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Inositol Phosphate Recycling Regulates Glycolytic and Lipid Metabolism That Drives Cancer Aggressiveness

[Image: see text] Cancer cells possess fundamentally altered metabolism that supports their pathogenic features, which includes a heightened reliance on aerobic glycolysis to provide precursors for synthesis of biomass. We show here that inositol polyphosphate phosphatase 1 (INPP1) is highly express...

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Detalles Bibliográficos
Autores principales: Benjamin, Daniel I., Louie, Sharon M., Mulvihill, Melinda M., Kohnz, Rebecca A., Li, Daniel S., Chan, Lauryn G., Sorrentino, Antonio, Bandyopadhyay, Sourav, Cozzo, Alyssa, Ohiri, Anayo, Goga, Andrei, Ng, Shu-Wing, Nomura, Daniel K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076040/
https://www.ncbi.nlm.nih.gov/pubmed/24738946
http://dx.doi.org/10.1021/cb5001907
Descripción
Sumario:[Image: see text] Cancer cells possess fundamentally altered metabolism that supports their pathogenic features, which includes a heightened reliance on aerobic glycolysis to provide precursors for synthesis of biomass. We show here that inositol polyphosphate phosphatase 1 (INPP1) is highly expressed in aggressive human cancer cells and primary high-grade human tumors. Inactivation of INPP1 leads to a reduction in glycolytic intermediates that feed into the synthesis of the oncogenic signaling lipid lysophosphatidic acid (LPA), which in turn impairs LPA signaling and further attenuates glycolytic metabolism in a feed-forward mechanism to impair cancer cell motility, invasiveness, and tumorigenicity. Taken together these findings reveal a novel mode of glycolytic control in cancer cells that can serve to promote key oncogenic lipid signaling pathways that drive cancer pathogenicity.