Abstract
Prostatic Cancer is the leading site for cancer in men over 50 years of age and is the second leading cause of cancer deaths in the US (1). Clinically manifest prostatic cancer is more common in the US than in Japan while the incidence of latent cancer is similar between the two countries. The incidence of prostatic cancer of first generation males of Japanese living in the US is the same as that of US males. The implication is that life style differences are important for the progression of the disease. As prostatic cancer is refractory to most standard chemotherapeutic agents and hormone therapy is only palliative it may be that it will be easier to prevent the progression of prostatic cancer than to cure it. Consideration should be given to 3 omega unsaturated fatty acids, which are common in fish oils, as possible agents in a study of prevention of progression. The 3 omega unsaturated fatty acids have proven beneficial in the prevention of cancer and reduced the growth of prostatic cancer in nude mice (2,3). Other cultural differences in nutrition such as the use of green tea should be investigated to identify other potential anti-tumor progression factors.
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References
Silverburg, E., and Lubera, J.A. Cancer Statistics, CA 39:3–22, 1989.
Telang, N.T., Basu, A., Kurihara, H., Osborne, M.P. and Modak, M.J. Modulation in the expression of murine mammary tumor virus, ras proto-oncogene and of alveolar hyperplasia by fatty acids in mouse mammary explant cultures. Anticancer Res., 8:971–976, 1988.
Karmali, R.A., Reichel, P., Cohen, L.A., Terano, T., Hirai, A., Tamura, Y. and Yoshida, S. The effects of dietary omega-3 fatty acids on the DU-145 transplantable human prostatic tumor. Anticancer Res., 7:1173–1180, 1987.
Raina, A., Pajula, R., Eloranta, T. A rapid assay for spermidine and spermine synthesis: distribution of polyamine synthesizing enzymes and methionine adenosyltransferase in rat tissues. FEBS Lett., 76:252–256, 1976.
Pegg, A.E., Lockwood, D.H. and Williams-Ashman, H.G. Concentrations of polyamines and their enzymic synthesis during androgen-induced prostatic growth. Biochem. J., 117:17–31, 1970.
Heston, W.D.W., Kadmon, D. and Fair, W.R Copenhagen rat prostatic tumor ornithine decarboxylase activity (ODC) and the effect of the ODC inhibitor α-DFMO. The Prostate, 3:383–389, 1982.
Tabor, C.W. and Tabor, H. Polyamines. Ann. Rev. Biochem., 53:740–790, 1984.
Pegg, A.E. Polyamine metabolism and its importance in neoplastic growth and as a target for chemotherapy. Cancer Res., 48:759–774, 1988.
Porter, C.W. and Sufrin, J.R Interference with polyamine biosynthesis and/or function by analogs of polyamines or methionine as a potential chemotherapeutic strategy. Anticancer Res., 6:535–535, 1986.
Seppanen P., Alhonen-Hongisto, L. and Janne, J. Death of tumor cells in response to the use of a stimulated polyamine uptake for the transport of MGBG. Eur. J. Biochem., 18:571–576, 1981.
Herr, H.W., Kleinert, E.L., Relyea, N.M. and Whitmore, W.F. Jr. Potentiation of MGBG by DFMO in rat prostate. Cancer, 53:1294–1296, 1984.
Romijin, J.C., Van Steenbruge, G.J. and Schroeder, F.H. Effects of polyamine antimetabolites in the growth rate of human prostatic tumors transplantable into nude mice. Fouth int. workshop on immune deficient animals. (Karger, Basel) pp. 370, 1984.
Persson, L., Holm, I., Asle, A. and Heby, O. Curative effect of DFMO on mice bearing mutant L1210 leukemia cells deficient in polyamine uptake. Cancer Res., 48:4807–4811, 1988.
Kadmon, D. and Heston, W.D.W. Manuscript in preparation.
Heston, W.D.W., Kadmon, D., Covey, D.F. and Fair, W.R Differential effect of DFMO on the in vivo uptake of 14C-labeled polyamines and MGBG by a prostate derived tumor. Cancer Res., 44:1034–1040, 1984.
Heston, W.D.W., Yang, C-R., Pliner, L., Russo, P. and Covey, D.F. Cytotoxic activity of a polyamine analog, monoaziridinyl putrescine, against the PC-3 human prostatic carcinoma cell line. Cancer Res., 47:3627–3631, 1987.
Welch, M.J., Coleman, R.E., Straatman, M.G., Asberry, B.E., Primeau, J.L., Fair, W.R. and Ter-Pergossian, M.-M. C11-labeled methylated polyamine analogs: uptake in prostate and tumor in animal models. J. Nuel. Med., 18:74–78, 1977.
Kadmon, D., Welsh, M.J., and personal communication.
Bergeron, R.J. Methods for the selective modification of spermidine and its homologs. Acc. Chem. Res., 19:105–113, 1986.
Bergeron, R.J., Hawthorne, T.R., Vinson, J.R.T., Beck, D.F. Jr. and Igeno, M.J. Role of the methylene backbone in the antiproliferative activity of polyamine analogs on L1210 cells. Cancer Res., 49:2959–2964, 1989.
Schuber, F. Influence of polyamines on membrane functions. Biochem. J., 260:1–10, 1989.
Marton, L.J. Effects of treatment with DNA-directed cancer chemotherapeutic agents after polyamine depletion. Pharmacol. Ther., 32:183–190, 1987.
Scher, H., Yagoda, A., Ahmed, T., et al. Phase II trial of mitoguazone in patients with hormone resistant adenocarcinoma of the prostate. J. Clin. Oncol., 3:224–229, 1989.
Story, M.T., Sassa, J., Jacobs, S.C. and Lawson, R.K Prostatic growth factor: purification and structural relationship to basic fibroblast growth factor. Biochem., 26:3843–3849, 1987.
Matuo, Y., Nishi, N. and Wada, F. Growth factors in the prostate. Arch. Androl., 19:193–210, 1987.
Matuo, Y., Nishi Matsui, S., Sandberg, A.A., Issacs, J.T. and Wada, F. Heparin binding affinity of rat prostatic growth factor in normal and cancerous prostates: partial purification and characterization of rat prostatic growth factor in the Dunning tumor. Cancer Res., 47:188–192, 1987.
Mannson, P.F., Adams, P., Kan, M. and McKeehan W.L. Heparin-binding growth factor gene expression and receptor characteristics in normal rat prostate and two transplantable rat prostate tumors. Cancer Res., 49:1485–1494, 1989.
Mydlo, J.H., Bulbul, M.A., Richon, V.M., Heston, W.D.W. and Fair, W.R. Heparin-binding growth factor isolated from human prostatic extracts. The Prostate, 12:343–355, 1988.
Mydlo, J.H., Michaeli, J., Heston, W.D.W. and Fair, W.R. Expression of basic fibroblast growth factor mRNA in BPH and prostatic carcinoma. The Prostate, 13:241–247, 1988.
Smith, E.P., Russell, W.E., French, F.S. and Wilson, E.M. A form of basic FGF is secreted into the adluminal fluid of the rat coagulating gland (anterior prostate). The Prostate, 14:353–365, 1989.
Nishi, N., Matuo, Y., Kuritomi, K., Takenaka, I., Usami, M., Kotake, T. and Wada, F: Comparative analysis of growth factors in normal and pathologic human prostates. The Prostate, 13:39–48, 1988.
Coffey, R.J., Leoff, E.B., Shipley, G.D, and Moses, H.L. Suramin inhibition of growth factor binding and mitogenicity in AKR-2B cells. J. Cell. Physiol., 132:143–148, 1987.
Stein, C.A., LaRocca, R.V., McAtee, T.R. and Myers, C.E. Suramin an anticancer drug with a unique mechanism of action. J. Clin. Oncol., 7:499–508, 1989.
Myers, C.E. Presentation at MSKCC.
Finch, P.W., Rubin, J.S., Miki T., Ron, D. and Aaronson, S.A. Human KGF is FGF-related with properties of a paracrine effector of epithelial cell growth. Science, 245:752–755, 1989.
Chang, S-M. and Chung, L.W.K Interaction between prostatic fibroblast and epithelial cells in culture: Role of androgen. Endocrinol., 125:2719–2727, 1989.
Chackal-Roy, M., Niemeyer, C., Moore, M. and Zetter, B.R. Stimulation human prostatic carcinoma cell growth by factors present in human bone marrow. J. Clin. Invest., 84:43–50, 1989.
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Heston, W.D.W. (1991). Growth Factor Antagonists in Prostatic Cancer: Suramin and Cytotoxic Polyamines as Potential Therapy. In: Karr, J.P., Coffey, D.S., Smith, R.G., Tindall, D.J. (eds) Molecular and Cellular Biology of Prostate Cancer. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3704-5_15
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DOI: https://doi.org/10.1007/978-1-4615-3704-5_15
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