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Nuclear Translocation of the Epidermal Growth Factor Receptor Family Membrane Tyrosine Kinase Receptors

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Author(s): Wang, SC (Wang, Shao-Chun); Hung, MC (Hung, Mien-Chie)

Title: Nuclear Translocation of the Epidermal Growth Factor Receptor Family Membrane Tyrosine Kinase Receptors

Source: CLINICAL CANCER RESEARCH, 15 (21): 6484-6489 NOV 1 2009 Language: English

Document Type: Article

KeyWords Plus: DEPENDENT PROTEIN-KINASE; SQUAMOUS CARCINOMA-CELLS;

BREAST-CANCER; ERBB RECEPTORS; EGF RECEPTOR; INTRACELLULAR DOMAIN;

PROSTATE-CANCER; GENE-EXPRESSION; SIGNALING NETWORK; INDUCED APOPTOSIS

Abstract: Integral membrane proteins contain a hydrophobic transmembrane domain and mainly locate in the plasma membrane lipid bilayer. The receptor tyrosine kinases (RTK) of the epidermal growth factor receptor (EGFR) superfamily, including ErbB-1, ErbB-2, ErbB-3, and ErbB-4, constitute an important group of such membrane proteins, which have a profound impact on cancer initiation, progression, and patient outcome. Although studies of their functions have conventionally focused on their membrane-associated forms, documented observations of the presence of these membrane receptors and their functioning partners in the nucleus have reshaped the intracellular geography and highlight the need to modify the central dogma. The ErbB proteins in the membrane can translocate to the nucleus through different mechanisms. Nuclear RTKs regulate a variety of cellular functions, such as cell proliferation, DNA damage repair, and signal transduction, both in normal tissues and in human cancer cell. In addition, they play important roles in determining cancer response to cancer therapy. Nuclear presence of these ErbB proteins is emerging as an important marker in human cancers. An integrated picture of the RTK-centered signaling transduction network extending from the membrane-cytoplasm boundary to the nuclear compartment is looming in the foreseeable horizon for clinical application. (Clin Cancer Res 2009;15(21):6484-9)

Addresses: [Wang, Shao-Chun; Hung, Mien-Chie] Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA; [Wang, Shao-Chun] Univ Cincinnati, Coll Med, Dept Canc & Cell Biol, Cincinnati, OH USA; [Hung, Mien-Chie] Asia Univ, Taichung, Taiwan Reprint Address: Hung, MC, Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Unit 108,1515 Holcombe Blvd, Houston, TX 77030 USA.

E-mail Address: mhung@mdanderson.org Funding Acknowledgement:

Funding Agency Grant Number

National Institutes of Health (NIH) R01 CA109311

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Breast Cancer SPORE CA1 16199 University of Texas M. D. Anderson Cancer Center/China Medical

University Hospital Sister Institution Fund

University of Cincinnati College of Medicine

KGO80540 DOD PCRP 0810443

National Institutes of Health (NIH) R01 CA109311, Breast Cancer SPORE CA1 16199, and the University of Texas M. D. Anderson Cancer Center/China Medical University Hospital Sister Institution Fund (to M.-C. Hung). S.-C. Wang is supported by a start-up fund from the University of Cincinnati College of Medicine, the Susan Komen Award KGO80540, and DOD PCRP 0810443.

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Publisher: AMER ASSOC CANCER RESEARCH

Publisher Address: 615 CHESTNUT ST, 17TH FLOOR, PHILADELPHIA, PA 19106-4404 USA

ISSN: 1078-0432

DOI: 10.1158/1078-0432.CCR-08-2813

29-char Source Abbrev.: CLIN CANCER RES ISO Source Abbrev.: Clin. Cancer Res.

Source Item Page Count: 6 Subject Category: Oncology ISI Document Delivery No.: 513CP

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