Minasian-Batmanian L C, Jabara A G
Br J Cancer. 1981 Jun;43(6):832-41. doi: 10.1038/bjc.1981.122.
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.
在患有持续生长的二甲基苯并蒽(DMBA)诱导的乳腺肿瘤且对双侧肾上腺卵巢切除术(Ax + Ox)有反应的大鼠中,研究了激素和药物治疗对血浆催乳素(PRL)水平和乳腺肿瘤生长的影响。给予雌激素(E2)可使血浆PRL和肿瘤生长均增加,但当同时注射麦角隐亭(Eg)使PRL水平降低时,E2无法维持肿瘤生长。奋乃静(Pz)可使血浆PRL呈剂量相关增加,但在没有E2的情况下刺激肿瘤生长需要Pz诱导的最低血浆PRL水平(0.15 mg/100 g体重/天或更高)。单独使用孕酮(P)(3 mg/天),尽管对PRL水平无影响,但无论治疗持续时间如何,均可维持肿瘤静态生长(即有轻微刺激作用)。在Ax + Ox对照组中,注射联合使用的P + Pz(0.1 mg/100 g/天)后,血浆PRL水平高于基础值的升高足以维持肿瘤静态生长,但不足以重新激活生长。直到联合注射P和更高剂量的Pz(0.3 mg/100 g/天)时,血浆PRL和肿瘤生长才会增强;然而,这种治疗虽然无法刺激肿瘤持续生长,但当同时注射P + Pz + Eg使血浆PRL降低时,能够维持静态生长。根据这些发现推测,P维持肿瘤静态生长的作用机制与PRL不同,且独立于循环PRL水平。