Steroid-induced androgen receptor-oestradiol receptor ß-Src complex triggers prostate cancer cell proliferation.

Treatment of human prostate carcinoma-derived LNCaP cells with androgen or oestrediol triggers simultaneous association of androgen receptor and oestradiol receptor β with Src, activates the Src/Raf-1/ Erk-2 pathway and stimulates cell proliferation. Surprisingly, either androgen or oestradiol action on each of these steps is inhibited by both anti-androgens and anti-oestrogens. Similar findings for oestradiol receptor a were observed in MCF-7 or T47D cells stimulated by either oestrediol or androgens. Micro-injection of LNCaP, MCF-7 and T47D cells with SrcK-abolishes steroid-stimulated S-phase entry. Data from transfected Cos cells confirm and extend the findings from these cells. Hormone-stimulated Src interaction with the androgen receptor and oestradiol receptor α or β is detected using glutathione S-transferose fusion constructs. Src SH2 interacts with phosphotyrosine 537 of oestradiol receptor α and the Src SH3 domain with a proline-rich stretch of the androgen receptor. The role of this phosphotyrosine is stressed by its requirement for association of oestradiol receptor α with Src and consequent activation of Src in intact Cos cells. [ABSTRACT FROM AUTHOR]