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PKM2 Phosphorylates Histone H3 and Promotes Gene Transcription and Tumorigenesis
Open accessAbstract
Tumor-specific pyruvate kinase M2 (PKM2) is essential for the Warburg effect. In addition to its well-established role in aerobic glycolysis, PKM2 directly regulates gene transcription. However, the mechanism underlying this nonmetabolic function of PKM2 remains elusive. We show here that PKM2 directly binds to histone H3 and phosphorylates histone H3 at T11 upon EGF receptor activation. This phosphorylation is required for the dissociation of HDAC3 from the CCND1 and MYC promoter regions and subsequent acetylation of histone H3 at K9. PKM2-dependent histone H3 modifications are instrumental in EGF-induced expression of cyclin D1 and c-Myc, tumor cell proliferation, cell-cycle progression, and brain tumorigenesis. In addition, levels of histone H3 T11 phosphorylation correlate with nuclear PKM2 expression levels, glioma malignancy grades, and prognosis. These findings highlight the role of PKM2 as a protein kinase in its nonmetabolic functions of histone modification, which is essential for its epigenetic regulation of gene expression and tumorigenesis.
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“PKM2 may also exert some of its effects on cell proliferation through nonmetabolic functions, including transcriptional and epigenetic regulation (61, 62).”
From Fueling Immunity: Insights into Metabolism and Lymphocyte Function (2013) · cites this paper as [62]
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Cites
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197
Regulation of cancer cell metabolism
Cairns, R. A., Harris, I. S., & Mak, T. W. (2011) · Nature Reviews Cancer · doi:10.1038/nrc2981 · Cited by 4,744
Otto Warburg's contributions to current concepts of cancer metabolism
Koppenol, W. H., Bounds, P. L., & Dang, C. V. (2011) · Nature Reviews Cancer · doi:10.1038/nrc3038 · Cited by 3,427
The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth
Christofk, H. R., Vander Heiden, M. G., Harris, M. H., Ramanathan, A., Gerszten, R. E., Wei, R., Fleming, M. D., Schreiber, S. L., & Cantley, L. C. (2008) · Nature · doi:10.1038/nature06734 · Cited by 2,820
Cancer cell metabolism: warburg and beyond
Hsu, P. P., & Sabatini, D. M. (2008) · Cell · doi:10.1016/j.cell.2008.08.021 · Cited by 2,452 · cited 4×
“…to function like fetal cells and to use a large fraction of glucose metabolites to synthesize macromolecules (such as amino acids, phospholipids, and nucleic acids), which support tumor cell growth (Cairns et al., 2011; Hsu and Sabatini, 2008; Koppenol et al., 2011; Vander Heiden et al., 2009).”
InfluentialMalignant astrocytic glioma: genetics, biology, and paths to treatment
Furnari, F. B., Fenton, T., Bachoo, R. M., Mukasa, A., Stommel, J. M., Stegh, A., Hahn, W. C., Ligon, K. L., Louis, D. N., Brennan, C., et al. (2007) · Genes & Development · doi:10.1101/gad.1596707 · Cited by 2,316
Nicholson, R., Gee, J., & Harper, M. (2001) · European Journal of Cancer · doi:10.1016/s0959-8049(01)00231-3 · Cited by 2,132
Pyruvate Kinase M2 Is a PHD3-Stimulated Coactivator for Hypoxia-Inducible Factor 1
Luo, W., Hu, H., Chang, R., Zhong, J., Knabel, M., O'Meally, R., Cole, R. N., Pandey, A., & Semenza, G. L. (2011) · Cell · doi:10.1016/j.cell.2011.03.054 · Cited by 1,463
Nuclear PKM2 regulates β-catenin transactivation upon EGFR activation
Yang, W., Xia, Y., Ji, H., Zheng, Y., Liang, J., Huang, W., Gao, X., Aldape, K., & Lu, Z. (2011) · Nature · doi:10.1038/nature10598 · Cited by 1,051
Self-citationPyruvate kinase M2 is a phosphotyrosine-binding protein
Christofk, H. R., Vander Heiden, M. G., Wu, N., Asara, J. M., & Cantley, L. C. (2008) · Nature · doi:10.1038/nature06667 · Cited by 995
Majumder, P. K., Febbo, P. G., Bikoff, R., Berger, R., Xue, Q., McMahon, L. M., Manola, J., Brugarolas, J., McDonnell, T. J., Golub, T. R., et al. (2004) · Nature Medicine · doi:10.1038/nm1052 · Cited by 964
Phosphorylation of β-Catenin by AKT Promotes β-Catenin Transcriptional Activity
Fang, D., Hawke, D. H., Zheng, Y., Xia, Y., Meisenhelder, J., Nika, H., Mills, G. B., Kobayashi, R., Hunter, T. R., & Lu, Z. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611871200 · Cited by 888
Self-citationUniversal and Confident Phosphorylation Site Localization Using phosphoRS
Taus, T., Köcher, T., Pichler, P., Paschke, C., Schmidt, A., Henrich, C., & Mechtler, K. (2011) · Journal of Proteome Research · doi:10.1021/pr200611n · Cited by 855
Pyruvate kinase type M2 and its role in tumor growth and spreading
Mazurek, S., Boschek, C. B., Hugo, F., & Eigenbrodt, E. (2005) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2005.04.009 · Cited by 812
Pyruvate Kinase M2 Regulates Gene Transcription by Acting as a Protein Kinase
Gao, X., Wang, H., Yang, J. J., Liu, X., & Liu, Z.-R. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.01.001 · Cited by 772
Lu, Z., Ghosh, S., Wang, Z.-Y., & Hunter, T. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00304-0 · Cited by 682
Self-citationGenes of glycolysis are ubiquitously overexpressed in 24 cancer classes
Altenberg, B., & Greulich, K. O. (2004) · Genomics · doi:10.1016/j.ygeno.2004.08.010 · Cited by 662
Evidence for an Alternative Glycolytic Pathway in Rapidly Proliferating Cells
Heiden, M. G. V., Locasale, J. W., Swanson, K. D., Sharfi, H., Heffron, G. J., Amador‐Noguez, D., Christofk, H. R., Wagner, G., Rabinowitz, J. D., Asara, J. M., et al. (2010) · Science · doi:10.1126/science.1188015 · Cited by 648
Frequent expression of a mutant epidermal growth factor receptor in multiple human tumors.
Moscatello, D. K., Holgado-Madruga, M., Godwin, A. K., Ramirez, G., Gunn, G. R., Zoltick, P. W., Biegel, J. A., Hayes, R. L., & Wong, A. J. (1995) · PubMed · Cited by 637
The Language of Histone Crosstalk
Lee, J., Smith, E. R., & Shilatifard, A. (2010) · Cell · doi:10.1016/j.cell.2010.08.011 · Cited by 598
Noguchi, T., Inoue, H., & Tanaka, T. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)67091-7 · Cited by 544
Different Roles for Cyclins D1 and E in Regulation of the G1-to-S Transition
Resnitzky, D., & Reed, S. I. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.7.3463 · Cited by 472
Structural Basis for Tumor Pyruvate Kinase M2 Allosteric Regulation and Catalysis ,
Dombrauckas, J. D., Santarsiero, B. D., & Mesecar, A. D. (2005) · Biochemistry · doi:10.1021/bi0474923 · Cited by 414
Mechanism for the stimulation of gluconeogenesis by fatty acids in perfused rat liver.
WILLIAMSON, J. R., Kreisberg, R. A., & Felts, P. W. (1966) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.56.1.247 · Cited by 387
Crosstalk among Histone Modifications
Suganuma, T., & Workman, J. L. (2008) · Cell · doi:10.1016/j.cell.2008.10.036 · Cited by 385
Activation of Protein Kinase C Triggers Its Ubiquitination and Degradation
Lu, Z., Liu, D., Hornia, A., Devonish, W., Pagano, M., & Foster, D. A. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.2.839 · Cited by 334
Self-citationJi, H., Wang, J., Nika, H., Hawke, D., Keezer, S., Ge, Q., Fang, B., Fang, X., Fang, D., Litchfield, D. W., et al. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.09.034 · Cited by 270
Self-citationShimada, M., Niida, H., Zineldeen, D. H., Tagami, H., Tanaka, M., Saito, H., & Nakanishi, M. (2008) · Cell · doi:10.1016/j.cell.2007.12.013 · Cited by 263
Metzger, E., Yin, N., Wissmann, M., Kunowska, N., Fischer, K. J., Friedrichs, N., Patnaik, D., Higgins, J. M. G., Potier, N., Scheidtmann, K., et al. (2007) · Nature Cell Biology · doi:10.1038/ncb1668 · Cited by 233
Lee, J., Kim, H., Han, Y., & Kim, J. (2007) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2007.11.009 · Cited by 215
Novel mitosis-specific phosphorylation of histone H3 at Thr11 mediated by Dlk/ZIP kinase
Preuß, U. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg176 · Cited by 191
Nuclear Translocation of the Tumor Marker Pyruvate Kinase M2 Induces Programmed Cell Death
Steták, A., Veress, R., Ovádi, J., Csermely, P., Kéri, G., & Ullrich, A. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-2870 · Cited by 183
Therapeutic targeting of epidermal growth factor receptor in human cancer: successes and limitations
Wykosky, J., Fenton, T. R., Furnari, F. B., & Cavenee, W. K. (2011) · 癌症:英文版 · doi:10.5732/cjc.010.10542 · Cited by 158
When Signaling Kinases Meet Histones and Histone Modifiers in the Nucleus
Baek, S. H. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.03.022 · Cited by 149
Pérez-Cadahı́a, B., Drobic, B., & Davie, J. (2009) · Biochemistry and Cell Biology · doi:10.1139/o09-053 · Cited by 141
Regulation of Cell Proliferation by Interleukin-3-induced Nuclear Translocation of Pyruvate Kinase
Hoshino, A., Hirst, J. A., & Fujii, H. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700094200 · Cited by 96
Mazurek, S. (2008) · Ernst Schering Research Foundation workshop/Ernst Schering Foundation Symposium proceedings · doi:10.1007/2789_2008_091 · Cited by 76
Xia, Y., Wang, J., Liu, T.-J., Yung, W. K. A., Hunter, T. R., & Lu, Z. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.01.005 · Cited by 76
Self-citationWnt-independent beta-catenin transactivation in tumor development.
Lu, Z., & Hunter, T. R. (2004) · PubMed · Cited by 55
Self-citationLu, Z. (2011) · 癌症:英文版 · doi:10.5732/cjc.011.10446 · Cited by 54
Self-citationGomez‐Manzano, C., Alonso, M. M., Yung, W. K. A., McCormick, F. P., Curiel, D. T., Lang, F. F., Jiang, H., Bekele, B. N., Zhou, X. C., Alemany, R., et al. (2006) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-05-1892 · Cited by 51
Wnt-Independent ?-catenin Transactivation in Tumor Developement
Lu, Z., & Hunter, T. (2004) · Cell Cycle · doi:10.4161/cc.3.5.885 · Cited by 32
Self-citationMellati, A. A., Yücel, M., Altınörs, N., & Gündüz, U. (1992) · PubMed · Cited by 23
Zhimin, & LU, L. (2012) · 癌症:英文版 · Cited by 21
Checkpoints meet the transcription at a novel histone milestone (H3-T11)
Shimada, M., & Nakanishi, M. (2008) · Cell Cycle · doi:10.4161/cc.7.11.6062 · Cited by 13
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Fueling Immunity: Insights into Metabolism and Lymphocyte Function
Pearce, E. L., Poffenberger, M. C., Chang, C.-H., & Jones, R. G. (2013) · Science · doi:10.1126/science.1242454 · Cited by 1,363
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ERK1/2-dependent phosphorylation and nuclear translocation of PKM2 promotes the Warburg effect
Yang, W., Zheng, Y., Xia, Y., Ji, H., Chen, X., Guo, F., Lyssiotis, C. A., Aldape, K., Cantley, L. C., & Lu, Z. (2012) · Nature Cell Biology · doi:10.1038/ncb2629 · Cited by 926
Self-citation
Metadata
- Authors
- Yang, W., Xia, Y., Hawke, D., Li, X., Liang, J., Xing, D., Aldape, K., Hunter, T., Alfred Yung, W. K., & Lu, Z.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- Tsinghua University (CN)
- Salk Institute for Biological Studies (US)
- Corresponding author
- Lu, Zhimin
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2012-08
- Volume
- 150
- Issue
- 4
- Pages
- 685-696
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC3431020
- OpenAlex
- W2134847995
- Cited by
- 846
- References
- 48
- Citations by year
- 2026: 46 · 2025: 66 · 2024: 63 · 2023: 85 · 2022: 45 · 2021: 75 · 2020: 62 · 2019: 68 · 2018: 58 · 2017: 54 · 2016: 64 · 2015: 51 · 2014: 52 · 2013: 43 · 2012: 9
- FWCI
- 16.46
- Type
- journal article
- Language
- en
- Update notices
- erratum (2014-08-28)
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (CA-16672, R01CA109035, R01CA082683, P30CA016672, P50CA127001)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- PKM2, HDAC3, EGF receptor, cyclin D1, c-Myc, gene transcription, epigenetic regulation, Warburg effect, aerobic glycolysis, brain tumorigenesis, glioma, tumor cell proliferation, cell cycle progression
- MeSH terms
- Thyroid Hormone-Binding Proteins, Animals, Astrocytoma, Carrier Proteins, Cell Line, Cell Transformation, Neoplastic, Epidermal Growth Factor, Female, Glioblastoma, Histones, Humans, Membrane Proteins, Mice, Nude, Neoplasm Transplantation, Thyroid Hormones, Transcription, Genetic, Transplantation, Heterologous, Gene Expression Regulation, Neoplastic, Proto-Oncogene Proteins c-myc, Cyclin D1, Epigenesis, Genetic, Cell Line, Tumor, Mice
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