Literature DB >> 30097778

EGFR Trafficking in Physiology and Cancer.

Giusi Caldieri1,2, Maria Grazia Malabarba1,2, Pier Paolo Di Fiore1,2, Sara Sigismund3,4.   

Abstract

Signaling from the epidermal growth factor receptor (EGFR) elicits multiple biological responses, including cell proliferation, migration, and survival. Receptor endocytosis and trafficking are critical physiological processes that control the strength, duration, diversification, and spatial restriction of EGFR signaling through multiple mechanisms, which we review in this chapter. These mechanisms include: (i) regulation of receptor density and activation at the cell surface; (ii) concentration of receptors into distinct nascent endocytic structures; (iii) commitment of the receptor to different endocytic routes; (iv) endosomal sorting and postendocytic trafficking of the receptor through distinct pathways, and (v) recycling to restricted regions of the cell surface. We also highlight how communication between organelles controls EGFR activity along the endocytic route. Finally, we illustrate how abnormal trafficking of EGFR oncogenic mutants, as well as alterations of the endocytic machinery, contributes to aberrant EGFR signaling in cancer.

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Year:  2018        PMID: 30097778     DOI: 10.1007/978-3-319-96704-2_9

Source DB:  PubMed          Journal:  Prog Mol Subcell Biol        ISSN: 0079-6484


  19 in total

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Review 5.  Epidermal Growth Factor Receptor's Function in Cutaneous Squamous Cell Carcinoma and Its Role as a Therapeutic Target in the Age of Immunotherapies.

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10.  VEGFR-1 Regulates EGF-R to Promote Proliferation in Colon Cancer Cells.

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