Searchable abstracts of presentations at key conferences in endocrinology

ea0056oc5.3 | Diving deep into adrenal cortex diseases | ECE2018

PRKACA L206R mutation in adrenal Cushing’s syndrome makes PKA RIIβ susceptible for caspase-mediated cleavage

Weigand Isabel , Ronchi Cristina L. , Hofner Kerstin , Vanselow Jens T. , Herterich Sabine , Bathon Kerstin , Schlosser Andreas , Fassnacht Martin , Calebiro Davide

Protein Kinase A (PKA) consists of two catalytic and two regulatory subunits with several isoforms (Cα, β, γ and RIα, IIα, Iβ, IIβ, respectively). Type II regulatory subunits are phosphorylated by PKA in their inhibitory sites, while type I are not. Somatic activating mutations in the gene encoding the catalytic subunit α (Cα) of PKA (PRKACA) have been found in 30–40% of cortisol-producing adrenocortical adenomas (CPA). We rece...

ea0056gp32 | Adrenal cortex | ECE2018

PRKACA L206R mutation in adrenal Cushing induces histone H1.4 hyper-phosphorylation

Bathon Kerstin , Weigand Isabel , Vanselow Jens T , Ronchi Cristina L , Sbiera Silviu , Schlosser Andreas , Fassnacht Martin , Calebiro Davide

We previously identified mutations in PRKACA, coding for the catalytic a (Ca) subunit of protein kinase A (PKA), as the main genetic alteration in cortisol-producing adrenal adenomas (CPAs) responsible for Cushing’s syndrome. Here, we further investigated the mechanism of action of all PRKACA mutations identified so far by our team (L206R, L199_C200_insW, S213R_L212_K214insIILR, C200_GlyinsV, W197R, del244-248+E249Q and E32V). Five out of seven mutants s...

ea0049gp1 | Adrenal 1 | ECE2017

PRKACA mutations in adrenal Cushing can alter substrate specificity

Bathon Kerstin , Weigand Isabel , Vanselow Jens T , Ronchi Cristina L , Di Dalmazi Guido , Beuschlein Felix , Sbiera Silviu , Schlosser Andreas , Fassnacht Martin , Calebiro Davide

Previously, we identified seven mutations in the main catalytic subunit of protein kinase A (PKA Cα) to be responsible for cortisol-secreting adrenocortical adenomas (CPAs): L206R, L199_C200_insW, S213R_L212_K214insIILR, C200_GlyinsV, W197R, del244-248+E249Q, E32V. Here we performed a functional characterization of these mutants. Specifically, we evaluated the association between PKA regulatory and catalytic subunits using co-immunoprecipitation and PKA activity using a k...

ea0049ep932 | Pituitary - Basic | ECE2017

Ubiquitin specific peptidase 8 (USP8) in human corticotroph pituitary tumors- possible targets and mode of action

Weigand Isabel , Knobloch Lisanne , Vanselow Jens T. , Flitsch Jorg , Monoranu Carmelia M , Saeger Wolfgang , Hagel Christian , Herterich Sabine , Ronchi Cristina , Schlosser Andreas , Fassnacht Martin , Deutschbein Timo , Sbiera Silviu

Recently, somatic, heterozygous mutations in the gene encoding the deubiquitinase USP8 have been identified in 30–60% of corticotroph tumors. These mutations were found to hinder binding of 14-3-3 proteins, increasing its deubiquitinating activity. One substrate is Epidermal Growth Factor Receptor (EGFR), USP8 triggering EGFR recycling and increased EGFR signaling. However, tumors harboring mutations in USP8 are smaller than WT tumors, raising the debate if EGFR, as a pot...

ea0049gp5 | Adrenal 1 | ECE2017

Protein Kinase A signaling saves regulatory subunit IIβ from PRKACA mutation-mediated degradation

Weigand Isabel , Bathon Kerstin , Ronchi Cristina , Rizk-Rabin Marthe , Di Dalmazi Guido , Wild Vanessa , Rubin Beatrice , Vanselow Jens T , Schlosser Andreas , Calebiro Davide , Beuschlein Felix , Bertherat Jerome , Fassnacht Martin , Sbiera Silviu

Protein Kinase A (PKA) consists of two catalytic and two regulatory subunits with several isoforms (Cα,β,γ, RIα,IIα,Iβ,IIβ). In 30–40% of cortisol-producing adrenocortical adenomas (CPA) heterozygous activating somatic mutations in the catalytic subunit α (Cα) of PKA have been found. Previous reports found strikingly reduced levels of RIIβ in CPA compared to other adrenocortical tumors. Here, we investigated the correlatio...

ea0056gp198 | Pituitary Basic | ECE2018

Ubiquitin specific peptidase 8 (USP8) in human corticotroph pituitary tumors- possible targets and mode of action

Weigand Isabel , Knobloch Lisanne , Vanselow Jens T , Flitsch Jorg , Monoranu Camelia Maria , Saeger Wolfgang , Hagel Christian , Herterich Sabine , Ronchi Cristina L , Schosser Andreas , Fassnacht Martin , Deutschbein Timo , Sbiera Silviu

Recently, somatic, heterozygous mutations in the gene encoding the deubiquitinase USP8 have been identified in 30–60% of corticotroph tumors. These mutations were found to hinder binding of 14-3-3 proteins, increasing its deubiquitinating activity. One substrate is Epidermal Growth Factor Receptor (EGFR), USP8 triggers EGFR recycling and increased EGFR signaling. However, tumors harboring mutations in USP8 are smaller than WT tumors, raising the debate if EGFR, as a poten...

ea0037gp.29.01 | Endocrine tumours and neoplasia – Adrenal Tumour | ECE2015

Mitotane inhibits sterol-o-acyltransferase leading to lipid-mediated endoplasmic reticulum stress and apoptosis of adrenocortical carcinoma cells

Sbiera Silviu , Fassnacht Martin , Leich Ellen , Liebisch Gerhard , Schirbel Andreas , Wiemer Laura , Matysik Silke , Vanselow Jens T , Gardill Felix , Gehl Annemarie , Kendl Sabine , Beyer Melanie , Bala Margarita , Ronchi Cristina L , Deutschbein Timo , Schlosser Andreas , Schmitz Gerd , Rosenwald Andreas , Allolio Bruno , Kroiss Matthias

Context: Mitotane is the only drug approved for treatment of adrenocortical carcinoma (ACC) and in clinical use for more than 50 years. Mitotane counteracts both tumour growth and tumoral steroid hormone production but treatment is associated with severe side effects. The molecular mechanism of mitotane is still unknown, which hampers progress in treatment of ACC.Objective: To identify the mechanism of action and molecular target of mitotane.<p class...