The glucose and lipid metabolism reprogramming is gradedependent in clear cell renal cell carcinoma primary cultures and is targetable to modulate cell viability and proliferation
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Cristina Bianchi1, Chiara Meregalli1, Silvia Bombelli1, Vitalba Di Stefano1, Francesco Salerno1, Barbara Torsello1, Sofia De Marco1, Giorgio Bovo2,8, Ingrid Cifola3, Eleonora Mangano3, Cristina Battaglia4, Guido Strada5, Giuseppe Lucarelli6, Robert H. Weiss7 and Roberto A. Perego1
1School of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy
2Pathology Unit, ASST Monza, San Gerardo Hospital, Monza, Italy
3Institute for Biomedical Technologies, National Research Council, Segrate, Italy
4Department of Medical Biotechnology and Translational Medicine, University of Milano, Segrate, Italy
5Urology Unit, ASST North Milan, Bassini Hospital, Cinisello Balsamo, Italy
6Department of Emergency and Organ Transplantation-Urology, University of Bari, Bari, Italy
7Division of Nephrology, Department of Internal Medicine, School of Medicine, and Cancer Center, University of California, Davis, CA, USA
8Current address: Pathology Unit, ASST North Milan, Vimercate Hospital, Vimercate, Italy
Roberto A. Perego, email: firstname.lastname@example.org
Keywords: renal cell carcinoma; primary cell cultures; glucose and lipid metabolism reprogramming; Fuhrman grade
Received: July 19, 2017 Accepted: November 14, 2017 Published: December 08, 2017
Clear cell renal cell carcinoma (ccRCC) has a poor prognosis despite novel biological targeted therapies. Tumor aggressiveness and poor survival may correlate with tumor grade at diagnosis and with complex metabolic alterations, also involving glucose and lipid metabolism. However, currently no grade-specific metabolic therapy addresses these alterations. Here we used primary cell cultures from ccRCC of low- and high-grade to investigate the effect on energy state and reduced pyridine nucleotide level, and on viability and proliferation, of specific inhibition of glycolysis with 2-deoxy-D-glucose (2DG), or fatty acid oxidation with Etomoxir. Our primary cultures retained the tissue grade-dependent modulation of lipid and glycogen storage and aerobic glycolysis (Warburg effect). 2DG affected lactate production, energy state and reduced pyridine nucleotide level in high-grade ccRCC cultures, but the energy state only in low-grade. Rather, Etomoxir affected energy state in high-grade and reduced pyridine nucleotide level in low-grade cultures. Energy state and reduced pyridine nucleotide level were evaluated by ATP and reduced 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium (MTT) dye quantification, respectively. 2DG treatment impaired cell proliferation and viability of low-grade ccRCC and normal cortex cultures, whereas Etomoxir showed a cytostatic and cytotoxic effect only in high-grade ccRCC cultures. Our data indicate that in ccRCC the Warburg effect is a grade-dependent feature, and fatty acid oxidation can be activated for different grade-dependent metabolic needs. A possible grade-dependent metabolic therapeutic approach in ccRCC is also highlighted.
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