DNA-SYNTHESIS BY PITUITARY-TUMORS, WITH REFERENCE TO PLASMA-HORMONE LEVELS AND TO EFFECTS OF BROMOCRIPTINE

被引:9
作者
LLOYD, HM
JACOBI, JM
WILLGOSS, DA
机构
[1] UNIV QUEENSLAND,ROYAL BRISBANE HOSP,DEPT MED,BRISBANE,QLD 4029,AUSTRALIA
[2] UNIV QUEENSLAND,ROYAL BRISBANE HOSP,DEPT CHEM PATHOL,HERSTON,QLD 4029,AUSTRALIA
关键词
D O I
10.1111/j.1365-2265.1995.tb01896.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND AND OBJECTIVE In parathyroid adenomas and experimentally In the normal rat pituitary gland, cell replication and secretory activity were previously shown to be correlated. A similar relationship has now been investigated in human pituitary tumours, since this could have relevance to their growth and aetiology. The effect of bromocriptine on the two variables was examined. PATIENTS Data were derived from 50 patients undergoing operation for pituitary tumour, including 15 with acromegaly and 11 with prolactinoma. MEASUREMENTS Preoperative plasma levels of GH, PRL and gonadotrophins were measured by radioimmunoassay. DNA synthesis, an index of cell replication, was measured in vitro in freshly removed tumour tissue. Nuclear diameter of tumour cells was measured in histological sections and immunostaining for relevant hormones was carried out on tumour tissue. RESULTS DNA synthesis was correlated (P<0.05) with plasma hormone levels in cases of prolactinoma, both treated and not treated with bromocriptine, and in a group of putative FSH secreting tumours from male patients. The correlation was not significant in cases of acromegaly. Comparisons of mean values between groups treated and not treated with bromocriptine showed significantly lower DNA synthesis and mean nuclear diameter in prolactinomas under treatment but not in GH secreting tumours. CONCLUSIONS The findings in prolactinomas suggest a close relationship between secretion and tumour cell replication dependent on still undefined agents, but including dopamine, affecting both variables, and isoforms of PRL, which may stimulate or inhibit replication of PRL secreting cells. The basis of the relationship in FSH secreting tumours is unknown. The relationship was absent in the non-homogeneous group of GH secreting tumours. When secretion and growth are correlated, the secretory process may be the site of the primary abnormality in the tumour cell. Evidence that bromocriptine inhibits tumour cell replication was obtained for prolactinomas but not for on secreting tumours.
引用
收藏
页码:79 / 85
页数:7
相关论文
共 36 条
  • [1] INHIBITORY-ACTION OF BROMOCRIPTINE AND TAMOXIFEN ON THE GROWTH OF HUMAN PITUITARY-TUMORS IN SOFT AGAR
    ARAFAH, BM
    WILHITE, BL
    RAINIERI, J
    BRODKEY, JS
    PEARSON, OH
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1983, 57 (05) : 986 - 992
  • [2] BESSER M, 1993, ACTA ENDOCRINOL-COP, V129, P27
  • [3] BEVAN J S, 1991, British Journal of Neurosurgery, V5, P3, DOI 10.3109/02688699108998439
  • [4] GROWTH HORMONE-RELEASING FACTOR STIMULATES PROLIFERATION OF SOMATOTROPHS INVITRO
    BILLESTRUP, N
    SWANSON, LW
    VALE, W
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (18) : 6854 - 6857
  • [5] PITUITARY-ADENOMA PROLIFERATIVE INDEXES AND RISK OF RECURRENCE
    CARBONI, P
    DETTA, A
    HITCHCOCK, ER
    POSTANS, R
    [J]. BRITISH JOURNAL OF NEUROSURGERY, 1992, 6 (01) : 33 - 40
  • [6] FAILURE OF DOPAMINE AND BROMOCRIPTINE TO AFFECT PROLACTIN-RELEASE AND CELL-GROWTH IN THE DOPAMINE RECEPTOR-DEFICIENT 235-1 CLONE
    CRONIN, MJ
    PERKINS, SN
    KEEFER, DA
    MACLEOD, RM
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1982, 28 (02) : 229 - 246
  • [7] DNA-SYNTHESIS AND SECRETION OF PROLACTIN AND GROWTH-HORMONE BY PITUITARY-GLAND OF MALE RAT - EFFECTS OF DIETHYLSTILBESTROL AND 2-BROMO-ALPHA-ERGOCRYPTINE METHANESULFONATE
    DAVIES, C
    JACOBI, J
    LLOYD, HM
    MEARES, JD
    [J]. JOURNAL OF ENDOCRINOLOGY, 1974, 61 (03) : 411 - 417
  • [8] DREWETT N, 1993, NEUROENDOCRINOLOGY, V57, P89
  • [9] FLORIO T, 1992, J BIOL CHEM, V267, P24169
  • [10] PITUITARY-ADENOMAS - LONG-TERM RESULTS FOR RADIOTHERAPY ALONE AND POSTOPERATIVE RADIOTHERAPY
    HUGHES, MN
    LLAMAS, KJ
    YELLAND, ME
    TRIPCONY, LB
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1993, 27 (05): : 1035 - 1043