Critical function for ADAM9 in mouse prostate cancer Journal Article


Authors: Peduto, L.; Reuter, V. E.; Shaffer, D. R.; Scher, H. I.; Blobel, C. P.
Article Title: Critical function for ADAM9 in mouse prostate cancer
Abstract: ADAM9 is a membrane-anchored metalloprotease that is markedly up-regulated in several human carcinomas. Here, we show that ADAM9 is similarly up-regulated in mouse models for prostate, breast, and intestinal carcinoma. To assess whether ADAM9 is critical for the pathogenesis of prostate carcinoma, one of the most common cancers in men, we evaluated how loss of ADAM9 affects tumorigenesis in W10 mice, a mouse model for this disease. In the absence of ADAM9, most tumors in 50-week-old W10 mice were well differentiated, whereas littermate controls expressing wild-type ADAM9 had predominantly poorly differentiated, and in some cases significantly larger, tumors. Moreover, gain-of-function experiments in which ADAM9 was overexpressed in mouse prostate epithelium resulted in significant abnormalities, including epithelial hyperplasia at 4 to 6 months of age, and prostatic intraepithelial neoplasia after 1 year. A potential underlying mechanism for the role of ADAM9 in prostate cancer emerged from cell-based assays: ADAM9 can cleave and release epidermal growth factor and FGFR2iiib from cells, both of which have pivotal functions in the pathogenesis of this disease. Taken together, these results suggest that ADAM9 contributes to the pathogenesis of prostate cancer and potentially also other carcinomas, raising the possibility that ADAM9 might be a good target for antitumor drugs. ©2005 American Association for Cancer Research.
Keywords: epidermal growth factor; controlled study; aged; unclassified drug; nonhuman; animal cell; mouse; animals; mice; animal tissue; animal experiment; animal model; membrane proteins; cell differentiation; mice, inbred c57bl; carcinogenesis; transgenic mouse; mice, transgenic; prostate cancer; prostatic neoplasms; in situ hybridization; rna, messenger; newborn; prostate epithelium; prostatic intraepithelial neoplasia; up-regulation; intestinal neoplasms; fibroblast growth factor 7; fibroblast growth factor receptor 2; receptor, fibroblast growth factor, type 2; metalloproteinase; adam proteins; epithelium hyperplasia; mammary neoplasms, experimental; protein adam9; fibroblast growth factor receptor 2iiib
Journal Title: Cancer Research
Volume: 65
Issue: 20
ISSN: 0008-5472
Publisher: American Association for Cancer Research  
Date Published: 2005-10-15
Start Page: 9312
End Page: 9319
Language: English
DOI: 10.1158/0008-5472.can-05-1063
PUBMED: 16230393
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 53" - "Export Date: 24 October 2012" - "CODEN: CNREA" - "Source: Scopus"
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  1. Lucie Peduto
    2 Peduto
  2. Victor Reuter
    1223 Reuter
  3. Howard Scher
    1129 Scher
  4. David R Shaffer
    25 Shaffer