Free Access
Issue
Med Sci (Paris)
Volume 19, Number 11, Novembre 2003
Page(s) 1128 - 1136
Section M/S Revues
DOI https://doi.org/10.1051/medsci/200319111128
Published online 15 November 2003
  1. Viallard JF, Lacombe F, Belloc F, Pellegrin JL, Reiffers J. Mécanismes moléculaires contrôlant le cycle cellulaire: aspects fondamentaux et implications en oncologogie. Cancer Radiother 2001; 5: 109–29. [Google Scholar]
  2. Thuret JY, Mann C. Kinases activatrices de la division cellulaire: in vivo veritas ? Med Sci 1998; 14: 215–8. [Google Scholar]
  3. Hulleman E, Boonstra J. Regulation of G1 phase progression by growth factors and the extracellular matrix. Cell Mol Life Sci 2001; 58: 80- 93. [Google Scholar]
  4. Fishman DD, Segal S, Livneh E. The role of protein kinase C in G1 and G2/M phases of the cell cycle. Int J Oncol 1998; 12: 181–6. [Google Scholar]
  5. Jayadev S, Liu B, Bielawska AE, et al. Role for ceramide in cell cycle arrest. J Biol Chem 1995; 270: 2047–52. [Google Scholar]
  6. Pearce AK, Humphrey TC. Integrating stress-response and cell-cycle checkpoint pathways. Trends Cell Biol 2001; 11: 426–33. [Google Scholar]
  7. Takenaka K, Moriguchi T, Nishida E. Activation of the protein kinase p38 in the spindle assembly checkpoint and mitotic arrest. Science 1998; 280: 599–602. [Google Scholar]
  8. De Rycke J, Oswald E. Cytolethal distending toxin (CDT): a bacterial weapon to control host cell proliferation ? FEMS Microbiol Lett 2001; 203: 141–8. [Google Scholar]
  9. Comayras C, Tasca C, Peres SY, Ducommun B, Oswald E, De Rycke J. Escherichia coli cytolethal distending toxin blocks the HeLa cell cycle at the G2/M transition by preventing cdc2 protein kinase dephosphorylation and activation. Infect Immun 1997; 65: 5088–95. [Google Scholar]
  10. Sert V, Cans C, Tasca C, et al. The bacterial cytolethal distending toxin (CDT) triggers a G2 cell cycle checkpoint in mammalian cells without preliminary induction of DNA strand breaks. Oncogene 1999; 18: 6296–304. [Google Scholar]
  11. Escalas N, Davezac N, De Rycke J, Baldin V, Mazars R, Ducommun B. Study of the cytolethal distending toxin-induced cell cycle arrest in HeLa cells: involvement of the CDC25 phosphatase. Exp Cell Res 2000; 257: 206–12. [Google Scholar]
  12. Cortes-Bratti X, Karlsson C, Lagergard T, Thelestam M, Frisan T. The Haemophilus ducreyi cytolethal distending toxin induces cell cycle arrest and apoptosis via the DNA damage checkpoint pathways. J Biol Chem 2001; 276: 5296–302. [Google Scholar]
  13. Alby F, Mazars R, De Rycke J, et al. Study of the cytolethal distending toxin (CDT)-activated cell cycle checkpoint. Involvement of the CHK2 kinase. FEBS Lett 2001; 491: 261–5. [Google Scholar]
  14. Li L, Sharipo A, Chaves- Olarte E, et al. The Haemophilus ducreyi cytolethal distending toxin activates sensors of DNA damage and repair complexes in proliferating and non-proliferating cells. Cell Microbiol 2002; 4: 87–99. [Google Scholar]
  15. Sugai M, Kawamoto T, Peres SY, et al. The cell cyclespecific growth-inhibitory factor produced by Actinobacillus actinomycetemcomitans is a cytolethal distending toxin. Infect Immun 1998; 66: 5008–19. [Google Scholar]
  16. Peres SY, Marches O, Daigle F, et al. A new cytolethal distending toxin (CDT) from Escherichia coli producing CNF2 blocks HeLa cell division in G2/M phase. Mol Microbiol 1997; 24: 1095–107. [Google Scholar]
  17. Pickett CL, Cottle DL, Pesci EC, Bikah G. Cloning, sequencing, and expression of the Escherichia coli cytolethal distending toxin genes. Infect Immun 1994; 62: 1046–51. [Google Scholar]
  18. Scott DA, Kaper JB. Cloning and sequencing of the genes encoding Escherichia coli cytolethal distending toxin. Infect Immun 1994; 62: 244–51. [Google Scholar]
  19. Lewis DA, Stevens MK, Latimer JL, et al. Characterization of Haemophilus ducreyi cdtA, cdtB, and cdtC mutants in in vitro and in vivo systems. Infect Immun 2001; 69: 5626–34. [Google Scholar]
  20. Lara-Tejero M, Galan JE. CdtA, CdtB, and CdtC form a tripartite complex that is required for cytolethal distending toxin activity. Infect Immun 2001; 69: 4358–65. [Google Scholar]
  21. Frisk A, Lebens M, Johansson C, et al. The role of different protein components from the Haemophilus ducreyi cytolethal distending toxin in the generation of cell toxicity. Microb Pathog 2001; 30: 313–24. [Google Scholar]
  22. Deng K, Latimer JL, Lewis DA, Hansen EJ. Investigation of the interaction among the components of the cytolethal distending toxin of Haemophilus ducreyi. Biochem Biophys Res Commun 2001; 285: 609–15. [Google Scholar]
  23. Lara-Tejero M, Galan JE. A bacterial toxin that controls cell cycle progression as a deoxyribonuclease I-like protein. Science 2000; 290: 354–7. [Google Scholar]
  24. Elwell CA, Dreyfus LA. DNase I homologous residues in CdtB are critical for cytolethal distending toxin-mediated cell cycle arrest. Mol Microbiol 2000; 37: 952–63. [Google Scholar]
  25. Elwell C, Chao K, Patel K, Dreyfus L. Escherichia coli CdtB mediates cytolethal distending toxin cell cycle arrest. Infect Immun 2001; 69: 3418–22. [Google Scholar]
  26. Hassane DC, Lee RB, Mendenhall MD, Pickett CL. Cytolethal distending toxin demonstrates genotoxic activity in a yeast model. Infect Immun 2001; 69: 5752–9. [Google Scholar]
  27. Okuda J, Fukumoto M, Takeda Y, Nishibuchi M. Examination of diarrheagenicity of cytolethal distending toxin: suckling mouse response to the products of the cdtABC genes of Shigella dysenteriae. Infect Immun 1997; 65: 428–33. [Google Scholar]
  28. Purdy D, Buswell CM, Hodgson AE, McAlpine K, Henderson I, Leach SA. Characterisation of cytolethal distending toxin (CDT) mutants of Campylobacter jejuni. J Med Microbiol 2000; 49: 473–9. [Google Scholar]
  29. Stevens MK, Latimer JL, Lumbley SR, et al. Characterization of a Haemophilus ducreyi mutant deficient in expression of cytolethal distending toxin. Infect Immun 1999; 67: 3900–8. [Google Scholar]
  30. Young RS, Fortney KR, Gelfanova V, et al. Expression of cytolethal distending toxin and hemolysin is not required for pustule formation by Haemophilus ducreyi in human volunteers. Infect Immun 2001; 69: 1938–42. [Google Scholar]
  31. Barth H, Klingler M, Aktories K, Kinzel V. Clostridium botulinum C2 toxin delays entry into mitosis and activation of p34cdc2 kinase and cdc25- C phosphatase in HeLa cells. Infect Immun 1999; 67: 5083–90. [Google Scholar]
  32. Nougayrede JP, Marches O, Boury M, et al. The longterm cytoskeletal rearrangement induced by rabbit enteropathogenic Escherichia coli is Esp dependent but intimin independent. Mol Microbiol 1999; 31: 19–30. [Google Scholar]
  33. Demuth DR, Savary R, Golub E, Shenker BJ. Identification and analysis of fipA, a Fusobacterium nucleatum immunosuppressive factor gene. Infect Immun 1996; 64: 1335–41. [Google Scholar]
  34. Shenker BJ, Datar S. Fusobacterium nucleatum inhibits human T-cell activation by arresting cells in the mid-G1 phase of the cell cycle. Infect Immun 1995; 63: 4830–6. [Google Scholar]
  35. Yoshida J, Ishibashi T, Nishio M. Growth-inhibitory effect of a streptococcal antitumor glycoprotein on human epidermoid carcinoma A431 cells: involvement of dephosphorylation of epidermal growth factor receptor. Cancer Res 2001; 61: 6151–7. [Google Scholar]
  36. Gutkind JS. The pathways connecting G proteincoupled receptors to the nucleus through divergent mitogen-activated protein kinase cascades. J Biol Chem 1998; 273: 1839–42. [Google Scholar]
  37. Yoshida J, Takamura S, Nishio M. Characterization of a streptococcal antitumor glycoprotein (SAGP). Life Sci 1998; 62: 1043–53. [Google Scholar]
  38. Pitari GM, Di Guglielmo MD, Park J, Schulz S, Waldman SA. Guanylyl cyclase C agonists regulate progression through the cell cycle of human colon carcinoma cells. Proc Natl Acad Sci USA 2001; 98: 7846–51. [Google Scholar]
  39. Van Setten PA, van Hinsbergh VW, Van den Heuvel LP, et al. Verocytotoxin inhibits mitogenesis and protein synthesis in purified human glomerular mesangial cells without affecting cell viability: evidence for two distinct mechanisms. J Am Soc Nephrol 1997; 8: 1877–88. [Google Scholar]
  40. Klapproth JM, Scaletsky IC, McNamara BP, et al. A large toxin from pathogenic Escherichia coli strains that nhibits lymphocyte activation. Infect Immun 2000; 68: 2148–55. [Google Scholar]
  41. Matsui K, Nagano K, Arai T, Hirono I, Aoki T. DNA sequencing of the gene encoding Salmonella typhimurium-derived T-cell inhibitor (STI) and characterization of the gene product, cloned STI. FEMS Immunol Med Microbiol 1998; 22: 341–9. [Google Scholar]
  42. Knipp U, Birkholz S, Kaup W, Opferkuch W. Partial characterization of a cell proliferation-inhibiting protein produced by Helicobacter pylori. Infect Immun 1996; 64: 3491–6. [Google Scholar]
  43. Shenker BJ, Vitale L, Slots J. Immunosuppressive effects of Prevotella intermedia on in vitro human lymphocyte activation. Infect Immun 1991; 59: 4583–9. [Google Scholar]
  44. Grana X, Reddy EP. Cell cycle control in mammalian cells: role of cyclins, cyclin dependent kinases (CDKs), growth suppressor genes and cyclin-dependent kinase inhibitors (CKIs). Oncogene 1995; 11: 211–9. [Google Scholar]
  45. Elledge SJ. Cell cycle checkpoints: preventing an identity crisis. Science 1996; 274: 1664–72. [Google Scholar]
  46. Zhou BB, Elledge SJ. The DNA damage response: putting checkpoints in perspective. Nature 2000; 408: 433–9. [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.