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雌激素受体-β下调与人类睾丸精原细胞瘤中转录共调节因子 PATZ1 易位相关。

Down-regulation of oestrogen receptor-β associates with transcriptional co-regulator PATZ1 delocalization in human testicular seminomas.

机构信息

Dipartimento di Medicina Sperimentale, II Università di Napoli, Naples, Italy.

出版信息

J Pathol. 2011 May;224(1):110-20. doi: 10.1002/path.2846. Epub 2011 Mar 7.

DOI:10.1002/path.2846
PMID:21381029
Abstract

Oestrogen exposure has been linked to a risk for the development of testicular germ cell cancers. The effects of oestrogen are now known to be mediated by oestrogen receptor-α (ERα) and ERβ subtypes, but only ERβ has been found in human germ cells of normal testis. However, its expression was markedly diminished in seminomas, embryonal cell carcinomas and mixed germ cell tumours, but remains high in teratomas. PATZ1 is a recently discovered zinc finger protein that, due to the presence of the POZ domain, acts as a transcriptional repressor affecting the basal activity of different promoters. We have previously described that PATZ1 plays a crucial role in normal male gametogenesis and that its up-regulation and mislocalization could be associated with the development of testicular germ cell tumours. Here we show that ERβ interacts with PATZ1 in normal germ cells, while down-regulation of ERβ associates with transcriptional co-regulator PATZ1 delocalization in human testicular seminomas. In addition, we show that the translocation of PATZ1 from the cytoplasm into the nucleus is regulated by cAMP, which also induces increased expression and nuclear localization of ERβ, while this effect is counteracted by using the anti-oestrogen ICI 182-780.

摘要

雌激素暴露与睾丸生殖细胞癌的发生风险有关。现在已知雌激素的作用是通过雌激素受体-α(ERα)和 ERβ 亚型介导的,但仅在正常睾丸的人类生殖细胞中发现了 ERβ。然而,在精原细胞瘤、胚胎性细胞癌和混合性生殖细胞肿瘤中,其表达明显减少,但在畸胎瘤中仍保持高水平。PATZ1 是一种新发现的锌指蛋白,由于存在 POZ 结构域,它作为转录抑制剂发挥作用,影响不同启动子的基础活性。我们之前曾描述过,PATZ1 在正常男性配子发生中起着至关重要的作用,其上调和定位错误可能与睾丸生殖细胞肿瘤的发生有关。在这里,我们表明 ERβ 在正常生殖细胞中与 PATZ1 相互作用,而 ERβ 的下调与人类睾丸精原细胞瘤中转录共调节剂 PATZ1 的定位错误有关。此外,我们还表明,PATZ1 从细胞质向细胞核的易位受 cAMP 调节,cAMP 还诱导 ERβ 的表达增加和核定位,而这种效应被使用抗雌激素 ICI 182-780 所抵消。

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