Estrogens promote proliferation of the seminoma-like TCam-2 cell line through a GPER-dependent ERα36 induction.

Angelina Wallacides (1) , Amand Chesnel (1) , Hussein Ajj (1) , Martine Chillet (1) , Stéphane Flament (1) , Hélène Dumond (1)

1 SIGRETO - Signalisation, Génomique et Recherche Translationnelle en Oncologie

Seminoma, originated from carcinoma in situ cells (CIS), is one of the main causes of cancer in young men. Postpubertal development of these testicular germ cell tumors suggests a hormone-sensitive way of CIS cell proliferation induction. Using the unique seminoma TCam-2 cell line, we demonstrate that both estradiol and testosterone can stimulate TCam-2 cell proliferation in the absence of the estradiol receptor ERα. We establish that estradiol can activate GPER-cAMP/PKA signalling pathway. TCam-2 cells express ERα36, a truncated isoform of the canonical ERα receptor, the expression of which is rapidly induced after estrogen treatment in a GPER-dependent manner. ERα36 knockdown indicates that ERα36 is (i) a downstream target of E(2)-activated GPER/PKA/CREB pathway, (ii) required for estradiol-dependent EGFR expression, (iii) necessary for cell proliferation. Colocalization of ERα36 with cytoskeleton microfilaments suggests a role of estrogens in cell motility. Our results highlight the functional role of ERα36 in context of seminoma cell proliferation and the importance of testing ERα36 in vivo as a possible future prognostic marker.

Domaines: Endocrinologie et métabolisme

Angelina Wallacides, Amand Chesnel, Hussein Ajj, Martine Chillet, Stéphane Flament, et al.. Estrogens promote proliferation of the seminoma-like TCam-2 cell line through a GPER-dependent ERα36 induction.. Molecular and Cellular Endocrinology, 2012, 350 (1), pp.61-71. ⟨10.1016/j.mce.2011.11.021⟩. ⟨hal-00746506⟩