Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2016) 41 EP598 | DOI: 10.1530/endoabs.41.EP598

ECE2016 Eposter Presentations Endocrine tumours and neoplasia (68 abstracts)

Norepinephrine transporter (NET) as a predictive marker of response to PI3K/mTOR inhibition in pheochromocytoma

Ninelia Minaskan 1 , Misu Lee 1 , Iina Laitinen 2 , Rickmer Braren 3 & Natalia S Pellegata 1


1Institute of Pathology, Munich, Germany; 2Department of Nuclear Medicine, Klinikum rechts der Isar, Munich, Germany; 3Institute of Radiology, Klinikum rechts der Isar, Munich, Germany.


Phaeochromocytomas (PCs) are neuroendocrine tumors derived from neural crest-derived chromaffin cells of the adrenal medulla and sympathetic ganglia.

About 10% of all PCs can be malignant.

Currently, there is no effective therapy for malignant PCs.

In many neuroendocrine tumors, including PCs, the PI3K/AKT/mTOR survival pathway is hyperactivated. Therefore, the inhibition of this signaling cascade may exert an antitumor effect.

In our study we evaluated the efficacy of a dual PI3K/mTOR inhibitor, BEZ235, against PC in vivo to avoid the re-activation of upstream AKT signaling following mTOR inhibition. We took advantage of a unique in vivo model of endogenous PCs: MENX-effected rats.

Beside antitumor effects of BEZ235 on PCs cells, gene expression analyses of tumors from rats treated with placebo or with BEZ235 identified the Slc6a2 gene, encoding the norepinephrine transporter (NET), as being down-regulated following drug treatment. NET is responsible for the intracellular re-uptake of norepinephrine in chromaffin cells. The fact that NET is expressed by PC cells has been extensively exploited for the functional imaging of these tumors using radiolabeled norepinephrine analogues. We observed a dose-dependent reduction of both Slc6a2 (by TaqMan) and NET (by immunohistochemistry) expression in rat PCs following BEZ235 administration, which associated with decreased uptake of the radiolabeled norepinephrine analogue 18F-LMI1195 in vivo. To assess the relationship between NET levels and response to BEZ235, we generated a drug-resistant derivative of the MPC cell line. While incubation with BEZ235 reduced NET expression in MPC cells, no reduction was observed in the resistant derivative cells, suggesting that decreased NET expression associates with the ability of PC cells to respond to PI3K/mTOR inhibition.

Altogether, our data demonstrate that targeting PI3K/mTOR signalling is effective against PCs and suggest that NET levels may represent a surrogate marker of therapy response to PI3K/mTOR inhibitors, which can be monitored by functional PET imaging.

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