Artificial and Natural Sweeteners Biased T1R2/T1R3 Taste Receptors Transactivate Glycosylated Receptors on Cancer Cells to Induce Epithelial-Mesenchymal Transition of Metastatic Phenotype

  • Nutrients. 2024 Jun 12;16(12):1840. doi: 10.3390/nu16121840.
Elizabeth Skapinker  1 ,  Rashelle Aldbai  1  2 ,  Emilyn Aucoin  3 ,  Elizabeth Clarke  1 ,  Mira Clark  4 ,  Daniella Ghokasian  1 ,  Haley Kombargi  1 ,  Merlin J Abraham  1 ,  Yunfan Li  4 ,  David A Bunsick  2 ,  Leili Baghaie  2 ,  Myron R Szewczuk  2
Affiliations
  • 1. Faculty of Health Sciences, Queen's University, Kingston, ON K7L 3N9, Canada.
  • 2. Department of Biomedical & Molecular Sciences, Queen's University, Kingston, ON K7L 3N6, Canada.
  • 3. Faculty of Science, Biology (Biomedical Science), York University, Toronto, ON M3J 1P3, Canada.
  • 4. Faculty of Arts and Science, Queen's University, Kingston, ON K7L 3N9, Canada.
PMID: 38931195 DOI: 10.3390/nu16121840
Abstract

Understanding the role of biased taste T1R2/T1R3 G protein-coupled receptors (GPCR) agonists on glycosylated receptor signaling may provide insights into the opposing effects mediated by artificial and natural Sweeteners, particularly in Cancer and metastasis. Sweetener-taste GPCRs can be activated by several active states involving either biased agonism, functional selectivity, or ligand-directed signaling. However, there are increasing arrays of sweetener ligands with different degrees of allosteric biased modulation that can vary dramatically in binding- and signaling-specific manners. Here, emerging evidence proposes the involvement of taste GPCRs in a biased GPCR signaling crosstalk involving matrix metalloproteinase-9 (MMP-9) and neuraminidase-1 (Neu-1) activating glycosylated receptors by modifying sialic acids. The findings revealed that most natural and artificial Sweeteners significantly activate Neu-1 sialidase in a dose-dependent fashion in RAW-Blue and PANC-1 cells. To confirm this biased GPCR signaling crosstalk, BIM-23127 (neuromedin B receptor inhibitor, MMP-9i (specific MMP-9 Inhibitor), and oseltamivir phosphate (specific Neu-1 inhibitor) significantly block sweetener agonist-induced Neu-1 sialidase activity. To assess the effect of artificial and natural Sweeteners on the key survival pathways critical for pancreatic Cancer progression, we analyzed the expression of epithelial-mesenchymal markers, CD24, ADLH-1, E-cadherin, and N-Cadherin in PANC-1 cells, and assess the cellular migration invasiveness in a scratch wound closure assay, and the tunneling nanotubes (TNTs) in staging the migratory intercellular communication. The artificial and natural Sweeteners induced metastatic phenotype of PANC-1 pancreatic Cancer cells to promote migratory intercellular communication and invasion. The Sweeteners also induced the downstream NFκB activation using the secretory Alkaline Phosphatase (SEAP) assay. These findings elucidate a novel taste T1R2/T1R3 GPCR functional selectivity of a signaling platform in which Sweeteners activate downstream signaling, contributing to tumorigenesis and metastasis via a proposed NFκB-induced epigenetic reprogramming modeling.

Keywords
G protein-coupled receptors; T1R2/T1R3; epithelial-mesenchymal transition; glycosylated receptor; migration; pancreatic cancer; sweeteners; tunneling nanotubes.
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