How does cancer cell metabolism affect tumor migration and invasion?

被引:163
作者
Han, Tianyu [1 ]
Kang, De [1 ]
Ji, Daokun [1 ]
Wang, Xiaoyu [1 ]
Zhan, Weihua [1 ]
Fu, Mingui [1 ]
Xin, Hong-Bo [1 ]
Wang, Jian-Bin [1 ]
机构
[1] Nanchang Univ, Inst Translat Med, Nanchang, Jiangxi, Peoples R China
关键词
cancer cell metabolism; cell migration; metastasis; glycolysis; glutamine; AUTOCRINE MOTILITY FACTOR; KINASE TYPE M2; NF-KAPPA-B; MESENCHYMAL TRANSITION; AEROBIC GLYCOLYSIS; ENERGY-METABOLISM; FUMARATE-HYDRATASE; GLIOMA MIGRATION; EXTRACELLULAR PH; PATIENT SURVIVAL;
D O I
10.4161/cam.26345
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cancer metastasis is the major cause of cancer-associated death. Accordingly, identification of the regulatory mechanisms that control whether or not tumor cells become "directed walkers" is a crucial issue of cancer research. The deregulation of cell migration during cancer progression determines the capacity of tumor cells to escape from the primary tumors and invade adjacent tissues to finally form metastases. The ability to switch from a predominantly oxidative metabolism to glycolysis and the production of lactate even when oxygen is plentiful is a key characteristic of cancer cells. This metabolic switch, known as the Warburg effect, was first described in 1920s, and affected not only tumor cell growth but also tumor cell migration. In this review, we will focus on the recent studies on how cancer cell metabolism affects tumor cell migration and invasion. Understanding the new aspects on molecular mechanisms and signaling pathways controlling tumor cell migration is critical for development of therapeutic strategies for cancer patients.
引用
收藏
页码:395 / 403
页数:9
相关论文
共 111 条
[1]   GLUCOSE-6-PHOSPHATE ISOMERASE [J].
ACHARI, A ;
MARSHALL, SE ;
MUIRHEAD, H ;
PALMIERI, RH ;
NOLTMANN, EA .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1981, 293 (1063) :145-157
[2]   Phosphoglucose Isomerase/Autocrine Motility Factor Mediates Epithelial-Mesenchymal Transition Regulated by miR-200 in Breast Cancer Cells [J].
Ahmad, Aamir ;
Aboukameel, Amro ;
Kong, Dejuan ;
Wang, Zhiwei ;
Sethi, Seema ;
Chen, Wei ;
Sarkar, Fazlul H. ;
Raz, Avraham .
CANCER RESEARCH, 2011, 71 (09) :3400-3409
[3]   Phosphoglucose Isomerase/Autocrine Motility Factor Promotes Melanoma Cell Migration through ERK Activation Dependent on Autocrine Production of Interleukin-8 [J].
Araki, Kenichiro ;
Shimura, Tatsuo ;
Yajima, Toshiki ;
Tsutsumi, Soichi ;
Suzuki, Hideki ;
Okada, Kohji ;
Kobayashi, Tsutomu ;
Raz, Avraham ;
Kuwano, Hiroyuki .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (47) :32305-32311
[4]   The role of versican isoforms V0/V1 in glioma migration mediated by transforming growth factor-β2 [J].
Arslan, F. ;
Bosserhoff, A-K ;
Nickl-Jockschat, T. ;
Doerfelt, A. ;
Bogdahn, U. ;
Hau, P. .
BRITISH JOURNAL OF CANCER, 2007, 96 (10) :1560-1568
[5]   Hypoxia-induced dedifferentiation of tumor cells -: A mechanism behind heterogeneity and aggressiveness of solid tumors [J].
Axelson, H ;
Fredlund, E ;
Ovenberger, M ;
Landberg, G ;
Påhlman, S .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (4-5) :554-563
[6]  
Bartrons R, 2007, J BIOENERG BIOMEMBR, V39, P223, DOI [10.1007/s10863-007-9080-3, 10.1007/S10863-007-9080-3]
[7]   Lactate promotes glioma migration by TGF-β2-dependent regulation of matrix metalloproteinase-2 [J].
Baumann, Fusun ;
Leukel, Petra ;
Doerfelt, Anett ;
Beier, Christoph P. ;
Dettmer, Katja ;
Oefner, Peter J. ;
Kastenberger, Michael ;
Kreutz, Marina ;
Nickl-Jockschat, Thomas ;
Bogdahn, Ulrich ;
Bosserhoff, Anja-Katrin ;
Hau, Peter .
NEURO-ONCOLOGY, 2009, 11 (04) :368-380
[8]  
Brahimi-Horn Christiane, 2006, Bull Cancer, V93, pE73
[9]   Pyruvate uptake is increased in highly invasive ovarian cancer cells under anoikis conditions for anaplerosis, mitochondrial function, and migration [J].
Caneba, Christine A. ;
Bellance, Nadege ;
Yang, Lifeng ;
Pabst, Lisa ;
Nagrath, Deepak .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2012, 303 (08) :E1036-E1052
[10]   Dissemination and growth of cancer cells in metastatic sites [J].
Chambers, AF ;
Groom, AC ;
MacDonald, IC .
NATURE REVIEWS CANCER, 2002, 2 (08) :563-572