Identification of K.sub.Ca3.1 Channel as a Novel Regulator of Oxidative Phosphorylation in a Subset of Pancreatic Carcinoma Cell Lines

• Published in: PloS one Vol. 11; no. 8; p. e0160658
• Main Authors: Kovalenko, Ilya, Glasauer, Andrea, Schöckel, Laura, Sauter, Daniel R. P, Ehrmann, Alexander, Sohler, Florian, Hägebarth, Andrea, Novak, Ivana, Christian, Sven
• Format: Journal Article
• Language: English
• Published: Public Library of Science 05.08.2016
• Subjects: Care and treatment; Cell metabolism; Genetic aspects; Oxidative phosphorylation; Pancreatic cancer; Risk factors; United States
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0160658

Pancreatic ductal adenocarcinoma (PDAC) represents the most common form of pancreatic cancer with rising incidence in developing countries and overall 5-year survival rates of less than 5%. The most frequent mutations in PDAC are gain-of-function mutations in KRAS as well as loss-of-function mutations in p53. Both mutations have severe impacts on the metabolism of tumor cells. Many of these metabolic changes are mediated by transporters or channels that regulate the exchange of metabolites and ions between the intracellular compartment and the tumor microenvironment. In the study presented here, our goal was to identify novel transporters or channels that regulate oxidative phosphorylation (OxPhos) in PDAC in order to characterize novel potential drug targets for the treatment of these cancers. We set up a Seahorse Analyzer XF based siRNA screen and identified previously described as well as novel regulators of OxPhos. The siRNA that resulted in the greatest change in cellular oxygen consumption was targeting the KCNN4 gene, which encodes for the Ca.sup.2+ -sensitive K.sup.+ channel K.sub.Ca 3.1. This channel has not previously been reported to regulate OxPhos. Knock-down experiments as well as the use of a small molecule inhibitor confirmed its role in regulating oxygen consumption, ATP production and cellular proliferation. Furthermore, PDAC cell lines sensitive to K.sub.Ca 3.1 inhibition were shown to express the channel protein in the plasma membrane as well as in the mitochondria. These differences in the localization of K.sub.Ca 3.1 channels as well as differences in the regulation of cellular metabolism might offer opportunities for targeted therapy in subsets of PDAC.