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Article: Gastrin-releasing peptide receptor-mediated autocrine growth in squamous cell carcinoma of the head and neck

TitleGastrin-releasing peptide receptor-mediated autocrine growth in squamous cell carcinoma of the head and neck
Authors
Issue Date2002
Citation
Journal of the National Cancer Institute, 2002, v. 94 n. 5, p. 375-383 How to Cite?
AbstractBackground: Gastrin-releasing peptide receptor (GRPR)-mediated autocrine growth appears to be an early marker of susceptibility to tobacco-related lung cancers. Because expression of GRPR, however, has not been reported in squamous cell carcinoma of the head and neck (SCCHN), we investigated its expression and that of its ligand GRP in normal mucosa and SCCHN tissues and the involvement of these proteins in the proliferation of SCCHN cells. Methods: We assessed GRPR messenger RNA (mRNA) expression in specimens from 25 patients with SCCHN, six control noncancer patients, and 14 SCCHN cell lines by use of quantitative reverse transcriptase-polymerase chain reaction. We used neutralizing GRP monoclonal antibody 2A11 to block the GRP-GRPR interaction in SCCHN cell lines and xenografts and assessed the antibody's effect on proliferation by counting cultured cells or measuring xenograft tumor volume in vivo. All statistical tests were two-sided. Results: Tumor and mucosa tissues, respectively, from SCCHN patients expressed sixfold and fourfold higher levels of GRPR mRNA than normal mucosa tissue from noncancer patients (P<.001). The levels of GRPR expression in the tumor and adjacent normal epithelium of individual patients with SCCHN were correlated (r=.652; P=.001), suggesting that increased GRPR expression is an early event in SCCHN formation. SCCHN cells expressed fivefold higher levels of GRPR mRNA than did cultured normal mucosal epithelial cells (P=.005). GRP stimulated proliferation of SCCHN cells in a dose-dependent fashion (P = .006). Neutralizing GRP monoclonal antibody 2A11 inhibited SCCHN cell proliferation in vitro and in vivo. Median survival was 54 months in patients with higher levels of GRPR mRNA and was not reached in those with lower levels. Conclusions: GRP and GRPR appear to participate in an autocrine regulatory pathway in SCCHN. Thus, strategies that specifically target GRP and/or GRPR may be effective therapeutic approaches for this disease.
Persistent Identifierhttp://hdl.handle.net/10722/194130
ISSN
2015 Impact Factor: 11.37
2015 SCImago Journal Rankings: 6.192
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLango, MN-
dc.contributor.authorDyer, KF-
dc.contributor.authorLui, VWY-
dc.contributor.authorGooding, WE-
dc.contributor.authorGubish, C-
dc.contributor.authorSiegfried, JM-
dc.contributor.authorGrandis, JR-
dc.date.accessioned2014-01-30T03:32:12Z-
dc.date.available2014-01-30T03:32:12Z-
dc.date.issued2002-
dc.identifier.citationJournal of the National Cancer Institute, 2002, v. 94 n. 5, p. 375-383-
dc.identifier.issn0027-8874-
dc.identifier.urihttp://hdl.handle.net/10722/194130-
dc.description.abstractBackground: Gastrin-releasing peptide receptor (GRPR)-mediated autocrine growth appears to be an early marker of susceptibility to tobacco-related lung cancers. Because expression of GRPR, however, has not been reported in squamous cell carcinoma of the head and neck (SCCHN), we investigated its expression and that of its ligand GRP in normal mucosa and SCCHN tissues and the involvement of these proteins in the proliferation of SCCHN cells. Methods: We assessed GRPR messenger RNA (mRNA) expression in specimens from 25 patients with SCCHN, six control noncancer patients, and 14 SCCHN cell lines by use of quantitative reverse transcriptase-polymerase chain reaction. We used neutralizing GRP monoclonal antibody 2A11 to block the GRP-GRPR interaction in SCCHN cell lines and xenografts and assessed the antibody's effect on proliferation by counting cultured cells or measuring xenograft tumor volume in vivo. All statistical tests were two-sided. Results: Tumor and mucosa tissues, respectively, from SCCHN patients expressed sixfold and fourfold higher levels of GRPR mRNA than normal mucosa tissue from noncancer patients (P<.001). The levels of GRPR expression in the tumor and adjacent normal epithelium of individual patients with SCCHN were correlated (r=.652; P=.001), suggesting that increased GRPR expression is an early event in SCCHN formation. SCCHN cells expressed fivefold higher levels of GRPR mRNA than did cultured normal mucosal epithelial cells (P=.005). GRP stimulated proliferation of SCCHN cells in a dose-dependent fashion (P = .006). Neutralizing GRP monoclonal antibody 2A11 inhibited SCCHN cell proliferation in vitro and in vivo. Median survival was 54 months in patients with higher levels of GRPR mRNA and was not reached in those with lower levels. Conclusions: GRP and GRPR appear to participate in an autocrine regulatory pathway in SCCHN. Thus, strategies that specifically target GRP and/or GRPR may be effective therapeutic approaches for this disease.-
dc.languageeng-
dc.relation.ispartofJournal of the National Cancer Institute-
dc.titleGastrin-releasing peptide receptor-mediated autocrine growth in squamous cell carcinoma of the head and neck-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.pmid11880476-
dc.identifier.scopuseid_2-s2.0-0037029025-
dc.identifier.volume94-
dc.identifier.issue5-
dc.identifier.spage375-
dc.identifier.epage383-
dc.identifier.isiWOS:000174198700011-

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