Metabolomics and cancer drug discovery: let the cells do the talking

被引:23
作者
D'Alessandro, Angelo [1 ]
Zolla, Lello [1 ]
机构
[1] Univ Tuscia, Dept Ecol & Biol Sci, I-01100 Viterbo, Italy
关键词
SYSTEMS BIOLOGY; KREBS CYCLE; GLYCOLYSIS; METABOLISM; PROTEOMICS; GENOMICS;
D O I
10.1016/j.drudis.2011.09.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recent developments in cancer research have led to reconsiderations regarding metabolic dysfunctions in cancer cell proliferation and differentiation. The original concept stemmed from the observation that, even in presence of oxygen, highly proliferating cells tend to generate energy strictly from the glycolytic pathway, through a process called aerobic glycolysis, also known as the Warburg effect. More recently, advances in the field of metabolomics applied to cancer research enabled the documenting of the generality of the Warburg effect in a broad variety of tumors. Through metabolomics, cancer cells told us that oxidative stress, while representing one leading cause of genetic instability underpinning carcinogenesis, could also deliver a window of probable therapeutic opportunities that is worth opening.
引用
收藏
页码:3 / 9
页数:7
相关论文
共 33 条
  • [1] Bertram John S., 2000, Molecular Aspects of Medicine, V21, P167, DOI 10.1016/S0098-2997(00)00007-8
  • [2] BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
  • [3] DESIGN OF GLYCOLYSIS
    BOITEUX, A
    HESS, B
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1981, 293 (1063) : 5 - 22
  • [4] Cross-Platform Comparison of Methods for Quantitative Metabolomics of Primary Metabolism
    Buescher, Joerg Martin
    Czernik, Dominika
    Ewald, Jennifer Christina
    Sauer, Uwe
    Zamboni, Nicola
    [J]. ANALYTICAL CHEMISTRY, 2009, 81 (06) : 2135 - 2143
  • [5] A Combined Proteomics and Metabolomics Profiling of Gastric Cardia Cancer Reveals Characteristic Dysregulations in Glucose Metabolism
    Cai, Zhen
    Zhao, Jiang-Sha
    Li, Jing-Jing
    Peng, Dan-Ni
    Wang, Xiao-Yan
    Chen, Tian-Lu
    Qiu, Yun-Ping
    Chen, Ping-Ping
    Li, Wen-Jie
    Xu, Li-Yan
    Li, En-Ming
    Tam, Jason P. M.
    Qi, Robert Z.
    Jia, Wei
    Xie, Dong
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (12) : 2617 - 2628
  • [6] Metabolic changes in the glucose-induced apoptotic blastocyst suggest alterations in mitochondrial physiology
    Chi, MMY
    Hoehn, A
    Moley, KH
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 283 (02): : E226 - E232
  • [7] D'Alessandro A., J PROTEOMICS, DOI [10.1016/Jprot2011.01.001, DOI 10.1016/JPROT2011.01.001]
  • [8] Docosohaexanoic acid-supplemented PACA44 cell lines and over-activation of Krebs cycle: An integrated proteomic, metabolomic and interactomic overview
    D'Alessandro, Angelo
    D'Amici, Gian Maria
    Timperio, Anna Maria
    Merendino, Nicolo
    Zolla, Lello
    [J]. JOURNAL OF PROTEOMICS, 2011, 74 (10) : 2138 - 2158
  • [9] A robust high resolution reversed-phase HPLC strategy to investigate various metabolic species in different biological models
    D'Alessandro, Angelo
    Gevi, Federica
    Zolla, Lello
    [J]. MOLECULAR BIOSYSTEMS, 2011, 7 (04) : 1024 - 1032
  • [10] Pharmacoproteomics: a chess game on a protein field
    D'Alessandro, Angelo
    Zolla, Lello
    [J]. DRUG DISCOVERY TODAY, 2010, 15 (23-24) : 1015 - 1023