| Literature DB >> 16463386 |
Alex Starr1, Joel Greif, Akiva Vexler, Maia Ashkenazy-Voghera, Valery Gladesh, Chanan Rubin, Gabriele Kerber, Sylvia Marmor, Shahar Lev-Ari, Moshe Inbar, Yosef Yarden, Rami Ben-Yosef.
Abstract
Clinical and experimental data suggest that ErbB-4, a member of the epidermal growth factor receptor family, may have a role in cancer progression and response to treatment. We found recently, using a retrospective clinical analysis, that expression of ErbB-4 receptor is correlated with metastatic potential and patient survival in non-small-cell lung cancer (NSCLC). The purpose of this work was to correlate the expression of the ErbB-4 and lung cancer cells growth in vitro and in vivo and to determine the therapeutic potential of a monoclonal antibody to ErbB-4 against lung cancer. For this aim, we ectopically expressed ErbB-4 in a human NSCLC cell line that did not express the ErbB-4 protein. Overexpression of ErbB-4 produced a constitutively activated ErbB-4 receptor. The transfected ErbB-4 positive clones showed an increased cell proliferation in vitro and in vivo in comparison with parental ErbB-4 negative cells and with the cells transfected by neomycin-resistant gene. A monoclonal antibody to ErbB-4 showed both an inhibitory effect on growth rate and an increasing apoptotic rate in the cells expressing ErbB-4. The results of the current study provide evidence that ErbB-4 plays a significant role in human lung cancer and may serve as a molecular target for anticancer therapy. 2006 Wiley-Liss, Inc.Entities:
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Year: 2006 PMID: 16463386 DOI: 10.1002/ijc.21818
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396