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The hexosamine biosynthetic pathway couples growth factor-induced glutamine uptake to glucose metabolism
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Glucose and glutamine serve as the two primary carbon sources in proliferating cells, and uptake of both nutrients is directed by growth factor signaling. Although either glucose or glutamine can potentially support mitochondrial tricarboxylic acid (TCA) cycle integrity and ATP production, we found that glucose deprivation led to a marked reduction in glutamine uptake and progressive cellular atrophy in multiple mammalian cell types. Despite the continuous presence of growth factor and an abundant supply of extracellular glutamine, interleukin-3 (IL-3)-dependent cells were unable to maintain TCA cycle metabolite pools or receptor-dependent signal transduction when deprived of glucose. This was due at least in part to down-regulation of IL-3 receptor α (IL-3Rα) surface expression in the absence of glucose. Treatment of glucose-starved cells with N-acetylglucosamine (GlcNAc) to maintain hexosamine biosynthesis restored mitochondrial metabolism and cell growth by promoting IL-3-dependent glutamine uptake and metabolism. Thus, glucose metabolism through the hexosamine biosynthetic pathway is required to sustain sufficient growth factor signaling and glutamine uptake to support cell growth and survival.
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“It would also fit with the importance of glucose carbon to be metabolized through other branches of glycolytic metabolism, including serine synthesis (as discussed above) and the hexosamine pathway (Wellen et al., 2010).”
From Metabolic Reprogramming: A Cancer Hallmark Even Warburg Did Not Anticipate (2012) · cites this paper as Wellen et al., 2010
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“But they also collaborate in another biochemical pathway to produce hexosamines, which modify nutrient transporters and growth factor receptors, enabling their expression on the cell membrane (Figure 2).”
From Cellular Metabolism and Disease: What Do Metabolic Outliers Teach Us? (2012) · cites this paper as Wellen et al., 2010
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Guertin, D. A., & Sabatini, D. M. (2007) · Cancer Cell · doi:10.1016/j.ccr.2007.05.008 · Cited by 2,833
DeBerardinis, R. J., Mancuso, A., Daikhin, E., Nissim, I., Yudkoff, M., Wehrli, S., & Thompson, C. B. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709747104 · Cited by 2,622
Self-citationATP-citrate lyase links cellular metabolism to histone acetylation
Wellen, K. E., Hatzivassiliou, G., Sachdeva, U. M., Bui, T. V., Cross, J. R., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1164097 · Cited by 2,298
Self-citationGao, P., Tchernyshyov, I., Chang, T.-C., Lee, Y.-S., Kita, K., Ochi, T., Zeller, K. I., De Marzo, A. M., Van Eyk, J. E., Mendell, J. T., et al. (2009) · Nature · doi:10.1038/nature07823 · Cited by 2,124
Wise, D. R., DeBerardinis, R. J., Mancuso, A., Sayed, N., Zhang, X.-Y., Pfeiffer, H. K., Nissim, I., Daikhin, E., Yudkoff, M., McMahon, S. B., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810199105 · Cited by 2,001
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Itkonen, H. M., Minner, S. J. P., Guldvik, I. J., Sandmann, M. J., Tsourlakis, M. C., Berge, V., Svindland, A., Schlomm, T., & Mills, I. G. (2013) · Cancer Research · doi:10.1158/0008-5472.can-13-0549 · Cited by 306
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Lynch, T. P., Ferrer, C. M., Jackson, S. R., Shahriari, K. S., Vosseller, K., & Reginato, M. J. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.302547 · Cited by 296
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Campbell, S. L., & Wellen, K. E. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.07.015 · Cited by 186
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Colombo, S. L., Palacios‐Callender, M., Frakich, N., Carcamo, S., Kovacs, I., Tudzarova, S., & Moncada, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117500108 · Cited by 171
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Ma, J., Wu, C., & Hart, G. W. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00884 · Cited by 172
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Kuo, J. C., Gandhi, J. G., Zia, R. N., & Paszek, M. J. (2018) · Nature Physics · doi:10.1038/s41567-018-0186-9 · Cited by 165
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Phang, J. M., Liu, W., Hancock, C. N., & Christian, K. J. (2012) · Frontiers in Oncology · doi:10.3389/fonc.2012.00060 · Cited by 164
Huber, A., Lebeau, J., Guillaumot, P., Pétrilli, V., Malek, M., Chilloux, J., Fauvet, F., Payen, L. F., Kfoury, A., Renno, T., et al. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.01.009 · Cited by 169
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Thai, M., Thaker, S. K., Feng, J., Du, Y., Hu, H., Wu, T., Graeber, T. G., Braas, D., & Christofk, H. R. (2015) · Nature Communications · doi:10.1038/ncomms9873 · Cited by 153
Ren, P., Yue, M., Xiao, D., Xiu, R., Gan, L., Liu, H., & Qing, G. (2014) · The Journal of Pathology · doi:10.1002/path.4429 · Cited by 157
Li, H., Zhu, W., Zhang, L., Lei, H., Wu, X., Guo, L., Chen, X., Wang, Y., & Tang, H. (2015) · Scientific Reports · doi:10.1038/srep08421 · Cited by 154
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Hu, C., Fan, L., Cen, P., Chen, E., Jiang, Z., & Li, L. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17020253 · Cited by 143
Robey, R. B., Weisz, J., Kuemmerle, N. B., Salzberg, A. C., Berg, A. S., Brown, D. G., Maurer, L. L., Palorini, R., Al‐Mulla, F., Al-Temaimi, R. A., et al. (2015) · Carcinogenesis · doi:10.1093/carcin/bgv037 · Cited by 143
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Torrino, S., Grasset, E. M., Audebert, S., Belhadj, I., Lacoux, C., Haynes, M., Pisano, S., Abélanet, S., Brau, F., Chan, S. Y., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.05.009 · Cited by 145
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Still, E. R., & Yuneva, M. O. (2017) · British Journal of Cancer · doi:10.1038/bjc.2017.113 · Cited by 142
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Sommermann, T. G., O’Neill, K. E., Plas, D. R., & Cahir-McFarland, E. D. (2011) · Cancer Research · doi:10.1158/0008-5472.can-11-1715 · Cited by 129
Takahashi, S., Saegusa, J., Sendo, S., Okano, T., Akashi, K., Irino, Y., & Morinobu, A. (2017) · Arthritis Research & Therapy · doi:10.1186/s13075-017-1283-3 · Cited by 129
Grigorian, A., Araujo, L., Naidu, N. N., Place, D. J., Choudhury, B., & Demetriou, M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.277814 · Cited by 132
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Moloughney, J. G., Kim, P. K., Vega-Cotto, N. M., Wu, C., Zhang, S., Adlam, M., Lynch, T. P., Chou, P.-C., Rabinowitz, J. D., Werlen, G., et al. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.07.015 · Cited by 129
Self-citationGameiro, P. A., Laviolette, L. A., Kelleher, J. K., Iliopoulos, O., & Stephanopoulos, G. N. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.396796 · Cited by 126
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Cohen, R., Neuzillet, C., Tijeras‐Raballand, A., Faivre, S. J., Gramont, A. D. E., & Raymond, É. (2015) · Oncotarget · doi:10.18632/oncotarget.4160 · Cited by 119
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Metadata
- Authors
- Wellen, K. E., Lu, C., Mancuso, A., Lemons, J. M. S., Ryczko, M., Dennis, J. W., Rabinowitz, J. D., Coller, H. A., & Thompson, C. B.
- Affiliations
- University of Pennsylvania (US)
- Princeton University (US)
- Mount Sinai Hospital (CA)
- ORCID
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2010-11-24
- Volume
- 24
- Issue
- 24
- Pages
- 2784-2799
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC3003197
- OpenAlex
- W2034586537
- Cited by
- 377
- References
- 55
- Citations by year
- 2026: 14 · 2025: 15 · 2024: 14 · 2023: 15 · 2022: 29 · 2021: 25 · 2020: 17 · 2019: 24 · 2018: 36 · 2017: 24 · 2016: 28 · 2015: 29 · 2014: 34 · 2013: 26 · 2012: 35
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Damon Runyon Cancer Research Foundation
- National Institutes of Health
- National Cancer Institute (P01CA104838, R01CA105463)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- hexosamine biosynthetic pathway, glutamine uptake, glucose metabolism, interleukin-3, CD123, N-acetylglucosamine, TCA cycle, mitochondrial metabolism, glucose deprivation, cell growth, growth factor signaling, receptor down-regulation
- MeSH terms
- Acetylglucosamine, Animals, Atrophy, Biological Transport, Cell Survival, Citric Acid Cycle, Glucose, Glutamine, Hexosamines, Interleukin-3, Signal Transduction, Intercellular Signaling Peptides and Proteins, Mice, Metabolic Networks and Pathways
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