Anti-proliferative and anti-secretory effects of everolimus on human pancreatic neuroendocrine tumors primary cultures: is there any benefit from combination with somatostatin analogs?

Amira Mohamed (1) , David Romano (2) , Alexandru Saveanu (2) , Catherine Roche (1) , Manuela Albertelli (3) , Federica Barbieri (3) , Thierry Brue (1) , Patricia Niccoli (4) , Jean-Robert Delpero (5) , Stéphane Garcia (6) , Diego Ferone (3) , Tullio Florio (3) , Vincent Moutardier (7) , Flora Poizat (8) , Anne A. Barlier (1) , Corinne Gerard (1)

1 CRN2M - Centre de recherche en neurobiologie - neurophysiologie de Marseille
2 ICN - Interactions cellulaires neuroendocriniennes
3 UniGe - Università degli studi di Genova = University of Genoa
4 TIMONE - Hôpital de la Timone [CHU - APHM]
5 Department of Surgical Oncology
6 Hôpital Nord [CHU - APHM]
7 AMU MED - Aix-Marseille Université - Faculté de médecine
8 Institut Paoli-Calmettes

Therapeutic management of gastroenteropancreatic neuroendocrine tumors (GEP-NETs) is challenging. The mammalian target of rapamycin (mTOR) inhibitor everolimus recently obtained approval from the Food and Drug Administration for the treatment of patients with advanced pancreatic neuroendocrine tumors (pNETs). Despite its promising antitumor efficacy observed in cell lines, clinical benefit for patients is unsatisfactory. The limited therapeutic potential of everolimus in cancer cells has been attributed to Akt activation due to feedback loops relief following mTOR inhibition. Combined inhibition of Akt might then improve everolimus antitumoral effect. In this regard, the somatostatin analog (SSA) octreotide has been shown to repress the PI3K/ Akt pathway in some tumor cell lines. Moreover, SSAs are well tolerated and routinely used to reduce symptoms caused by peptide release in patients carrying functional GEP-NETs. We have recently established and characterized primary cultures of human pNETs and demonstrated the anti-proliferative effects of both octreotide and pasireotide. In this study, we aim at determining the antitumor efficacy of everolimus alone or in combination with the SSAs octreotide and pasireotide in primary cultures of pNETs. Everolimus reduced both Chromogranin A secretion and cell viability and upregulated Akt activity in single treatment. Its anti-proliferative and anti-secretory efficacy was not improved combined with the SSAs. Both SSAs did not overcome everolimus-induced Akt upregulation. Furthermore, caspase-dependent apoptosis induced by SSAs was lost in combined treatments. These molecular events provide the first evidence supporting the lack of marked benefit in patients co-treated with everolimus and SSA. www.impactjournals.com/oncotarget/

Keywords: co-treatment; everolimus; somatostatin analogs; primary culture; human pancreatic neuroendocrine tumors

Domains: Life Sciences [q-bio]; Pharmaceutical sciences; Pharmacology; Life Sciences [q-bio]; Cancer; Life Sciences [q-bio]; Human health and pathology; Hépatology and Gastroenterology

Amira Mohamed, David Romano, Alexandru Saveanu, Catherine Roche, Manuela Albertelli, et al.. Anti-proliferative and anti-secretory effects of everolimus on human pancreatic neuroendocrine tumors primary cultures: is there any benefit from combination with somatostatin analogs?. Oncotarget, 2017, 8 (25), pp.41044-41063. ⟨10.18632/oncotarget.17008⟩. ⟨hal-01731582⟩