Literature DB >> 22070544

Integration of metabolomics and expression of glycerol-3-phosphate acyltransferase (GPAM) in breast cancer-link to patient survival, hormone receptor status, and metabolic profiling.

Scarlet F Brockmöller1, Elmar Bucher, Berit M Müller, Jan Budczies, Mika Hilvo, Julian L Griffin, Matej Orešič, Olli Kallioniemi, Kristiina Iljin, Sibylle Loibl, Silvia Darb-Esfahani, Bruno V Sinn, Frederick Klauschen, Judith Prinzler, Nikola Bangemann, Fakher Ismaeel, Oliver Fiehn, Manfred Dietel, Carsten Denkert.   

Abstract

Changes in lipid metabolism are an important but not well-characterized hallmark of cancer. On the basis of our recent findings of lipidomic changes in breast cancer, we investigated glycerol-3-phosphate acyltransferase (GPAM), a key enzyme in the lipid biosynthesis of triacylglycerols and phospholipids. GPAM protein expression was evaluated and linked to metabolomic and lipidomic profiles in a cohort of human breast carcinomas. In addition, GPAM mRNA expression was analyzed using the GeneSapiens in silico transcriptiomics database. High cytoplasmic GPAM expression was associated with hormone receptor negative status (p = 0.013). On the protein (p = 0.048) and mRNA (p = 0.001) levels, increased GPAM expression was associated with a better overall survival. Metabolomic analysis by GC-MS showed that sn-glycerol-3-phosphate, the substrate of GPAM, was elevated in breast cancer compared to normal breast tissue. LC-MS based lipidomic analysis identified significantly higher levels of phospholipids, especially phosphatidylcholines in GPAM protein positive tumors. In conclusion, our results suggest that GPAM is expressed in human breast cancer with associated changes in the cellular metabolism, in particular an increased synthesis of phospholipids, the major structural component of cellular membranes.

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Year:  2011        PMID: 22070544     DOI: 10.1021/pr200685r

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  29 in total

Review 1.  Review of mass spectrometry-based metabolomics in cancer research.

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3.  Impact of tumor microenvironment and epithelial phenotypes on metabolism in breast cancer.

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Journal:  Clin Cancer Res       Date:  2012-12-12       Impact factor: 12.531

4.  Aquaporin-7 Regulates the Response to Cellular Stress in Breast Cancer.

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Journal:  Cancer Res       Date:  2020-07-06       Impact factor: 12.701

5.  Analysis of miRNA-seq in the liver of common carp (Cyprinus carpio L.) in response to different environmental temperatures.

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6.  Disruption of tumor suppressor gene Hint1 leads to remodeling of the lipid metabolic phenotype of mouse liver.

Authors:  Diren Beyoğlu; Kristopher W Krausz; Juliette Martin; Olivier Maurhofer; Juliane Dorow; Uta Ceglarek; Frank J Gonzalez; Jean-François Dufour; Jeffrey R Idle
Journal:  J Lipid Res       Date:  2014-09-05       Impact factor: 5.922

7.  Metabolomics of human breast cancer: new approaches for tumor typing and biomarker discovery.

Authors:  Carsten Denkert; Elmar Bucher; Mika Hilvo; Reza Salek; Matej Orešič; Julian Griffin; Scarlet Brockmöller; Frederick Klauschen; Sibylle Loibl; Dinesh Kumar Barupal; Jan Budczies; Kristiina Iljin; Valentina Nekljudova; Oliver Fiehn
Journal:  Genome Med       Date:  2012-04-30       Impact factor: 11.117

8.  Metabolic Signatures of Human Breast Cancer.

Authors:  Prachi Mishra; Stefan Ambs
Journal:  Mol Cell Oncol       Date:  2015 Jul-Sep

Review 9.  A rough guide to metabolite identification using high resolution liquid chromatography mass spectrometry in metabolomic profiling in metazoans.

Authors:  David G Watson
Journal:  Comput Struct Biotechnol J       Date:  2013-02-15       Impact factor: 7.271

10.  Integrated analysis of transcript-level regulation of metabolism reveals disease-relevant nodes of the human metabolic network.

Authors:  Mafalda Galhardo; Lasse Sinkkonen; Philipp Berninger; Jake Lin; Thomas Sauter; Merja Heinäniemi
Journal:  Nucleic Acids Res       Date:  2013-11-05       Impact factor: 16.971

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