The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Epidermal Growth Factor Receptor Translocation to the Mitochondria
Open accessAbstract
Co-overexpression of the epidermal growth factor (EGF) receptor (EGFR) and c-Src frequently occurs in human tumors and is linked to enhanced tumor growth. In experimental systems this synergistic growth requires EGF-dependent association of c-Src with the EGFR and phosphorylation of Tyr-845 of the receptor by c-Src. A search for signaling mediators of Tyr(P)-845 revealed that mitochondrial cytochrome c oxidase subunit II (CoxII) binds EGFR in a Tyr(P)-845- and EGF-dependent manner. In cells this association involves translocation of EGFR to the mitochondria, but regulation of this process is ill-defined. The current study demonstrates that c-Src translocates to the mitochondria with similar kinetics as EGFR and that the catalytic activity of EGFR and c-Src as well as endocytosis and a mitochondrial localization signal are required for these events. CoxII can be phosphorylated by EGFR and c-Src, and EGF stimulation reduces Cox activity and cellular ATP, an event that is dependent in large part on EGFR localized to the mitochondria. These findings suggest EGFR plays a novel role in modulating mitochondrial function via its association with, and modification of CoxII.
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Cites
Hypoxia, HIF1 and glucose metabolism in the solid tumour
Denko, N. C. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2468 · Cited by 1,707
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Cited by
EGF receptor trafficking: consequences for signaling and cancer
Tomas, A., Futter, C. E., & Eden, E. R. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2013.11.002 · Cited by 779
Shay, J., Elbaz, H. A., Lee, I., Zielske, S. P., Malek, M. H., & Hüttemann, M. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/181260 · Cited by 279
Self-citationUnderlying features of epigenetic aging clocks in vivo and in vitro.
Liu, Z., Leung, D., Thrush, K., Zhao, W., Ratliff, S., Tanaka, T., Schmitz, L. L., Smith, J. A., Ferrucci, L., & Levine, M. E. (2020) · Aging Cell · doi:10.1111/acel.13229 · Cited by 227
Bhushan, B., & Michalopoulos, G. K. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.109090 · Cited by 66
Hartmann, C., Schwietzer, Y. A., Kummer, D., Kirschnick, N., Hoppe, E., Thüring, E.-M., Glaesner-Ebnet, M., Brinkmann, F., Gerke, V., Reuter, S., et al. (2020) · BMC Molecular and Cell Biology · doi:10.1186/s12860-020-00274-1 · Cited by 32
Metadata
- Authors
- Demory, M. L., Boerner, J. L., Davidson, R., Faust, W., Miyake, T., Lee, I., Hüttemann, M., Douglas, R., Haddad, G., & Parsons, S. J.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2009-12
- Volume
- 284
- Issue
- 52
- Pages
- 36592-36604
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2084688946
- Cited by
- 184
- References
- 2
- FWCI
- 4.62
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Demory, M. L., Boerner, J. L., Davidson, R., Faust, W., Miyake, T., Lee, I., Hüttemann, M., Douglas, R., Haddad, G., & Parsons, S. J. (2009). Epidermal Growth Factor Receptor Translocation to the Mitochondria. Journal of Biological Chemistry. https://doi.org/10.1074/jbc.m109.000760
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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