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British Journal of Cancer logoLink to British Journal of Cancer
. 1983 Dec;48(6):809–817. doi: 10.1038/bjc.1983.271

Inhibition of cell-cycle progression by acute treatment with various degrees of hypoxia: modifications induced by low concentrations of misonidazole present during hypoxia.

E O Pettersen, T Lindmo
PMCID: PMC2011554  PMID: 6652020

Abstract

The effect on cell-cycle progression in various phases of the cell cycle caused by an acute exposure to hypoxia in absence and presence of misonidazole (MISO) was investigated. Exponentially growing and synchronized cells of the human line NHIK 3025 were exposed to different degrees of hypoxia for a short period (1.5 or 3 h). The cell-cycle progression was studied both during and after hypoxia by flow-cytometric recording of DNA-histograms from treated and untreated cells. The rate of cell-cycle progression was reduced during hypoxia only if the O2-concentration was below 1000 ppm. The inhibition was phase specific with a strong effect in S (reduced DNA-synthesis), and a specific cell-cycle inhibition in late G1, probably at the G1/S-border. For cells inhibited (or arrested for extreme hypoxia) at the G1/S-border, the cell-cycle progression changed back to normal shortly after aerobic conditions were re-established. For cells rendered hypoxic and inhibited during S, hypoxia exerted a lasting effect expressed by a low cell-cycle progression rate even after aerobic conditions were re-established. This effect was strongly dependent on both the degree and the duration of the hypoxic treatment. The presence of a low concentration of MISO (0.05 mM) during hypoxia did not affect the cell-cycle progression during hypoxia at any O2-concentration. For cells rendered hypoxic during S, however, MISO (0.05 mM) counteracted the lasting effect of hypoxia for all concentrations of O2 where this lasting effect was observed.

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Selected References

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  1. Anderson E. C., Petersen D. F., Tobey R. A. Biochemical balance and syncronized cell cultures. Nature. 1967 Sep 2;215(5105):1083–1084. doi: 10.1038/2151083a0. [DOI] [PubMed] [Google Scholar]
  2. Bedford J. S., Mitchell J. B. The effect of hypoxia on the growth and radiation response of mammalian cells in culture. Br J Radiol. 1974 Oct;47(562):687–696. doi: 10.1259/0007-1285-47-562-687. [DOI] [PubMed] [Google Scholar]
  3. Boag J. W. Cell respiration as a function of oxygen tension. Int J Radiat Biol Relat Stud Phys Chem Med. 1970;18(5):475–478. doi: 10.1080/09553007014551361. [DOI] [PubMed] [Google Scholar]
  4. Born R., Hug O., Trott K. R. The effect of prolonged hypoxia on growth and viability of Chinese hamster cells. Int J Radiat Oncol Biol Phys. 1976 Jul-Aug;1(7-8):687–697. doi: 10.1016/0360-3016(76)90151-6. [DOI] [PubMed] [Google Scholar]
  5. Brock W. A., Swartzendruber D. E., Grdina D. J. Kinetic heterogeneity in density-separated murine fibrosarcoma subpopulations. Cancer Res. 1982 Dec;42(12):4999–5003. [PubMed] [Google Scholar]
  6. Crissman H. A., Tobey R. A. Cell-cycle analysis in 20 minutes. Science. 1974 Jun 21;184(4143):1297–1298. doi: 10.1126/science.184.4143.1297. [DOI] [PubMed] [Google Scholar]
  7. FROESE G. The respiration of ascites tumour cells at low oxygen concentrations. Biochim Biophys Acta. 1962 Mar 12;57:509–519. doi: 10.1016/0006-3002(62)91158-7. [DOI] [PubMed] [Google Scholar]
  8. Hahn G. M., Bagshaw M. A. Serum concentration: effects on cycle and x-ray sensitivity of mammalian cells. Science. 1966 Jan 28;151(3709):459–461. doi: 10.1126/science.151.3709.459. [DOI] [PubMed] [Google Scholar]
  9. Hall E. J., Roizin-Towle L. Hypoxic sensitizers: radiobiological studies at the cellular level. Radiology. 1975 Nov;117(2):453–457. doi: 10.1148/117.2.453. [DOI] [PubMed] [Google Scholar]
  10. Koch C. J., Kruuv J., Frey H. E., Snyder R. A. Plateau phase in growth induced by hypoxia. Int J Radiat Biol Relat Stud Phys Chem Med. 1973 Jan;23(1):67–74. doi: 10.1080/09553007314550061. [DOI] [PubMed] [Google Scholar]
  11. Lindmo T., Pettersen E. O. Delay of cell cycle progression after X-irradiation of synchronized populations of human cells (NHIK 3025) in culture. Cell Tissue Kinet. 1979 Jan;12(1):43–57. doi: 10.1111/j.1365-2184.1979.tb00112.x. [DOI] [PubMed] [Google Scholar]
  12. Lindmo T., Pettersen E. O., Wibe E. Cell-cycle inhibition by misonidazole of human cells cultivated in vitro under aerobic conditions. Br J Cancer. 1979 Nov;40(5):755–760. doi: 10.1038/bjc.1979.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Lindmo T., Steen H. B. Flow cytometric measurement of the polarization of fluorescence from intracellular fluorescein in mammalian cells. Biophys J. 1977 May;18(2):173–187. doi: 10.1016/S0006-3495(77)85606-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Lovhaug D., Wibe E., Oftebro R., Pettersen E. O., Brustad T. Recovery from x-ray induced damage in human cells grown in culture. Neoplasma. 1977;24(5):513–520. [PubMed] [Google Scholar]
  15. Olivotto M., Paoletti F. The role of respiration in tumor cell transition from the noncycling to the cycling state. J Cell Physiol. 1981 May;107(2):243–249. doi: 10.1002/jcp.1041070210. [DOI] [PubMed] [Google Scholar]
  16. PUCK T. T., CIECIURA S. J., FISHER H. W. Clonal growth in vitro of human cells with fibroblastic morphology; comparison of growth and genetic characteristics of single epithelioid and fibroblast-like cells from a variety of human organs. J Exp Med. 1957 Jul 1;106(1):145–158. doi: 10.1084/jem.106.1.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Pettersen E. O., Bakke O., Lindmo T., Oftebro R. Cell cycle characteristics of synchronized and asynchronous populations of human cells and effect of cooling of selected mitotic cells. Cell Tissue Kinet. 1977 Nov;10(6):511–522. doi: 10.1111/j.1365-2184.1977.tb00309.x. [DOI] [PubMed] [Google Scholar]
  18. Pettersen E. O., Christensen T., Bakke O., Oftebro R. A change in the oxygen effect throughout the cell-cycle of human cells of the line NHIK 3025 cultivated in vitro. Int J Radiat Biol Relat Stud Phys Chem Med. 1977 Feb;31(2):171–184. doi: 10.1080/09553007714550191. [DOI] [PubMed] [Google Scholar]
  19. Pettersen E. O., Lindmo T. Low concentrations of misonidazole counteract effects of extreme hypoxia on cells in S. Br J Cancer. 1981 Mar;43(3):355–366. doi: 10.1038/bjc.1981.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Pettersen E. O., Nome O., Rønning O. W., Oftebro R. Effects of benzaldehyde on survival and cell-cycle kinetics of human cells cultivated in vitro. Eur J Cancer Clin Oncol. 1983 Apr;19(4):507–514. doi: 10.1016/0277-5379(83)90114-1. [DOI] [PubMed] [Google Scholar]
  21. Pettersen E. O., Oftebro R., Brustad T. X-ray inactivation of human cells in tissue culture under aerobic and extremely hypoxic conditions in the presence and absence of TMPN. Int J Radiat Biol Relat Stud Phys Chem Med. 1973 Sep;24(3):285–296. doi: 10.1080/09553007314551121. [DOI] [PubMed] [Google Scholar]
  22. Sinclair W. K. Cyclic x-ray responses in mammalian cells in vitro. Radiat Res. 1968 Mar;33(3):620–643. [PubMed] [Google Scholar]
  23. Stratford I. J., Adams G. E. Effect of hyperthermia on differential cytotoxicity of a hypoxic cell radiosensitizer, Ro-07-0582, on mammalian cells in vitro. Br J Cancer. 1977 Mar;35(3):307–313. doi: 10.1038/bjc.1977.44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. TERASIMA T., TOLMACH L. J. Variations in several responses of HeLa cells to x-irradiation during the division cycle. Biophys J. 1963 Jan;3:11–33. doi: 10.1016/s0006-3495(63)86801-0. [DOI] [PMC free article] [PubMed] [Google Scholar]

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