• 3109 Citations
20082021
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Personal profile

Research Interests

Cells in our body can be stimulated to grow and make more cells, such as during normal developmental growth, during the healing of wounds, and upon activation of immune cells in response to pathogens. The Ben-Sahra lab sets out to define the metabolic changes that occur when the signaling pathways are activated both physiologically in normal cells and pathologically in cancer cells. It has emerged recently that many of the genetic factors commonly altered in cancer cells target metabolic genes and especially nucleotide synthesis. Dr. Ben-Sahra’s studies establish important new mechanisms by which growth signals, relayed through the mTOR (mechanistic Target of Rapamycin) pathway, control the synthesis of the two classes of nucleotides, pyrimidines and purines, essential for duplication of our genetic material as DNA during cell division. The Ben-Sahra lab aims to elucidate the molecular mechanisms by which cancer cells use cellular metabolism to promote cell proliferation. Using Mass spectrometry technology, chemical and genetic approaches, we ambition to measure metabolite concentrations and metabolic fluxes in tumorigenic versus non-malignant cells in vitro and in vivo, to systematically identify metabolic states that are sufficient to drive an oncogenic transformation. Elucidating this metabolic interface will provide a mechanistic understanding of tumor initiating events in patients suffering from tumor syndrome or cancer and ultimately lead to new therapeutic strategies to eradicate cancer.

Training Experience

2016Postdoctoral Fellowship, Harvard School of Public Health

Education/Academic qualification

PhD, University of Sophia-Antipolis (Nice, France)

… → 2010

MS, University of Sophia-Antipolis (Nice, France)

… → 2007

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Grants 2017 2021

Epigenomics
Tuberous Sclerosis
Food
Nucleotides
Metabolome
Metabolic Networks and Pathways
Nucleotides
Breast Neoplasms
Phosphatidylinositol 3-Kinases
Oncogenes
Neoplasms
Nucleotides
Carcinogens
Cell Proliferation
RNA

Research Output 2008 2019

  • 3109 Citations
  • 25 Article
  • 5 Review article
  • 3 Short survey

Direct stimulation of NADP + synthesis through Akt-mediated phosphorylation of NAD kinase

Hoxhaj, G., Ben-Sahra, I., Lockwood, S. E., Timson, R. C., Byles, V., Henning, G. T., Gao, P., Selfors, L. M., Asara, J. M. & Manning, B. D., Jan 1 2019, In : Science. 363, 6431, p. 1088-1092 5 p.

Research output: Contribution to journalArticle

NADP
Phosphorylation
NAD
Protein Isoforms
1-Phosphatidylinositol 4-Kinase
2 Citations (Scopus)

Efferocytosis Fuels Requirements of Fatty Acid Oxidation and the Electron Transport Chain to Polarize Macrophages for Tissue Repair

Zhang, S., Weinberg, S., DeBerge, M., Gainullina, A., Schipma, M. J., Kinchen, J. M., Ben-Sahra, I., Gius, D. R., Yvan-Charvet, L., Chandel, N., Schumacker, P. T. & Thorp, E. B., Feb 5 2019, In : Cell Metabolism. 29, 2, p. 443-456.e5

Research output: Contribution to journalArticle

Electron Transport
Fatty Acids
Macrophages
Interleukin-10
NAD

Ex vivo and in vivo stable isotope labelling of central carbon metabolism and related pathways with analysis by LC–MS/MS

Yuan, M., Kremer, D. M., Huang, H., Breitkopf, S. B., Ben-Sahra, I., Manning, B. D., Lyssiotis, C. A. & Asara, J. M., Feb 1 2019, In : Nature Protocols. 14, 2, p. 313-330 18 p.

Research output: Contribution to journalArticle

Isotope Labeling
Glutamine
Metabolism
Isotopes
Labeling
20 Citations (Scopus)

Amino Acid Restriction Triggers Angiogenesis via GCN2/ATF4 Regulation of VEGF and H 2 S Production

Longchamp, A., Mirabella, T., Arduini, A., MacArthur, M. R., Das, A., Treviño-Villarreal, J. H., Hine, C., Ben-Sahra, I., Knudsen, N. H., Brace, L. E., Reynolds, J., Mejia, P., Tao, M., Sharma, G., Wang, R., Corpataux, J. M., Haefliger, J. A., Ahn, K. H., Lee, C. H., Manning, B. D. & 4 othersSinclair, D. A., Chen, C. S., Ozaki, C. K. & Mitchell, J. R., Mar 22 2018, In : Cell. 173, 1, p. 117-129.e14

Research output: Contribution to journalArticle

Vascular Endothelial Growth Factor A
Sulfur Amino Acids
Amino Acids
Endothelial cells
Nutrients

HER2 Signaling Hijacks the Creatine Shuttle to Fuel Breast Cancer Cell Growth

Ben-Sahra, I. & Puissant, A., Dec 4 2018, In : Cell Metabolism. 28, 6, p. 805-807 3 p.

Research output: Contribution to journalShort survey

Creatine
Mitochondrial Form Creatine Kinase
Breast Neoplasms
Growth
Energy Metabolism