EFFECT OF ESTRADIOL AND PROGESTERONE ON THE ADENYLATE CYCLASE ACTIVITY IN GRAFTS OF 3‐METHYLCHOLANTHRENE INDUCED CARCINOMAS IN THE MOUSE UTERINE CERVIX

Grafts from a methylcholanthrene induced mouse uterine cervical carcinoma (NMRI mice) were grown in neonatal female mouse hosts. The hosts were treated for 12 days with estradiol and progesterone alone or in combination. Controls were injected with the solvent (olive oil) only. Pieces from every graft were used for histological study, for study of the proliferation rate and for study of the adenylate cyclase activity in homogenate. All the grafts were well differentiated squamous carcinomas and the histological picture was the same irrespective of hormonal treatment. The proliferation rate was the same in control grafts as in those from hosts treated with hormones. Grafts from progesterone and progesterone/estradiol injected hosts had significantly higher levels of adenylate cyclase activity compared with grafts from control hosts. Estradiol alone resulted in a trend towards increased activity but the difference to controls was not statistically significant.

[1]  S. Kvinnsland Adenylate cyclase activity in the uterine cervix of neonatal and immature mice: influence of oestradiol-17 beta. , 1980, The Journal of endocrinology.

[2]  E. Baulieu Cell membrane, a target for steroid hormones , 1978, Molecular and Cellular Endocrinology.

[3]  T. Christoffersen,et al.  Effect of prostaglandins and hormones on cyclic AMP formation in rat hepatomas and liver tissue. , 1978, British Journal of Cancer.

[4]  J. Gray,et al.  Regulation of S49 lymphoma cell growth by cyclic adenosine 3':5'-monophosphate. , 1978, Cancer research.

[5]  R. Niles,et al.  Hormonal activation of adenylate cyclase in mouse melanoma metastatic variants , 1978, Journal of cellular physiology.

[6]  P. Ueland,et al.  The Isozyme Pattern of Cyclic Amp‐Dependent Protein Kinase and the Distribution of a Cervicovaginal Antigen in Experimental Carcinoma of the Cervix Uteri of Mice , 1978, Acta pathologica et microbiologica Scandinavica. Section A, Pathology.

[7]  C. Chew,et al.  Uterine cyclic AMP formation: biphasic effect of estrogen on catecholamine sensitivity. , 1978, Life sciences.

[8]  Y. Cho‐Chung,et al.  Cyclic AMP-binding proteins: inverse relationship with estrogen-receptors in hormone-dependent mammary tumor regression. , 1978, European journal of biochemistry.

[9]  J. A. Rillema,et al.  Cyclic nucleotides and their associated enzymes in 9,10-dimethyl-1,2-benzanthracene-induced mammary tumors of rats. , 1978, Cancer research.

[10]  J. W. Osborne,et al.  Cyclic nucleotide concentrations in 1,2-dimethylhydrazine induced rat colon adenocarcinoma. , 1978, Cancer letters.

[11]  T. Martin,et al.  Adenylate cyclase activity of renal cortical carcinoma and its relation to histology and ultrastructure. , 1978, Cancer research.

[12]  Y. Cho‐Chung,et al.  Adenylate cyclase, cyclic adenosin 3':5'-monophosphate phosphodiesterase, and regression of Walker 256 mammary carcinoma. , 1977, Cancer research.

[13]  J. Torhorst,et al.  Altered levels of cyclic nucleotides, cyclic AMP phosphodiesterase and adenylyl cyclase activities in normal, dysplastic and neoplastic human mammary tissue , 1977, FEBS letters.

[14]  Y. Cho‐Chung,et al.  Altered cyclic AMP-binding and db cyclic AMP-unresponsiveness in vivo , 1977, Nature.

[15]  P. Muganda,et al.  Cyclic nucleotide metabolism in solid tumor tissues. , 1977, Advances in experimental medicine and biology.

[16]  R. A. Hickie Regulation of cyclic AMP and cyclic GMP in Morris hepatomas and liver. , 1977, Advances in experimental medicine and biology.

[17]  J. Forsberg,et al.  A synergistic effect of oestradiol and prolactin influencing the incidence of 3-methylcholanthrene induced cerivical carcinomas in mice. , 2009, Acta pathologica et microbiologica Scandinavica. Section A, Pathology.

[18]  F. Martin,et al.  HYPOTHALAMIC HYPOPITUITARISM FOLLOWING EXTERNAL RADIOTHERAPY FOR TUMOURS DISTANT FROM THE ADENOHYPOPHYSIS , 1976, Clinical endocrinology.

[19]  F. DeRubertis,et al.  The content and metabolism of cyclic adenosine 3', 5'-monophosphate and cyclic guanosine 3', 5'-monophosphate in adenocarcinoma of the human colon. , 1976, The Journal of clinical investigation.

[20]  R. Matusik,et al.  Relationship of adenosine 3',5'-cyclic monophosphate and guanosine 3',5'-cyclic monophosphate to growth of dimethylbenz(a)anthracene-induced mammary tumors in rats. , 1976, Journal of the National Cancer Institute.

[21]  T. Martin,et al.  HORMONE RECEPTORS AND CYCLIC NUCLEOTIDE METABOLISM IN CANCER CELLS , 1976, Clinical endocrinology.

[22]  B. Alberts,et al.  Steroid receptors: elements for modulation of eukaryotic transcription. , 1976, Annual review of biochemistry.

[23]  R. Pietras,et al.  Surface modifications evoked by estradiol and diethylstilbestrol in isolated endometrial cells: evidence from lectin probes and extracellular release of lysosomal protease. , 1975, Endocrinology.

[24]  J. Gray,et al.  Cyclic AMP, a nonessential regulator of the cell cycle. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[25]  P. Chan,et al.  Intracellular cAMP levels in normal rat mammary gland and adenocarcinoma. In vivo vs in vitro. , 1975, Life sciences.

[26]  C. Londos,et al.  A highly sensitive adenylate cyclase assay. , 1974, Analytical biochemistry.

[27]  S. Reboud,et al.  Co-carcinogenic Effect of Progesterone on 20-Methylcholan-threne Induced Cervical Carcinoma in Mice , 1973, Nature.

[28]  J. Forsberg,et al.  Carcinogenesis with 3-methylcholanthrene in uterine cervix of mice treated neonatally with estrogen. , 1972, Journal of the National Cancer Institute.

[29]  J. Sheppard Difference in the cyclic adenosine 3',5'-monophosphate levels in normal and transformed cells. , 1972, Nature: New biology.

[30]  J. Raymond [Cyclic AMP]. , 1972, La Nouvelle presse medicale.

[31]  W. Ryan,et al.  Cyclic nucleotides on cell growth in vitro. , 1970, Cancer research.

[32]  H. Spjut,et al.  Adenylcyclase activity in dimethylamino biphenyl-induced breast carcinoma. , 1969, Biochimica et biophysica acta.

[33]  L. Klungsöyr Quantitative estimation of protein. Separation of alkaline protein-copper complex from excess copper on Sephadex G-25. , 1969, Analytical biochemistry.

[34]  A. Mannan,et al.  Effect of ovariectomy on the fate of 20-methyl-cholanthrene induced dysplasia of the mouse uterine cervix. , 1968, Acta cytologica.

[35]  H. Zaman,et al.  Effect of ovariectomy on the induction by 20-methylcholanthrene of carcinoma of the mouse uterine cervix. , 1967, Acta cytologica.

[36]  I. Nagata,et al.  Effect of estrogen on the uterine cancer induced by 20-methylcholanthrene (from the autoradiographic observation). , 1966, Gan.

[37]  A. Glucksmann,et al.  The Effect of Castration and of Additional Hormonal Treatments on the Induction of Cervical and Vulval Tumours in Mice , 1962, British Journal of Cancer.

[38]  N. Kaufman,et al.  Neoplastic changes in cervixuteri following administration of estradiol-benzoate and 20-methylcholanthrene. , 1962, Acta cytologica.

[39]  E. Murphy Carcinogenesis of the uterine cervix in mice: effect of diethylstilbestrol after limited application of 3-methylcholanthrene. , 1961, Journal of the National Cancer Institute.

[40]  S. L. Bonting,et al.  Determination of microgram quantities of deoxyribonucleic acid and protein in tissues grown in vitro. , 1957, Archives of biochemistry and biophysics.