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一种新的前列腺增生小鼠模型:通过胎儿泌尿生殖窦植入诱导成年前列腺过度生长。

A new mouse model for prostatic hyperplasia: induction of adult prostatic overgrowth by fetal urogenital sinus implants.

作者信息

Chung L W, Matsuura J, Rocco A K, Thompson T C, Miller G J, Runner M N

出版信息

Prog Clin Biol Res. 1984;145:291-306.

PMID:6201880
Abstract

A new mouse model for human BPH has been established. This model was developed on the basis that fetal and adult prostatic cells interact to induce the proliferation of adult prostatic cells. A 10- to 20-fold overgrowth of the adult mouse prostate gland can be induced by implantation of fetal UGS into the adult prostate gland. Components of UGS, fetal UGM, and fetal UGE may be involved in the regulation of adult prostatic overgrowth. The androgen dependency and the specificity (donor tissue, site of implantation, and strain and species) of UGS-induced adult prostatic overgrowth have also been established. The question remains whether the prostatic hyperplasia seen in this mouse model may be representative of human BPH. The observation that fetal UGS implants induce adult prostatic overgrowth in the complete absence of exogenous sex steroids support the hypothesis of McNeal that human BPH may develop as a result of the reactivation of fetal growth potential in the periurethral area of the adult prostate gland. The present mouse model may be used as a test system for the future development of anti-BPH drugs.

摘要

一种新的人类良性前列腺增生小鼠模型已经建立。该模型是基于胎儿和成年前列腺细胞相互作用以诱导成年前列腺细胞增殖而开发的。将胎儿尿道生殖窦(UGS)植入成年前列腺可诱导成年小鼠前列腺出现10至20倍的过度生长。UGS的组成部分,即胎儿尿道生殖窦基质(UGM)和胎儿尿道生殖窦上皮(UGE),可能参与成年前列腺过度生长的调节。UGS诱导的成年前列腺过度生长的雄激素依赖性以及特异性(供体组织、植入部位以及品系和物种)也已得到证实。该小鼠模型中出现的前列腺增生是否可代表人类良性前列腺增生这一问题仍然存在。胎儿UGS植入在完全没有外源性性类固醇的情况下诱导成年前列腺过度生长这一观察结果支持了麦克尼尔的假说,即人类良性前列腺增生可能是由于成年前列腺尿道周围区域胎儿生长潜能的重新激活所致。目前的小鼠模型可作为未来抗良性前列腺增生药物开发的测试系统。

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