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PMID: 20139083 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Metabolomic changes accompanying transformation and acquisition of metastatic potential in a syngeneic mouse mammary tumor model.

The Journal of biological chemistry ·Vol. 285 ·No. 13 ·2010-03-26 ·Pages 9317-9321

Lu X, Bennet B, Mu E, Rabinowitz J, Kang Y

Abstract

Breast cancer is the most common cancer type for women in the western world. Despite decades of research, the molecular processes associated with breast cancer progression are still inadequately defined. Here, we focus on the systematic alteration of metabolism by using the state of the art metabolomic profiling techniques to investigate the changes of 157 metabolites during the progression of normal mouse mammary epithelial cells to an isogenic series of mammary tumor cell lines with increasing metastatic potentials. Our results suggest a two-step metabolic progression hypothesis during the acquisition of tumorigenic and metastatic abilities. Metabolite changes accompanying tumor progression are identified in the intracellular and secreted forms in several pathways, including glycolysis, the tricarboxylic acid cycle, the pentose phosphate pathway, fatty acid and nucleotide biosynthesis, and the GSH-dependent antioxidative pathway. These results suggest possible biomarkers of breast cancer progression as well as opportunities of interrupting tumor progression through the targeting of metabolic pathways.

MeSH Terms
Animals Biomarkers, Tumor/metabolism Cell Line, Tumor Cell Transformation, Neoplastic Culture Media, Conditioned Disease Progression Epithelial Cells/metabolism Gene Expression Regulation, Neoplastic Glutathione/metabolism Mammary Neoplasms, Animal/metabolism Mammary Tumor Virus, Mouse/metabolism Mice Neoplasm Metastasis
Chemicals
Biomarkers, Tumor Culture Media, Conditioned Glutathione
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Lu Xin
Department of Molecular Biology, New Jersey 08544.
Bennet Bryson
Lewis-Sigler Institute for Integrative Genomics, New Jersey 08544; Department of Chemistry, Princeton University, Princeton, New Jersey 08544.
Mu Euphemia
Department of Molecular Biology, New Jersey 08544.
Rabinowitz Joshua
Lewis-Sigler Institute for Integrative Genomics, New Jersey 08544; Department of Chemistry, Princeton University, Princeton, New Jersey 08544.
Kang Yibin
Department of Molecular Biology, New Jersey 08544; Breast Cancer Program, Cancer Institute of New Jersey, New Brunswick, New Jersey 08903. Electronic address: ykang@princeton.edu.
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Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
1083-351X
Published
2010-03-26
Epub
2010-00-05
Pages
9317-9321
Language
English
Region
United States
NLM ID
2985121R
PMCID
PMC2843179
Subset
IM
Grants
NCI NIH HHS · R01 CA134519 · United States
NCI NIH HHS · R21 CA128620 · United States
NCI NIH HHS · R01CA134519 · United States
NCI NIH HHS · R21CA128620 · United States
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