Evans HH, Mend 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. Proceedings of the National Academy of Sciences, USA 83: 4379–4383.
   PubMed Web of Science ®Google Scholar
• Evans HH, Ricanati M, Horng MF. 1987. Deficiency in DNA repair in mouse lymphoma strain L5178Y-S. Proceedings of the National Academy of Sciences, USA 84: 7562–7566.
   PubMed Web of Science ®Google Scholar
• Finnie NJ, Gottlieb TM, Blunt T, Jeggo PA, Jackson SP. 1995. DNA-dependent kinase activity is absent in xrs6 cells: implications for site-specific recombination and DNA double strand repair. Proceedings of the National Academy of Sciences, USA 92: 320–324.
   PubMed Web of Science ®Google Scholar
• Glaser KB, Sung A, Bauer J, Weichman BM. 1993. Regulation of eicosanoid biosynthesis in the macrophage. Involvement of protein tyrosine phosphorylation and modulation by selective protein tyrosine kinase inhibitors. Biochemical Pharmacology 45: 711–721.
   Google Scholar
• Gradzka I, Buraczewska I, Kuduk-Jaworska J, Romaniewska A, Szumiel I. 2003. Radiosensitizing properties of novel hydro-xydicarboxylato platinum(II) complexes with high or low reactivity with thiols: two modes of action. Chemico-Biological Interactions 146: 165–177.
   Google Scholar
• Gradzka I, Skierski J, Szumiel I. 1998. DNA repair, cell cycle progression and cell death following camptothecin treatment in two murine lymphoma L5178Y sublines. Cell Biochemistry and Function 16: 239–252.
   PubMed Web of Science ®Google Scholar
• Jaworska A, Szumiel I, De Angelis P, Olsen G, Reitan J. 2001. Evaluation of ionizing radiation sensitivity markers in a panel of lymphoid cell lines. International Journal of Radiation Biology 77: 269–280.
   PubMed Web of Science ®Google Scholar
• Johanson KJ, Sundell-Bergman S, Szumiel I, Wlodek D. 1985. Effects of irradiation and inhibition of adenosine diphosphate ribosyl transferase in radiation sensitive and resistant mouse lymphoma (L5178Y) cells. Acta Radiologica Oncologica 24: 451–457.
   Web of Science ®Google Scholar
• Johanson KJ, Wlodek D, Szumiel I. 1982. DNA repair and replication in radiation-sensitive and -resistant mouse lympho-ma cells gamma-irradiated under aerobic and hypoxic conditions. International Journal of Radiation Biology 41: 261–270.
   Web of Science ®Google Scholar
• Kapiszewska M, Lange CS. 1988. The effects of reduced temperature and/or starvation conditions on the radiosensitiv-ity and repair of potentially lethal damage and sublethal damage in L5178Y-R and L5178Y-S cells. Radiation Research 113: 458–472.
   PubMed Web of Science ®Google Scholar
• Kapiszewska M, Lange CS. 1989. The effect of hypothermic treatment on the repair or expression of X-ray damage measured in split dose experiments on L5178Y-S cells. Radiation and Environmental Biophysics 28: 303–317.
   PubMed Web of Science ®Google Scholar
• Kharbanda S, Pandey P, Jin S, Inoue S, Bharti A, Yuan Z, Weichselbaum RR, Weaver D, Kufe D. 1997. Functional interaction between DNA-PK and c-Abl in response to DNA damage. Nature 386: 732–735.
   PubMed Web of Science ®Google Scholar
• Kleczkowska HE, Szumiel I. 1990. Histone acceptors for ADP-ribose in UVC or gamma-irradiated L5178Y sublines differing in DNA repair abilities. Nukleonika 35: 213–226.
   Google Scholar
• Kleczkowska HE, Malanga M, Szumiel I, Althaus FR. 2002. Poly ADP-ribosylation in two L5178Y murine lymphoma sublines differentially sensitive to DNA-damaging agents. International Journal of Radiation Biology 78: 527–534.
   PubMed Web of Science ®Google Scholar
• Kruszewski M, Green MHL, Lowe JE, Szumiel I. 1994. DNA strand breakage, cy-totoxicity and mutagenicity of hydrogen peroxide treatment at 4°C and 37°C in L5178Y sublines. Mutation Research 308: 233–241.
   PubMedGoogle Scholar
• Kruszewski M, Green MHL, Lowe JE, Szumiel I. 1995. Comparison of effect of iron and calcium chelators on the response of L5178Y sublines to x-rays and H202. Mutation Research 326: 155–163.
   PubMed Web of Science ®Google Scholar
• Kruszewski M, Iwanefiko T. 1998. Induction of DNA breakage in X-irradiated nucleoids selectively stripped of nuclear proteins in two mouse lymphoma cell lines differing in radiosensitivity. Acta Biochimica Polonica 45: 701–704.
   PubMed Web of Science ®Google Scholar
• Kruszewski M, Iwanefiko T. 2003. Labile iron pool correlates with iron content in the nucleus and the formation of oxidative DNA damage in mouse lymphoma L5178Y cell lines. Acta Biochimica Polonica 50: 211–215.
   PubMed Web of Science ®Google Scholar
• Kruszewski M, Iwanenko T, Bouzyk E, Szumiel I. 1999. Chelating of iron and copper alters properties of DNA in L5178Y cells, as revealed by the comet assay. Mutation Research 434: 53–60.
   PubMedGoogle Scholar
• Kruszewski M, Ovodkov N, Gerasimenko VN, Karpovski AL, Rosiek 0, Sawicki Z. 1988. The influence of radiation quality on survival of two mouse lymphoma L5178Y cell strains of different radiation sensitivity. 2. Effects of 9 GeV protons. Nukleonika 33: 339–343.
   Google Scholar
• Kruszewski M, Ovodkov JV, Krasavin EA, Lobachevsky PN, Rosiek 0, Sawicki Z, Tcherevatenko AP. 1989a. The influence of radiation quality on survival of two mouse lymphoma L5178Y cell strains of different radiation sensitivity. 2. Effects of 2.5 MeV helium ions. Nukleonika 34: 110–114.
   Google Scholar
• Kruszewski M, Ovodkov JV, Krasavin EA, Lobachevsky PN, Rosiek 0, Sawicki Z, Tcherevatenko AP. 1989b. The influence of radiation quality on survival of two mouse lymphoma L5178Y cell strains of different radiation sensitivity. 2. Effects of 1.6 MeV deuterons. Nukleonika 34: 315–321.
   Google Scholar
• Kruszewski M, Wojewodzka M, Iwanenko T, Szumiel I, Okuyama A. 1998. Differential inhibitory effect of OK-1035 on DNA repair in L5178Y murine lymphoma sublines with functional or defective repair of double strand breaks. Mutation Research 409: 31–36.
   PubMed Web of Science ®Google Scholar
• Kruszewski M, Zastawny TH, Szumiel I. 2001. Repair of gamma-ray-induced base damage in L5178Y sublines is damage type-dependent and unrelated to radiation sensitivity. Acta Biochi-mica Polonica 48: 525–533.
   PubMed Web of Science ®Google Scholar
• Lees-Miller SP, Meek K. 2003. Repair of DNA double strand breaks by non-homologous end joining. Biochimie 85: 1161–1173.
   PubMed Web of Science ®Google Scholar
• Lipinski P, Drapier JC, Oliveira L, Retmanska H, Sochanowicz B, Kruszewski M. 2000. Intracellular iron status as a hallmark of mammalian cell susceptibility to oxidative stress: a study of L5178Y mouse lymphoma cell lines differentially sensitive to H202. Blood 95: 2960–2966.
   PubMed Web of Science ®Google Scholar
• Ljungman M. 1991. The influence of chromatin structure on the frequency of radiation-induced DNA strand breaks: a study using nuclear and nucleoid monolayers. Radiation Research 126: 58–64.
   PubMed Web of Science ®Google Scholar
• Ljungman M, Nyberg S, Nygren J, Eriksson M, Ahnstrom G. 1991. DNA-bound proteins contribute much more than soluble intracellular compounds to the intrinsic protection against radiation-induced DNA strand breaks in human cells. Radiation Research 127: 171–176.
   PubMed Web of Science ®Google Scholar
• Neshat MS, Raitano AB, Wang HG, Reed JC, Sawyers CL. 2000. The survival function of the Bcr-Abl oncogene is mediated by Bad-dependent and -independent pathways: roles for phos-phatidylinositol 3-kinase and Raf. Molecular and Cell Biology 20: 1179–1186.
   Web of Science ®Google Scholar
• Okada S. 1970. Formation of giant cells. In: Altman KI, Gerber GB, Okada S, editors. Radiation biochemistry, Vol. 1: Cells. New York: Academic Press; 1970. p. 239–246.
   Google Scholar
• Okui T, Endoh D, Kon Y, Hayashi M. 2002. Deficiency in nuclear accumulation of G22p1 and Xrcc5 proteins in hyper-radiosensitive Long-Evans Cinnamon (LEC) rat cells after X irradiation. Radiation Research 157: 553–561.
   PubMed Web of Science ®Google Scholar
• Olive PL, Banath JP. 1995. Radiation-induced DNA double-strand breaks produced in histone-depleted tumor cell nuclei measured using the neutral comet assay. Radiation Research 142: 144–152.
   PubMed Web of Science ®Google Scholar
• Pfeiffer P, Goedecke W, Kuhfittig-Kulle S, Obe G. 2004. Pathways of DNA double-strand break repair and their impact on the prevention and formation of chromosomal aberrations. Cytogenetics and Genome Research 104: 7–13.
   PubMed Web of Science ®Google Scholar
• Radford IR. 1994. p53 status, DNA double-strand break repair proficiency, and radiation response of mouse lymphoid and myeloid cell lines. International Journal of Radiation Biology 66: 557–560.
   PubMed Web of Science ®Google Scholar
• Radford IR. 2002a. DNA lesion complexity and induction of apoptosis by ionizing radiation. International Journal of Radiation Biology 78: 457–466.
   PubMed Web of Science ®Google Scholar
• Radford IR. 2002b. Transcription-based model for the induction of interchromosomal exchange events by ionizing irradiation in mammalian cell lines that undergo necrosis. International Journal of Radiation Biology 78: 1081–1093.
   PubMed Web of Science ®Google Scholar
• Sato K, Chen DJ, Eguchi-Kasai K, Itsukaichi H, Odaka T, Strniste GF. 1995. Interspecific complementation between mouse and Chinese hamster cell mutants hypersensitive to ionizing radiation. Journal of Radiation Research 36: 38–45.
   PubMed Web of Science ®Google Scholar
• Sato K, Ito A, Shiomi T, Hama-Inaba H, Ishikawa H, Yoshizumi T, Nakazawa T. 1986. X-ray-sensitive mutants of mouse mammary carcinoma cells are hypersensitive to bleomycin and hydrogen peroxide. Japanese Journal of Cancer Research 77: 456–461.
   PubMedGoogle Scholar
• Sochanowicz B, Szumiel I. 1996. Arachidonic acid metabolism in murine lymphoma cell sublines differing in radiation sensitiv-ity. Prostaglandins, Leukotriens and Essential Fatty Acids 55: 241–247.
   PubMed Web of Science ®Google Scholar
• Sochanowicz B, Szumiel I. 2001. Cytoplasmic activity of tyrosine kinase protein, c-Abl, in L5178Y murine lymphoma sublines - a link to differential apoptosis proneness? Institute of Nuclear Chemistry and Technology Annual Report 2000: 104–105.
   Google Scholar
• Stiff T, Shtivelman E, Jeggo P, Kysela B. 2004. AHNAK interacts with the DNA ligase IV- XRCC4 complex and stimulates DNA ligase IV-mediated double-stranded ligation. DNA Repair 3: 245–256.
   PubMed Web of Science ®Google Scholar
• Storer RD, Kranyak AR, Mckelvey TW, Elia HC, Goodrow TL, Deluca JG. 1997. The mouse lymphoma L5178Y TK + /- cell line is heterozygous for a codon 170 mutation in the p53 tumor suppressor gene. Mutation Research 373: 157–165.
   PubMed Web of Science ®Google Scholar
• Suzuki A, Ito T, Kawano H, Hayashida M, Hayasaki Y, Tsutomi Y, Akahane K, Nakano T, Miura M, Shiraki K. 2000. Survivin initiates procaspase 3/p21 complex formation as a result of interaction with Cdk4 to resist Fas-mediated cell death. Oncogene 19: 1346–1353.
   PubMed Web of Science ®Google Scholar
• Szumiel I. 1978. Requirements for potentiation of radiation effect by a platinum complex. International Journal of Radiation Biology 33: 605–608.
   Web of Science ®Google Scholar
• Szumiel I. 1979. Response of two strains of L5178Y cells to cis-dichlorobis (cyclopentylamine) platinum (II). I. Cross-sensi-tivity to cis-PAD and UV light. Chemico-Biological Interactions 24: 51–72.
   PubMed Web of Science ®Google Scholar
• Szumiel I, Budzicka E, Niepokojczycka E, Wlodek D, Beer JZ. 1981. The response of L5178Y-R and L5178Y-S cells to X rays under oxic and hypoxic conditions. Radiation Research 87: 592–601.
   PubMed Web of Science ®Google Scholar
• Szumiel I, Buraczewska I, Gradzka I, Gasiriska A. 1995. Effects of topoisomerase I-targeted drugs on radiation response of L5178Y sublines differentially radiation and drug sensitive. International Journal of Radiation Biology 67: 441–448.
   PubMed Web of Science ®Google Scholar
• Szumiel I, Jaworska A, Kapiszewska M, John A, Gradzka I, Sochanowicz B. 2000. Differential induction of apoptosis in x-irradiated L5178Y sublines bearing p53 mutation. Radiation and Environmental Biophysics 39: 33–40.
   PubMed Web of Science ®Google Scholar
• Szumiel I, Kapiszewska M, John A, Gradzka I, Kowalczyk D, Janik P. 2001. Caffeine-inhibitable control of the radiation-induced G2 arrest in L5178Y-S cells deficient in non-homologous end-joining. Radiation and Environmental Biophysics 40: 137–143.
   PubMed Web of Science ®Google Scholar
• Szumiel I, Walicka M, Budzicka E, Beer JZ. 1978. Susceptibility of L5178Y-R and L5178Y-S cells to HTO, 3H-lysine and 3H-thymidine exposure. Current Topics in Radiation Research Quarterly 12: 157–167.
   PubMedGoogle Scholar
• Szumiel I, Wlodek D, Johanson KJ. 1988. Differential effect of benzamide on NAD+ content and the frequency of chromatid aberrations in X-irradiated L5178Y-R and L5178Y-S cells. Acta Oncologica 27: 851–855.
   PubMed Web of Science ®Google Scholar
• Szumiel I, Wlodek D, Johnson KJ, Sundell-Bergman S. 1984b. ADP-ribosylation and post-irradiation cellular recovery in two strains of L5178Y cells. British Journal of Cancer, Suppl. 6, 33–38.
   Google Scholar
• Szumiel I, Wlodek D, Lustyik G. 1984a. Ion content and the response of L5178Y-R and L5178Y-S cells to X rays and ionophore A23187. Radiation and Environmental Biophysics 23: 255–267.
   PubMed Web of Science ®Google Scholar
• Tauchi H, Sawada S. 1994. Analysis of mitotic cell death caused by radiation in mouse leukaemia L5178Y cells: apoptosis is the ultimate form of cell death following mitotic failure. Interna-tional Journal of Radiation Biology 65: 449–455.
   PubMed Web of Science ®Google Scholar
• Van Buul PP, Van Duyn-Goedhart A, Sankaranarayanan K. 1999. In vivo and in vitro radioprotective effects of the prostaglandin El analogue misoprostol in DNA repair-proficient and - deficient rodent cell systems. Radiation Research 152: 398–403.
   PubMed Web of Science ®Google Scholar
• Walicka M, Koerner IJ. 1982. Lethal effects and DNA break rejoining in two L5178Y cell lines irradiated with fast neutrons and x-rays. Studia Biophysica 87: 47–56.
   Google Scholar
• Walicka M, Koerner IJ, Malz W. 1979. Survival and DNA single strand break rejoining in L5178Y-R and L5178Y-S cells after neutron irradiation. Studia Biophysica 76: 49–50.
   Google Scholar
• Wlodek D, Hittelman WN. 1987. The repair of double strand breaks correlates with radiosensitivity of L5178Y-S and L5178Y-R cells. Radiation Research 112: 146–155.
   PubMed Web of Science ®Google Scholar
• Wlodek D, Hittelman WN. 1988a. The relationship of DNA and chromosome damage to survival of synchronized X-irradiated L5178Y cells. I. Initial damage. Radiation Research 115: 550 — 565.
   Google Scholar
• Wlodek D, Hittelman WN. 1988b. The relationship of DNA and chromosome damage to survival of synchronized X-irradiated L5178Y cells. II. Repair. Radiation Research 115: 566–575.
   PubMed Web of Science ®Google Scholar
• Wlodek D, Olive PL. 1992. Neutral filter elution detects differences in chromatin organization which can influence cellular radiosensitivity. Radiation Research 132: 242–247.
   PubMed Web of Science ®Google Scholar
• Wojewódzka M, Kruszewski M, Sochanowicz B, Szumiel I. 2004. Differential DNA double strand break fixation dependence on poly(ADP-ribosylation) in L5178Y and CHO cells, Interna-tional Journal of Radiation Biology 80: 473–482.
   PubMed Web of Science ®Google Scholar
• Yau TM, Kim SC, Gregg EC, Nygaard OF. 1979. Inverse X-irradiation split-dose effect in a murine lymphoma cell line. International Journal of Radiation Biology 35: 577–581.
   Web of Science ®Google Scholar
• Zastawny TH, Kruszewski M, Olinski R 1998. Ionizing radiation and hydrogen peroxide-induced oxidative DNA base damage in two L5178Y cell lines. Free Radicals in Biology and Medicine 24: 1250–1255.
   PubMed Web of Science ®Google Scholar