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Induction of apoptosis by the marine sponge (Mycale) metabolites, mycalamide A and pateamine

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Abstract

The marine sponge metabolites mycalamide A (myca-lamide) and pateamine are extremely cytotoxic. While mycalamide has been shown to inhibit protein synthesis, the mechanism by which these compounds induce cell death is unknown. Using DNA laddering, Annexin-V staining, and morphological analysis, we demonstrate that both metabolites induce apoptosis in several different cell lines. Furthermore, both mycalamide and pateamine were more potent inducers of apoptosis in the 32D myeloid cell line after transformation with either the ras or bcr-abl oncogenes. This increased sensitivity was also observed in response to the protein synthesis inhibitors cycloheximide and puromycin, and cytosine-β-D-arabinofurano-side (Ara-C), an inducer of DNA damage. We propose, therefore, that in 32D cells where Ras signalling has been altered either by constitutive expression of oncogenic ras or by Bcr/abl-mediated perturbation of upstream signalling events, increased susceptibility to apoptosis by a range of stimuli is conferred.

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References

  1. Perry N, Blunt J, Munro M. Mycalamide A, an antiviral compound from a New Zealand sponge of the genus Mycale. J Am Chem Soc 1988; 110: 4850-4851.

    Google Scholar 

  2. Northcote P, Blunt J, Munro M. Pateamine: A potent cytotoxin from the New Zealand marine sponge, Mycale Sp. Tetrahedron Letters 1991; 32: 6411-6414.

    Google Scholar 

  3. Perry N, Blunt J, Munro M, Thompson A. Antiviral and antitumor agents from a New Zealand sponge, Mycale sp. 2. Structures and solution conformation of mycalamides A and B. J Org Chem 1990; 55: 223-227.

    Google Scholar 

  4. Romo D, Rzasa R, Shea H, et al. Total synthesis and immunosuppressive activity of (-)-Pateamine A and related compounds: implementation of a ?-lactam-based macrocyclization. J Am Chem Soc 1998; 120: 12237-12254.

    Google Scholar 

  5. Galvin F, Freeman G, Razi-Wolf Z, Benacerraf B, Nadler L, Reiser H. Effects of cyclosporin A, FK506, and mycalamide A on the activation of murine CD4+ T cells by the murine B7 antigen. Eur J Immunol 1993; 23: 283-286.

    Google Scholar 

  6. Burres N, Clement J. Antitumor activity and mechanism of action of the novel marine natural products mycalamide-A and-B and onnamide. Cancer Res 1989; 49: 2935-2940.

    Google Scholar 

  7. West L, Northcote P, Hood K, Miller J, Page M. Mycalamide D, a new cytotoxic amide from the New Zealand marine sponge Mycale sp. J Natural Products 2000; 63: 707-709.

    Google Scholar 

  8. Simpson J, Garson M, Blunt J, Munro M, Hooper J. Mycalamides C and D, cytotoxic compounds from the marine sponge Stylinos n. Species. J Natural Products 2000; 63: 704-706.

    Google Scholar 

  9. Richter A, Kocienski P, Raubo P, Davies D. The in vitro biological acitivities of synthetic 18-O-methyl mycalamide B, 10-epi-18-O-methyl mycalamide B and pederin. Anti-Cancer Drug Design 1997; 12: 217-227.

    Google Scholar 

  10. Raff M. Cell suicide for beginners. Nature 1998; 396: 119-123.

    Google Scholar 

  11. Rivera S, Guillot S, Aggassandian C, Ben A, Khrestchatisky M. Serum deprivation-induced apoptosis in cultured hippocampi is prevented by kainate. Neuroreport 1998; 9: 3949-3953.

    Google Scholar 

  12. Tang D, Lahti J, Grenet J, Kidd V. Cycloheximide-induced T-cell death is mediated by a fas-associated death domaindependent mechanism. J Biol Chem 1999; 274: 7245-7252.

    Google Scholar 

  13. Gulbins E, Coggeshall K, Brenner B, Schlottmann K, Linderkamp O, Lang F. Fas-induced apoptosis is mediated by activation of a ras and rac protein-regulated signaling pathway. J Biol Chem 1996: 271: 26389-26394.

    Google Scholar 

  14. Downward J. Ras signalling and apoptosis. Curr Opin Genetics and Development 1998; 8: 49-54.

    Google Scholar 

  15. Ahmed N, Anderson S, Berridge M. IL-3 induces apoptosis in a ras-transformed myeloid cell line. Apoptosis 1999; 4: 71-80.

    Google Scholar 

  16. Liu H, Chen C, Lee C, Chou Y. Selective activation of oncogenic Ha-ras-induced apoptosis in NIH/3T3 cells. Brit J Cancer 1998; 77: 1777-1786.

    Google Scholar 

  17. Gallagher A, Burnett A, Bowen D, Darley R. Mutant RAS selectively promote sensitivity of myeloid leukemia cells to apoptosis by a protein kinase C-dependent process. Cancer Res 1998; 58: 2029-2035.

    Google Scholar 

  18. Cortez D, Stoica G, Pierce J, Prendergast A. The BCR/ABL tyrosine kinase inhibits apoptosis by activating a ras-dependent signalling pathway. Oncogene 1996; 13: 2589-2594.

    Google Scholar 

  19. Ogawara H, Kigashi K, Uchino K, Perry N. Change of rastransformed NRK-cells back to normal morphology by mycalamides A and B, antitumor agents from a marine sponge. Chem Pharm Bull 1991; 39: 2152-2154.

    Google Scholar 

  20. Valtieri M, Tweardy D, Caracciolo D. Cytokine-dependent granulocytic differentation. J Immunol 1987; 138: 3829-3835.

    Google Scholar 

  21. McWhirter J, Wang J. An actin-binding function contributes to transformation by the Bcr-abl oncoprotein of Philadelphia chromosome-positive human leukemias. EMBO J 1993; 12: 1533-1546.

    Google Scholar 

  22. Darzynkiewicz Z, Li X. Measurement of cell death by flow cytometry. In: Cotter T, Martin S ed. Techniques in Apoptosis: A User's Guide. 1st edn. UK: Portland Press 1997: 71-106.

    Google Scholar 

  23. Gorman A, McCarthy J, Finucane D, Reville W, Cotter T. Morphological assessment of apoptosis. In: Cotter T, Martin S ed. Techniques in Apoptosis: A User's Guide. 1st edn. UK: Portland Press 1997: 1-20.

    Google Scholar 

  24. Berridge M, Tan A, McCoy K, Wang R. The biochemical and cellular basis of cell proliferation assays that use tetrazolium salts. Biochemica 1996; 4: 14-19.

    Google Scholar 

  25. Yang G, Liao J, Kim K, Yurkow E, Yang C. Inhibition of growth and induction of apoptosis in human cancer cell lines by tea polyphenols. Carinogenesis 1998; 19: 611-616.

    Google Scholar 

  26. Meijerman I, Blom W, de Bont H, Mulder G, Nagelkerke J. Induction of apoptosis and changes in nuclear G-actin are mediated by different pathways: The effect of inhibitors of protein and RNA synthesis is isolated rat hepatocytes. Toxicol App Pharm 1999; 156: 46-55.

    Google Scholar 

  27. Lewis J, Adams D, Fa S. Selective sensitivity of macrophages to cytotoxicity by inhibitors of macromolecular synthesis: Induction of apoptosis. J Leukocyte Biology 1995; 57: 635-642.

    Google Scholar 

  28. Chen C, Liou J, Forman L, Faller D. Differential regulation discrete apoptotic pathways by ras. J Biol Chem 1998; 273: 16700-16709.

    Google Scholar 

  29. Leverrier Y, Thomas J, Perkins G, Mangeney M, Collins M, Marvel J. In bone marrow derived Baf-3 cells, inhibition of apoptosis by IL-3 is mediated by two independent pathways. Oncogene 1997; 14:425-430.

    Google Scholar 

  30. Kinoshita T, Yokota T, Arai K, Miyajima A, et al. Suppression of apoptotic death in hematopoietic cells by signalling through the IL-3/GMCSF receptors. EMBO J 1995; 14: 266-275.

    Google Scholar 

  31. Chi S, Kitanaka C, Noguchi K, et al. Oncogenic ras triggers cell suicide through the activation of a caspase-independent cell death program i human cancer cells. Oncogene 1999. 18: 2281-2290.

    Google Scholar 

  32. Ohira T, Nishio K, Kanzawa F, et al. Hypersensitivity of NIH3T3 cells transformed by H-ras gene to DNAtopoisomerase-1 inhibitors. Int J Cancer 1996; 67: 702-708.

    Google Scholar 

  33. Chan T, Chang C, Koonchanok M, Geahlen R. Selective inhibition of the growth of ras-transformed human bronchial epithelial cells by emodin, a protein-tyrosine kinase inhibitor. Biochem Biophys Res Comm 1993; 193: 1152-1158.

    Google Scholar 

  34. Hall-Jackson C, Jones T, Eccles N, et al. Induction of cell death by stimulation of proten kinase C in human epithelial cells expressing a mutant ras oncogene: A potential therapeutic target. Br J Cancer 1998; 78: 641-651.

    Google Scholar 

  35. Gulbins E, Brenner B, Schlottman K, et al. Fas-induced programmed cell death is mediated by a ras-regulated O2-synthesis. Immunol 1996; 89: 205-212.

    Google Scholar 

  36. Gishizky M. Molecular mechanism of bcr/abl-induced oncogenesis. Cytokines Mol Therapy 1996; 2: 251-261.

    Google Scholar 

  37. McGahon A, Nishioka W, Martin S, Mahboubi A, Cotter T, Green D. Regulation of the apoptotic cell death pathway by abl. J Biol Chem 1995; 270:22625-22631.

    Google Scholar 

  38. Koo H, Monks A, Mikheev A, et al. Enhanced sensitivity to 1-beta-D-arabinofuranosylcytosine and topoisomerase II inhibitors in tumor cell lines harboring activated ras oncogenes. Cancer Res 1996; 56: 5211-5216.

    Google Scholar 

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Hood, K.A., West, L.M., Northcote, P.T. et al. Induction of apoptosis by the marine sponge (Mycale) metabolites, mycalamide A and pateamine. Apoptosis 6, 207–219 (2001). https://doi.org/10.1023/A:1011340827558

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  • DOI: https://doi.org/10.1023/A:1011340827558

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