• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

AXC/SSh大鼠前列腺癌细胞在体外的增殖受雄激素调节。

Proliferation of AXC/SSh rat prostate cancer cells in vitro is androgen modulated.

作者信息

Shain S A, Huot R I

机构信息

Department of Cellular and Molecular Biology, Southwest Foundation for Biomedical Research, San Antonio, TX 78284.

出版信息

J Steroid Biochem. 1987;27(1-3):503-12. doi: 10.1016/0022-4731(87)90347-5.

DOI:10.1016/0022-4731(87)90347-5
PMID:3320541
Abstract

We used heterogeneous parental cultures of AXC/SSh rat prostate cancer cells to isolate clonally derived prostate cancer cell lines. Light and electron microscopic analyses established that parental and clonally isolated cells possess features characteristic of secretory epithelium. Biochemical analyses showed that these cells contained androgen receptors and acid phosphatase and 5 alpha-reductase activity; phenotypic markers characteristic of differentiated prostate epithelium. Content of these prostate epithelial cell markers was variable and cell line specific. We used selected cell lines to examine androgen modulation of AXC/SSh rat prostate cancer cell proliferation in vitro. We found that proliferation of C-family or D-family cells, those respectively maintained on medium without additions or medium containing 10(-7) M 5 alpha-dihydrotestosterone, was not affected by changes in medium testosterone concentration through the range 10(-6)-10(-9) M. In contrast, testosterone modified proliferation of T-family cells, those maintained on medium containing 10(-7) M testosterone, and effects were antagonized by the anti-androgen RU 23908. Preliminary studies established that AXC/SSh rat prostate cancer cells elaborate polypeptide components which stimulate in vitro cell proliferation. Both the ability to elaborate these components and their effects on in vitro cell proliferation appeared to be cell line specific.

摘要

我们使用AXC/SSh大鼠前列腺癌细胞的异质亲本培养物来分离克隆衍生的前列腺癌细胞系。光学和电子显微镜分析表明,亲本细胞和克隆分离的细胞具有分泌上皮的特征。生化分析表明,这些细胞含有雄激素受体、酸性磷酸酶和5α-还原酶活性;这些是分化前列腺上皮的表型标志物。这些前列腺上皮细胞标志物的含量是可变的,且具有细胞系特异性。我们使用选定的细胞系来研究雄激素对AXC/SSh大鼠前列腺癌细胞体外增殖的调节作用。我们发现,C家族或D家族细胞(分别在无添加物的培养基或含有10^(-7) M 5α-双氢睾酮的培养基中培养)的增殖不受培养基中睾酮浓度在10^(-6)-10^(-9) M范围内变化的影响。相比之下,睾酮改变了T家族细胞(在含有10^(-7) M睾酮的培养基中培养)的增殖,且这些作用可被抗雄激素RU 23908拮抗。初步研究表明,AXC/SSh大鼠前列腺癌细胞能分泌刺激体外细胞增殖的多肽成分。分泌这些成分的能力及其对体外细胞增殖的影响似乎都具有细胞系特异性。

相似文献

1
Proliferation of AXC/SSh rat prostate cancer cells in vitro is androgen modulated.AXC/SSh大鼠前列腺癌细胞在体外的增殖受雄激素调节。
J Steroid Biochem. 1987;27(1-3):503-12. doi: 10.1016/0022-4731(87)90347-5.
2
Differential androgen modulation of AXC/SSh rat prostate cancer cell proliferation in vitro and its antagonism by antiandrogen.雄激素对AXC/SSh大鼠前列腺癌细胞体外增殖的差异调节及其抗雄激素的拮抗作用。
Cancer Res. 1986 Aug;46(8):3775-81.
3
Biochemical and morphological characterization of clonal AXC rat prostate cancer cells.克隆性AXC大鼠前列腺癌细胞的生化与形态学特征
Cancer Res. 1984 May;44(5):2033-42.
4
Differential metabolism of dehydroepiandrosterone sulfate and estrogen conjugates by normal or malignant AXC/SSh rat prostate cells and effects of these steroid conjugates on cancer cell proliferation in vitro.
J Steroid Biochem. 1988 Jun;29(6):617-21. doi: 10.1016/0022-4731(88)90160-4.
5
Differences in responsiveness of clonally derived AXC/SSh rat prostate cancer cells to secreted or prototypic mitogens.克隆衍生的AXC/SSh大鼠前列腺癌细胞对分泌型或原型有丝分裂原反应性的差异。
Cancer Res. 1989 Jul 15;49(14):3898-903.
6
Neither fibroblast growth factor-1 nor fibroblast growth factor-2 is an androgen receptor coactivator in androgen-resistant prostate cancer.在雄激素抵抗性前列腺癌中,成纤维细胞生长因子-1和成纤维细胞生长因子-2均不是雄激素受体共激活因子。
Mol Urol. 2001 Autumn;5(3):121-30. doi: 10.1089/10915360152559602.
7
Antiandrogen effects in models of androgen responsive cancer.
J Steroid Biochem. 1988 Oct;31(4B):711-8. doi: 10.1016/0022-4731(88)90022-2.
8
Androgen modulation of prostate cancer cell androgen receptor content is cell line specific.雄激素对前列腺癌细胞雄激素受体含量的调节具有细胞系特异性。
Mol Cell Endocrinol. 1989 May;63(1-2):75-83. doi: 10.1016/0303-7207(89)90083-x.
9
Heparin-binding keratinocyte growth factor is a candidate stromal-to-epithelial-cell andromedin.肝素结合角质形成细胞生长因子是一种潜在的基质细胞与上皮细胞之间的雄激素介质。
Mol Endocrinol. 1992 Dec;6(12):2123-8. doi: 10.1210/mend.6.12.1491693.
10
Antiandrogenic effects of novel androgen synthesis inhibitors on hormone-dependent prostate cancer.新型雄激素合成抑制剂对激素依赖性前列腺癌的抗雄激素作用
Cancer Res. 2000 Dec 1;60(23):6630-40.