Timed Daily Administration of Prolactin and Corticosteroid Hormone Reduces Murine Tumor Growth and Enhances Immune Reactivity

Reference

• Bartsch C, Bartsch H, Fluchter S H. Evidence for modulation of melatonin secretion in men with benign and malignant tumors of the prostate: relationship with the pituitary hormones. J Pineal Res. 1985; 2: 121–32
   PubMed Web of Science ®Google Scholar
• Bartsch C, Bartsch H, Fuchs U. Stage-dependent depression of melatonin in patients with primary breast cancer. Correlation with prolactin, thyroid stimulating hormone, and steroid receptors. Cancer. 1989; 64: 426–33
   PubMed Web of Science ®Google Scholar
• Bemton E, Bryant H, Holaday J. Prolactin and prolactin secretagogues reverse immunosuppression in mice treated with cysteamine, glucocorticoids or cyclosporin-A. Brain Behav Immunol. 1992; 6: 394–408
   PubMedGoogle Scholar
• Bernton E W, Meltzer M S, Holaday J W. Suppression of macrophage activation and T-lymphocyte function in hypoprolactinemic mice. Science 1988; 239: 401–4
   PubMed Web of Science ®Google Scholar
• Born J, Lange T, Hansen K. Effects of sleep and circadian rhythm on human circulating immune cells. J Immunol. 1997; 158: 4454–64
   PubMed Web of Science ®Google Scholar
• Brainard G C, Knobler R L, Podolin P L. Neuroimmunology: modulation of the hamster immune system by photoperiod. Life Sci. 1987; 40: 1319–26
   PubMedGoogle Scholar
• Brock M A. Seasonal rhythmicity in lymphocyte blastogenic response of mice persists in a constant environment. J Immunol. 1983; 130: 2686
   Google Scholar
• Bureau J P, Coupe M, Labreoque C. Chronopharmacological study of the effect of corticosterone on BGC-induced granulocyte migration in normal and in adrenalec-tomized mice. Chronopharmacology. 1986; 3: 309–12
   Google Scholar
• Bureau J P, Garrelly L, Coupe M. Circadian rhythm studies on BGC-induced migration of PMN in normal and adrenalectomized mice. Chronopharmacology. 1984; 1: 333–36
   Google Scholar
• Chadwick D J, Ackrill K. Circadian clocks and their adjustment. Ciba Foundation Symposium 183. John Wiley and Sons., ChichesterU.K. 1995
   Google Scholar
• Cincotta A H, Knisely T L, Landry R J. The immunoregulatory effects of prolactin in mice are time of day dependent. Endocrinology. 1995; 136: 2163–71
   PubMedGoogle Scholar
• Cincotta A H, Schiller B C, Landry R J. Circadian neuroendocrine role in agerelated changes in body fat stores and insulin sensitivity of the male Sprague-Dawley rat. Chronobiol Int. 1993; 10: 244–58
   PubMed Web of Science ®Google Scholar
• Cincotta A H, Wilson J M, DeSouza C J. Properly timed injections of cortisol and prolactin produce long-term reductions in obesity, hyperinsulinemia and insulin resistance in the Syrian hamster (Mesocricetus auratus). J Endocrinol. 1989; 120: 385–91
   PubMed Web of Science ®Google Scholar
• Crabtree G R, Munck A, Smith K A. Glucocorticoids and lymphocytes. II. Cell cycle-dependent changes in glucocorticoid receptor content. J Immunol. 1980; 125: 13–17
   PubMedGoogle Scholar
• Cupps T R, Fauci A S. Corticosteroid-mediated immunoregulation in man. Immunol Rev. 1982; 65: 133–55
   PubMed Web of Science ®Google Scholar
• Drozdowicz C K, Bowman T A, Webb M L. Effect of in-house transport on murine plasma corticosterone concentration and blood lymphocyte populations. Am J Vet Res. 1990; 51: 1841–46
   PubMedGoogle Scholar
• Fernandes G. Chronobiology of immune functions: cellular and humoral aspects. Biologic rhythms in clinical and laboratory medicine, Y Touitou, E Haus. Springer-Verlag, Berlin 1992; 493–503
   Google Scholar
• Fernandes G, Carandente F, Halberg E. Circadian rhythm in activity of lympholytic natural killer cells from spleens of Fischer rats. J Immunol. 1979; 123: 622–25
   PubMed Web of Science ®Google Scholar
• Fernandes G, Halberg F, Halberg E. Murine circadian rhythm in natural cell-mediated cytotoxicity against lymphoma cells and chronoimmunology. Chronopharmacology and chronotherapeutics, C A Walker, K FA Soliman, C M Winget. A&M University Foundation, Tallahassee, Florida 1981; 233–45
   Google Scholar
• Fernandes G, Halberg F, Yunis E. Circadian rhythmic plaque-forming cell response of spleens from mice immunized with SRBC. J Immunol. 1976; 117: 962–66
   PubMed Web of Science ®Google Scholar
• Gala R R. Prolactin and growth hormone in the regulation of the immune system. Proc SOC Exp Biol Med. 1991; 198: 513–27
   PubMed Web of Science ®Google Scholar
• Garvy B A, King L E, Telford W G. Chronic elevation of plasma corticosterone causes reductions in the number of cycling cells of the B lineage in murine bone marrow and induces apoptosis. Immunology. 1993; 80: 587–92
   PubMed Web of Science ®Google Scholar
• Giordano M, Vermeulen M, Palermo M S. Seasonal variations in antibody-dependent cellular cytotoxicity regulation by melatonin. FASEB J. 1993; 7: 1052–54
   PubMed Web of Science ®Google Scholar
• Giraldi T, Perissin L, Zorzet S. Metastasis and neuroendocrine system in stressed mice. Int J Neurosci. 1994a; 74: 265–78
   PubMed Web of Science ®Google Scholar
• Giraldi T, Perissin L, Zorzet S. Stress melatonin and tumor progression in mice. Ann NY Acad Sci. 1994b; 719: 526–36
   PubMedGoogle Scholar
• Haus E, Lakatua D J, Swoyer J. Chronobiology in hematology and immunology. Am J Anat. 1983; 168: 467–517
   PubMedGoogle Scholar
• Hayashi O, Kikuchi M. The influence of phase shift in the light-dark cycle on humoral immune responses of mice to sheep red blood cells and polyvinylpyrroli-done. J Immunol. 1985; 134: 1455–61
   PubMedGoogle Scholar
• Hiestand P C, Mekler P, Nordmann R. Prolactin as a modulator of lymphocyte responsiveness provides a possible mechanism of action for cyclosporine. Proc Natl Acad Sci USA. 1986; 83: 2599–2603
   PubMed Web of Science ®Google Scholar
• John T M, Meier A H, Bryant E E. Thyroid hormones and the circadian rhythms of fat and cropsac responses to prolactin in the pigeon. Physiol Zool. 1972; 45: 34–42
   Google Scholar
• Knyszynski A, Fischer H. Circadian rhythm of phagocytic cells in blood, spleen, and peritoneal cavity of mice as measured by zymosan-induced chemilumines-cence. Luminescent assays: perspectives in endocrinology and clinical chemistry, M Serio, M Pazzagli. Raven, New York 1982; 243–49
   Google Scholar
• Kumar Pati A, Florentin I, Chung V. Circannual rhythm in natural killer activity and mitogen responsiveness of murine splenocytes. Cell Immunol. 1987; 108: 227–34
   PubMedGoogle Scholar
• Logan J L, Benson B. Light deprivation retards the growth of the diethylstilbesterol-induced renal tumor in hamsters. Growth Dev Aging. 1990; 54: 39–43
   PubMedGoogle Scholar
• Meier A H. Temporal synergism of prolactin and adrenal steroids. Gen Comp Endocrinol. 1972; 3: 499–508, (Suppl.)
   Google Scholar
• Meier A H. Temporal synergism of circadian neuroendocrine oscillations regulates seasonal conditions in the gulf killifish. Trans Am Fish Soc. 1984; 113: 422–31
   Web of Science ®Google Scholar
• Meier A H. Circadian basis for neuroendocrine regulation. Proceedings International Symposium on Rhythms in Fishes, M A Ali. Plenum, New York 1993; 109–26
   Google Scholar
• Meier A H, Cincotta A H. Circadian rhythms regulate the expression of the thrifty genotype/phenotype. Diab Rev. 1996; 4: 464–87
   Google Scholar
• Meier A H, Ferrell B R, Miller L J. Circadian components of the circannual mechanism in the white-throated sparrow. Acta XVII Congress Internationalis Ornithologia, R Nohring. Verlag Der Deutschen Ornithologen-Gesellschaft, Berlin 1981; 453–62
   Google Scholar
• Meier A H, Fivizzani A J, Spieler R E. Circadian hormone basis for seasonal conditions in the gulf killifish, Fundulus grandis. Comparative endocrinology, P J Gaillard, H H Boer. Elsevier/North Holland Biomedical Press, Amsterdam 1978a; 141–44
   Google Scholar
• Meier A H, Horseman N D. Circadian mechanisms in reproduction. Animal models for research on contraception and fertility, N Alexander. Harper and Row, New York 1978; 33–45
   Google Scholar
• Meier A H, Martin D D, MacGregor R. Temporal synergism of corticosterone and prolactin controlling gonadal growth in sparrows. Science 1971; 173: 1240–42
   PubMed Web of Science ®Google Scholar
• Meier A H, Russo A C. Circadian organization of the avian annual cycle. Current ornithology, R E Johnston. Plenum, New York 1984; 303–43
   Google Scholar
• Meier A H, Trobec T N, Joseph M M. Temporal synergism of prolactin and adrenal steroids in the regulation of fat stores. Proc Soc Exp Biol Med. 1971; 137: 408–15
   Web of Science ®Google Scholar
• Meier A H, Wilson J M. Resetting annual cycles with neurotransmitter-affecting drugs. Environment and hormones, S Ishii, B M Follett, A Schandola. Japan Scientific Society Press; Springer-Verlag, Berlin: Tokyo 1984; 149
   Google Scholar
• Melchart D, Martin P, Hallek M. Circadian variation of the phagocytic activity of polymorphonuclear leukocytes and of various other parameters in 13 healthy male adults. Chronobiol Int. 1992; 9: 3545
   Google Scholar
• Moore-Ede M C. The circadian timing system in mammals: two pacemakers preside over many secondary oscillators. Fed Proc. 1983; 42: 2802–8
   PubMedGoogle Scholar
• Moore-Ede M C, Sulzman F M, Fuller C A. The clocks that time us. Harvard University Press, Cambridge, Massachusetts 1982
   Google Scholar
• Morton M C, Levi F. Circadian-system alterations during cancer processes: a review. Int J Cancer. 1997; 70: 241–47
   PubMedGoogle Scholar
• Council National Research. Guide for care and use of laboratory animals. National Academy Press, Washington, D.C. 1996
   Google Scholar
• Nelson R J, Demas G E, Klein S L. The influence of season, photoperiod, and pineal melatonin on immune function. J Pineal Res. 1995; 19: 149–65
   PubMed Web of Science ®Google Scholar
• Nevid N J, Meier A H. Nonphotic stimuli alter a day-night rhythm of allograft rejection in gulf killifish. Dev Comp Immunol. 1995a; 18: 495–509
   Google Scholar
• Nevid N J, Meier A H. Timed daily administrations of hormones and antagonists of neuroendocrine receptors alter day-night rhythms of allograft rejection in the gulf killifish, Fundulus grundis. Gen Comp Endocrinol. 1995b; 97: 327–39
   PubMedGoogle Scholar
• Nossal G JV. Tolerance and ways to break it. Ann NY Acad Sci. 1993; 690: 34–41
   PubMedGoogle Scholar
• Ormerod M G. Flow Cytometry a practical approach. Oxford University Press, New York 1994
   Google Scholar
• Reinberg A E. Concepts in chronopharmacology. Annu Rev Pharmacol Toxicol. 1992; 32: 51–66
   PubMed Web of Science ®Google Scholar
• Rockwell S C, Kallman R F. Cellular radiosensitivity and tumor radiation response in the EMT6 tumor cell system. Radiat Res. 1973; 53: 281–94
   PubMed Web of Science ®Google Scholar
• Rockwell S C, Kallman R F, Fajordo L F. Characteristics of a serially transplanted mouse mammary tumor and its tissue culture adapted derivative. J Natl Cancer Inst. 1972; 49: 1735–49
   Google Scholar
• Rosenwasser A M, Adler N T. Structure and function in circadian timing systems: evidence for multiple coupled circadian oscillators. Neurosci Biobehav Rev. 1986; 10: 431–48
   PubMed Web of Science ®Google Scholar
• Screpanti I, Morrone S, Meco D. Steroid sensitivity of thymocyte subpopulations during intrathymic differentiation. Effects of 17 beta-estradiol and dexamethasone on subsets expressing T cell antigen receptor or IL-2 receptor. J Immunol. 1989; 142: 3378–83
   PubMed Web of Science ®Google Scholar
• Stanberry L R, Das Gupta T K, Beattie C W. Photoperiodic control of melanoma growth in hamsters: influence of pinealectomy and melatonin. Endocrinology. 1983; 113: 469–75
   PubMed Web of Science ®Google Scholar
• Von Roemeling R, DeMaria L, Salzer M. Circadian stage dependent response to IL-2 in mouse spleen and bone marrow. Annual review of chronopharmacology, A Reinberg, M Smolensky, G Labreque. Pergamon, OxfordU.K. 1990; Vol. 7: 211
   Google Scholar
• Waldman T, Zhang Y, Dillehay L. Cell-cycle arrest versus cell death in cancer therapy. Nature Med. 1997; 3: 1034–36
   PubMed Web of Science ®Google Scholar
• Waldrop R D, Saydjari R, Rubin N H. Photoperiod influences the growth of colon cancer in mice. Life Sci. 1989; 45: 737–44
   PubMedGoogle Scholar
• Williams R M, Kraus L J, Inbar M. Circadian bioperiodicity of natural killer cell activity in human blood (individually assessed). Chronopharmacology and chronotherapeutics, C A Walker, C M Winget, K FA Soliman. A&M University Foundation, Tallahassee, Florida 1981; 269–73
   Google Scholar
• Zapata A G, Varas A, Torroba M. Seasonal variations in the immune system of lower vertebrates. Immunol Today. 1992; 13: 142–47
   PubMedGoogle Scholar