Abstract

The effects of hormone and drug treatments on plasma prolactin (PRL) levels and mammary tumour growth were investigated in rats bearing continuously growing DMBA-induced mammary tumours that responded to bilateral adreno-ovariectomy (Ax + Ox), Oestrogen (E2) administration increased both plasma PRL and tumour growth, but was unable to sustain tumour growth when the PRL level was reduced by concurrent injection of ergocornine (Eg). Perphenazine (Pz) produced a dose-related increase in plasma PRL, but stimulation of tumour growth in the absence of E2 required a minimal level of plasma PRL induced by Pz (0.15 mg/100 g body wt/day or more). Progesterone (P) (3 mg/day) alone, although without effect on PRL levels, maintained static tumour growth (i.e. it had a slight stimulatory effect) irrespective of the duration of treatment. The increase in plasma PRL levels above the basal values in the Ax + Ox controls following injections of combined P + Pz (0.1 mg/100 g/day) was sufficient to sustain static tumour growth, but not to reactivate growth. Enhancement of both plasma PRL and tumour growth did not occur until P and higher doses of Pz (0.3 mg/100 g/day) were injected jointly; this treatment, however, while unable to stimulate continuous tumour growth, was able to maintain static growth when plasma PRL was reduced by concurrent injections of P + Pz + Eg. From these findings it is postulated that the mechanism of action whereby P maintains static tumour growth is different from that of PRL and independent of circulating PRL levels.

Highlights

  • Summary.-The effects of hormone and drug treatments on plasma prolactin (PRL) levels and mammary tumour growth were investigated in rats bearing continuously growing dimethylbenz - (a) - anthracene (DMBA)-induced mammary tumours that responded to bilateral adrenoovariectomy (Ax+ Ox)

  • (330%) rats bearing neoplasms showed a continuous growth pattern for at least one of their tumours, and only 40 (79%o) of these responded to Ax +Ox by a marked regression in their size, indicating their hormone-dependence

  • These hormone-responsive neoplasms were used in the present experiments

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Summary

Introduction

Summary.-The effects of hormone and drug treatments on plasma prolactin (PRL) levels and mammary tumour growth were investigated in rats bearing continuously growing DMBA-induced mammary tumours that responded to bilateral adrenoovariectomy (Ax+ Ox). Oestrogen (E2) administration increased both plasma PRL and tumour growth, but was unable to sustain tumour growth when the PRL level was reduced by concurrent injection of ergocornine (Eg). The dose-effect relationship of PRL on mammary tumour growth and the duration of PRL-induced stimulation of tumour growth, in the Ax + Ox rat, is a matter of debate. Reported plasma PRL levels in rats bearing DMBA-induced mammary cancers is contradictory, both normal (Nagasawa et al, 1973) and raised values having been found (Teller et al, 1977). Of P receptor (i.e., their results suggested that E2 is an absolute necessity at the tumour site). Kelly et al (1977), on the other hand, reported a similar effect of

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