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.
| Original language | English |
|---|---|
| Pages (from-to) | 110-20 |
| Number of pages | 11 |
| Journal | The Journal of pathology |
| Volume | 224 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - May 2011 |
| Externally published | Yes |
Keywords
- Antineoplastic Agents, Hormonal/pharmacology
- Cell Nucleus/metabolism
- Cyclic AMP/pharmacology
- Cytoplasm/metabolism
- Down-Regulation
- Estradiol/analogs & derivatives
- Estrogen Antagonists/pharmacology
- Estrogen Receptor beta/metabolism
- Fulvestrant
- Gene Expression Regulation, Neoplastic
- Humans
- Kruppel-Like Transcription Factors/genetics
- Male
- Neoplasm Proteins/metabolism
- Repressor Proteins/genetics
- Seminoma/metabolism
- Testicular Neoplasms/metabolism
- Translocation, Genetic/drug effects
- Tumor Cells, Cultured