Glucose Metabolism in the Progression of Prostate Cancer

被引:108
作者
Cutruzzola, Francesca [1 ]
Giardina, Giorgio [1 ]
Marani, Marina [1 ]
Macone, Alberto [1 ]
Paiardini, Alessandro [2 ]
Rinaldo, Serena [1 ]
Paone, Alessio [1 ]
机构
[1] Sapienza Univ Rome, Dept Biochem Sci A Rossi Fanelli, Rome, Italy
[2] Sapienza Univ Roma, Dept Biol & Biotechnol Charles Darwin, Rome, Italy
关键词
prostate cancer; metabolism; microenvironment; Warburg effect; inflammation; BONE-MARROW; MITOCHONDRIAL ACONITASE; TUMOR-GROWTH; ZINC UPTAKE; KAPPA-B; CELLS; INFLAMMATION; ADIPOSE; ACID; FIBROBLASTS;
D O I
10.3389/fphys.2017.00097
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Prostate cancer is one of the most common types of cancer in western country males but the mechanisms involved in the transformation processes have not been clearly elucidated. Alteration in cellular metabolism in cancer cells is recognized as a hallmark of malignant transformation, although it is becoming clear that the biological features of metabolic reprogramming not only differ in different cancers, but also among different cells in a type of cancer. Normal prostate epithelial cells have a peculiar and very inefficient energy metabolism as they use glucose to synthesize citrate that is secreted as part of the seminal liquid. During the transformation process, prostate cancer cells modify their energy metabolism from inefficient to highly efficient, often taking advantage of the interaction with other cell types in the tumor microenvironment that are corrupted to produce and secrete metabolic intermediates used by cancer cells in catabolic and anabolic processes. We recapitulate the metabolic transformations occurring in the prostate from the normal cell to the metastasis, highlighting the role of the microenvironment and summarizing what is known on the molecular mechanisms involved in the process.
引用
收藏
页数:8
相关论文
共 50 条
[11]   Direct effect of zinc on mitochondrial apoptogenesis in prostate cells [J].
Feng, P ;
Li, TL ;
Guan, ZX ;
Franklin, RB ;
Costello, LC .
PROSTATE, 2002, 52 (04) :311-318
[12]   Reciprocal Metabolic Reprogramming through Lactate Shuttle Coordinately Influences Tumor-Stroma Interplay [J].
Fiaschi, Tania ;
Marini, Alberto ;
Giannoni, Elisa ;
Taddei, Maria Letizia ;
Gandellini, Paolo ;
De Donatis, Alina ;
Lanciotti, Michele ;
Serni, Sergio ;
Cirri, Paolo ;
Chiarugi, Paola .
CANCER RESEARCH, 2012, 72 (19) :5130-5140
[13]   Human ZIP1 is a major zinc uptake transporter for the accumulation of zinc in prostate cells [J].
Franklin, RB ;
Ma, J ;
Zou, J ;
Guan, Z ;
Kukoyi, BI ;
Feng, P ;
Costello, LC .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2003, 96 (2-3) :435-442
[14]  
Franklin Renty B., 2006, BMC Biochemistry, V7, DOI 10.1186/1471-2091-7-10
[15]   Targeting stromal-induced pyruvate kinase M2 nuclear translocation impairs OXPHOS and prostate cancer metastatic spread [J].
Giannoni, Elisa ;
Taddei, Maria Letizia ;
Morandi, Andrea ;
Comito, Giuseppina ;
Calvani, Maura ;
Bianchini, Francesca ;
Richichi, Barbara ;
Raugei, Giovanni ;
Wong, Nicholas ;
Tang, Damu ;
Chiarugi, Paola .
ONCOTARGET, 2015, 6 (27) :24061-24074
[16]   The proton-linked monocarboxylate transporter (MCT) family: structure, function and regulation [J].
Halestrap, AP ;
Price, NT .
BIOCHEMICAL JOURNAL, 1999, 343 :281-299
[17]   Bone marrow fat: linking adipocyte-induced inflammation with skeletal metastases [J].
Hardaway, Aimalie L. ;
Herroon, Mackenzie K. ;
Rajagurubandara, Erandi ;
Podgorski, Izabela .
CANCER AND METASTASIS REVIEWS, 2014, 33 (2-3) :527-543
[18]   Bone marrow adipocytes promote tumor growth in bone via FABP4-dependent mechanisms [J].
Herroon, Mackenzie K. ;
Rajagurubandara, Erandi ;
Hardaway, Aimalie L. ;
Powell, Katelyn ;
Turchick, Audrey ;
Feldmann, Daniel ;
Podgorski, Izabela .
ONCOTARGET, 2013, 4 (11) :2108-2123
[19]   Decreased intracellular zinc in human tumorigenic prostate epithelial cells: a possible role in prostate cancer progression [J].
Huang, Liping ;
Kirschke, Catherine P. ;
Zhang, Yunfan .
CANCER CELL INTERNATIONAL, 2006, 6 (1)
[20]  
Jemal A, 2009, CA-CANCER J CLIN, V59, P225, DOI [10.3322/caac.20006, 10.3322/caac.21254, 10.3322/caac.21332, 10.3322/caac.21551, 10.3322/caac.20073, 10.3322/caac.21387, 10.3322/caac.21654, 10.3322/caac.21601]