Allosteric and Orthosteric Activators of mGluR8 Differentially Affect the Chemotherapeutic‐Induced Human Neuroblastoma SH‐SY5Y Cell Damage: The Impact of Cell Differentiation State. Issue 4 (29th June 2018)

• Record Type: Journal Article
• Authors: Jantas, Danuta; Grygier, Beata; Zatorska, Justyna; Lasoń, Władysław
• Is Part Of: Basic & clinical pharmacology & toxicology. Volume 123:Issue 4(2018)
• Page Start: 443
• Page End: 451
• Publication Date: 2018-06-29
• Subjects: Pharmacology -- Periodicals; Toxicology -- Periodicals; Pharmacology -- Periodicals; Toxicology -- Periodicals; Pharmacology, Clinical -- Periodicals; Computer network resources; Electronic journals; 615.1
• DOI: 10.1111/bcpt.13041
• Languages: English
• ISSNs: 1742-7835

Abstract

Abstract: The participation of group III metabotropic glutamate receptors (mGluRs) in cancer growth and progression is still an understudied issue. Based on our recent data on high expression of mGluR8 in human neuroblastoma SH‐SY5Y cells, in this study, we evaluated the effect of an mGluR8‐specific positive allosteric modulator (PAM: AZ12216052) and orthosteric agonist [(S)‐3, 4‐DCPG ((S)‐3, 4‐dicarboxyphenylglycine)] on chemotherapeutic (doxorubicin, irinotecan or cisplatin)‐evoked cell damage in undifferentiated (UN‐) and retinoic acid‐differentiated (RA‐) SH‐SY5Y cells. The data showed that AZ12216052 as well as a group III mGluR antagonist (UBP1112) but not (S)‐3, 4‐DCPG partially inhibited the cell damage evoked by doxorubicin, irinotecan or cisplatin in UN‐SH‐SY5Y cells. In RA‐SH‐SY5Y, we observed only a modest protective effect of mGluR8 PAM. In contrast, both types of mGluR8 activators significantly enhanced toxic effects of doxorubicin and irinotecan in RA‐SH‐SY5Y cells. These data suggest that in undifferentiated neuroblastoma malignant cells, some mGluR8 modulators can decrease cytotoxic effects of chemotherapeutics which exclude them from the group of putative anticancer agents. On the other hand, in SH‐SY5Y cells differentiated to a more mature neuron‐like phenotype, that is non‐malignant cells, the mGluR8 activators can aggravate the chemotherapeutic neurotoxicity which is a well‐known undesired effect of these drugs. Our pharmacological data add new observations to the unexplored field of research on the role of mGluR8 in cancer, pointing to complexity of response which could be mediated by particular types of mGluR8 ligands at least in neuroblastoma cells.