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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