4.5 Article

Novel genes involved in pathophysiology of gonadotropin-dependent adrenal tumors in mice

Journal

MOLECULAR AND CELLULAR ENDOCRINOLOGY
Volume 444, Issue C, Pages 9-18

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2017.01.036

Keywords

Adrenal tumor; Pathophysiology; Gonadotropin; GATA4; LHCGR; Biomarker

Funding

  1. Turku Doctoral Programme of Molecular Medicine
  2. Academy of Finland
  3. Sigrid Juselius Foundation
  4. ERVA grant from Turku University Hospital
  5. Turku University Foundation
  6. Polish National Science Center [2015/17/B/N25/00636]

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Specific inbred strains and transgenic inhibin-a Simian Virus 40 T antigen (inhafrag) mice are genetically susceptible to gonadectomy-induced adrenocortical neoplasias. We identified altered gene expression in prepubertally gonadectomized (COX) inh alpha/Tag and wild-type (WT) mice. Besides earlier reported Gata4 and Lhcgr, we found up-regulated Esrl, Prlr-rsl, and down-regulated GrblO, Mrnp24, Sgcd, Rerg, Gnas, Nfatc2, Gnrhr, lgf2 in inh alpha/Tag adrenal tumors. Sex-steroidogenic enzyme genes expression (Srd5a 1, Cypl9a1) was up-regulated in tumors, but adrenal-specific steroidogenic enzyme (Cyp21al, Cyp11b1, Cypl1b2) down-regulated. We localized novel Lhcgr transcripts in adrenal cortex parenchyma and in non-steroidogenic A cells, in GDX WT and in intact WT mice. We identified up-regulated Esr1 as a potential novel biomarker of gonadectomy-induced adrenocortical tumors in inh alpha/fag mice presenting with an inverted adrenal-to-gonadal steroidogenic gene expression profile. A putative normal adrenal remodeling or tumor suppressor role of the down-regulated genes (e.g. Grb 10, Rerg, Gnas, and Nfatc2) in the tumors remains to be addressed. (C) 2017 Elsevier B.V. All rights reserved.

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