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

被引:46
作者
Benjamin, Daniel I. [1 ]
Louie, Sharon M. [1 ]
Mulvihill, Melinda M. [1 ]
Kohnz, Rebecca A. [1 ]
Li, Daniel S. [1 ]
Chan, Lauryn G. [1 ]
Sorrentino, Antonio [3 ]
Bandyopadhyay, Sourav [4 ]
Cozzo, Alyssa [1 ]
Ohiri, Anayo [1 ]
Goga, Andrei [2 ,3 ,4 ]
Ng, Shu-Wing [5 ]
Nomura, Daniel K. [1 ]
机构
[1] Univ Calif Berkeley, Dept Nutr Sci & Toxicol, Program Metab Biol, Berkeley, CA 94720 USA
[2] Univ Calif San Francisco, Dept Cell & Tissue Biol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Div Hematol Oncol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, San Francisco Helen Diller Family Comprehens Canc, San Francisco, CA 94143 USA
[5] Harvard Univ, Sch Med, Brigham & Womens Hosp, Lab Gynecol Oncol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
POLYPHOSPHATE; 1-PHOSPHATASE; LYSOPHOSPHATIDIC ACID; PROSTATE-CANCER; PATHWAYS; BRAIN; METASTASIS; INHIBITOR; GROWTH; ENZYME; CELLS;
D O I
10.1021/cb5001907
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:1340 / 1350
页数:11
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