miRNA in tumour metabolism and why could it be the preferred pathway for energy reprograming

被引:33
作者
Alamoudi, Aliaa A. [1 ]
Alnoury, Amina [1 ]
Gad, Hoda [1 ]
机构
[1] King Abdulaziz Univ, Dept Clin Biochem, POB 80200, Jeddah 21589, Saudi Arabia
关键词
miRNA; tumour metabolism; Warburg effect; AMPK; exosomes; stemness; CANCER STEM-CELLS; GLUCOSE-TRANSPORTER ISOFORMS; BREAST-CANCER; AEROBIC GLYCOLYSIS; LIPID-METABOLISM; GLUT1; EXPRESSION; MESSENGER-RNAS; IMMUNE CELLS; HEXOKINASE; LUNG-CANCER;
D O I
10.1093/bfgp/elx023
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The current literature on the role of microRNA (miRNA) in tumour metabolism is growing, and a number of studies regularly confirm the impact miRNA can have in energy reprograming in tumours. However, there remains to be a lack of understanding of the larger perspective of the role of miRNA in the metabolism story. In the first part of this review, we provide a comprehensive and up-to-date description of the extensive role of miRNAs in tumour metabolism including glucose, lipid and amino acid metabolism. However, in the second part, we aim to provide a description of the multidimensional role miRNA can be playing in tumour metabolism. Of paramount importance is the role miRNA has in responding to metabolic cues and how it can alter cellular state and fate, including cancer stem cells, in response to such cues. In addition, exosomal miRNAs can provide means by which cells can communicate metabolic signals and messages with other cells within the tumour microenvironment, altering therefore the phenotype and functional capacity of these cells. With this expanding area of research better understanding of the role of miRNA in tumour metabolism in a mechanistic approach, and not only describing which miRNAs can effect which genes, can help to exploit the therapeutic implications behind the extensive role of miRNA in tumour metabolism.
引用
收藏
页码:157 / 169
页数:13
相关论文
共 135 条
[91]   Exosomes released by chronic lymphocytic leukemia cells induce the transition of stromal cells into cancer-associated fibroblasts [J].
Paggetti, Jerome ;
Haderk, Franziska ;
Seiffert, Martina ;
Janji, Bassam ;
Distler, Ute ;
Ammerlaan, Wim ;
Kim, Yeoun Jin ;
Adam, Julien ;
Lichter, Peter ;
Solary, Eric ;
Berchem, Guy ;
Moussay, Etienne .
BLOOD, 2015, 126 (09) :1106-1117
[92]   Warburg Meets Autophagy: Cancer-Associated Fibroblasts Accelerate Tumor Growth and Metastasis via Oxidative Stress, Mitophagy, and Aerobic Glycolysis [J].
Pavlides, Stephanos ;
Vera, Iset ;
Gandara, Ricardo ;
Sneddon, Sharon ;
Pestell, Richard G. ;
Mercier, Isabelle ;
Martinez-Outschoorn, Ubaldo E. ;
Whitaker-Menezes, Diana ;
Howell, Anthony ;
Sotgia, Federica ;
Lisanti, Michael P. .
ANTIOXIDANTS & REDOX SIGNALING, 2012, 16 (11) :1264-1284
[93]   miR-143 regulates hexokinase 2 expression in cancer cells [J].
Peschiaroli, A. ;
Giacobbe, A. ;
Formosa, A. ;
Markert, E. K. ;
Bongiorno-Borbone, L. ;
Levine, A. J. ;
Candi, E. ;
D'Alessandro, A. ;
Zolla, L. ;
Agro, A. Finazzi ;
Melino, G. .
ONCOGENE, 2013, 32 (06) :797-802
[94]   Proline metabolism and cancer: emerging links to glutamine and collagen [J].
Phang, James M. ;
Liu, Wei ;
Hancock, Chad N. ;
Fischer, Joseph W. .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2015, 18 (01) :71-77
[95]   miR-210 is overexpressed in late stages of lung cancer and mediates mitochondrial alterations associated with modulation of HIF-1 activity [J].
Puissegur, M-P ;
Mazure, N. M. ;
Bertero, T. ;
Pradelli, L. ;
Grosso, S. ;
Robbe-Sermesant, K. ;
Maurin, T. ;
Lebrigand, K. ;
Cardinaud, B. ;
Hofman, V. ;
Fourre, S. ;
Magnone, V. ;
Ricci, J. E. ;
Pouyssegur, J. ;
Gounon, P. ;
Hofman, P. ;
Barbry, P. ;
Mari, B. .
CELL DEATH AND DIFFERENTIATION, 2011, 18 (03) :465-478
[96]   miR-29a and miR-29b Contribute to Pancreatic β-Cell-Specific Silencing of Monocarboxylate Transporter 1 (Mct1) [J].
Pullen, Timothy J. ;
Xavier, Gabriela da Silva ;
Kelsey, Gavin ;
Rutter, Guy A. .
MOLECULAR AND CELLULAR BIOLOGY, 2011, 31 (15) :3182-3194
[97]   Glut1 and Glut3 as Potential Prognostic Markers for Oral Squamous Cell Carcinoma [J].
Rojas Ayala, Fernanda Rocha ;
Rocha, Rafael Malagoli ;
Carvalho, Katia Candido ;
Carvalho, Andre Lopes ;
da Cunha, Isabela Werneck ;
Lourenco, Silvia Vanessa ;
Soares, Fernando Augusto .
MOLECULES, 2010, 15 (04) :2374-2387
[98]   Bladder Cancer-Associated Gene Expression Signatures Identified by Profiling of Exfoliated Urothelia [J].
Rosser, Charles J. ;
Liu, Li ;
Sun, Yijun ;
Villicana, Patrick ;
McCullers, Molly ;
Porvasnik, Stacy ;
Young, Paul R. ;
Parker, Alexander S. ;
Goodison, Steve .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2009, 18 (02) :444-453
[99]   MicroRNA let-7a down-regulates MYC and reverts MYC-induced growth in Burkitt lymphoma cells [J].
Sampson, Valerie B. ;
Rong, Nancy H. ;
Han, Jian ;
Yang, Qunying ;
Aris, Virginie ;
Soteropoulos, Patricia ;
Petrelli, Nicholas J. ;
Dunn, Stephen P. ;
Krueger, Leslie J. .
CANCER RESEARCH, 2007, 67 (20) :9762-9770
[100]   Hallmarks of cancer stem cell metabolism [J].
Sancho, Patricia ;
Barneda, David ;
Heeschen, Christopher .
BRITISH JOURNAL OF CANCER, 2016, 114 (12) :1305-1312