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口服脱氢表雄酮可抑制裸鼠体内人胰腺癌的生长。

Oral dehydroepiandrosterone inhibits the growth of human pancreatic cancer in nude mice.

作者信息

Muscarella P, Boros L G, Fisher W E, Rink C, Melvin W S

机构信息

Department of Surgery, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

J Surg Res. 1998 Oct;79(2):154-7. doi: 10.1006/jsre.1998.5417.

Abstract

BACKGROUND

Dehydroepiandrosterone (DHEA), an androgen precursor, inhibits the induction of pancreatic cancer in some animal models. Our laboratory has previously demonstrated that the sulfated form of DHEA (DHAS), when administered by intraperitoneal injection, inhibits the growth of pancreatic cancer xenografts in nude mice. In the present study, we hypothesize that DHEA-mediated pancreatic cancer growth inhibition is associated with alterations in plasma sex hormone concentrations.

MATERIALS AND METHODS

Forty male, nude, athymic mice were fed either Teklad 22/5 rodent diet or diet supplemented with 0.6% DHEA ad libitum. Four weeks following the institution of the experimental diets, 1 x 10(6) MiaPaCa-2 cells were injected into the right flank of each animal. Tumor area was recorded weekly and tumor weights were measured after 5 weeks. Plasma DHAS, testosterone, and progesterone concentrations were determined by radioimmunoassay.

RESULTS

Plasma DHAS, testosterone, and progesterone concentrations were all significantly elevated in the DHEA-treated group. DHEA-treated mouse plasma DHAS concentrations were approximately 50-fold higher than controls. Mean tumor weight was significantly reduced in the DHEA group (68.9 +/- 39.1 vs 121.0 +/- 64.3). DHEA treatment did not result in significant animal weight reductions and toxic side effects were not observed.

CONCLUSIONS

Dietary supplementation with 0.6% DHEA causes significant elevations in plasma DHAS concentration. DHEA administration significantly inhibits pancreatic cancer cell growth at plasma concentrations 1 x 10(5)-fold lower than previously reported. The mechanism of action may involve elevated concentrations of sex hormones.

摘要

背景

脱氢表雄酮(DHEA),一种雄激素前体,在一些动物模型中可抑制胰腺癌的诱发。我们实验室之前已经证明,硫酸化形式的DHEA(DHAS)腹腔注射时可抑制裸鼠体内胰腺癌异种移植瘤的生长。在本研究中,我们假设DHEA介导的胰腺癌生长抑制与血浆性激素浓度的改变有关。

材料与方法

40只雄性裸鼠随意喂食Teklad 22/5啮齿动物饲料或补充0.6% DHEA的饲料。开始实验性饮食4周后,将1×10⁶个MiaPaCa - 2细胞注射到每只动物的右腹侧。每周记录肿瘤面积,5周后测量肿瘤重量。通过放射免疫分析法测定血浆中DHAS、睾酮和孕酮的浓度。

结果

DHEA处理组的血浆DHAS、睾酮和孕酮浓度均显著升高。DHEA处理的小鼠血浆DHAS浓度比对照组高约50倍。DHEA组的平均肿瘤重量显著降低(68.9±39.1对121.0±64.3)。DHEA处理未导致动物体重显著减轻,也未观察到毒副作用。

结论

饮食中补充0.6% DHEA可使血浆DHAS浓度显著升高。给予DHEA在血浆浓度比先前报道低1×10⁵倍时即可显著抑制胰腺癌细胞生长。作用机制可能涉及性激素浓度升高。

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