Abstract | INTRODUCTION: METHODS AND RESULTS: Disruption of Gnas exon 2 on either the maternal or paternal allele (Gnas(E2-/+)) results in fibromas or angiofibromas on the ears, paws and tail beginning at 4 months of age. The tumors were composed of fibroblastic cell proliferation with collagen and elastin deposition and calcification, and seemed to be associated with mechanical skin damage. The presence of calcification was associated with greater amounts of matrix metalloproteinase-2, suggesting an association between calcium deposition and extracellular matrix degradation. Osteoblast-specific markers were absent, consistent with the calcification not being secondary to ossification. Molecular studies showed that the tumors were not associated with deletion of the wild-type allele, making it unlikely that these tumors resulted from homozygous loss of G(s)alpha. CONCLUSIONS: These findings provide in vivo evidence that G(s)alpha pathways inhibit fibroblast and endothelial proliferation and matrix deposition.
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Authors | Akio Sakamoto, Lee S Weinstein, Antonius Plagge, Michael Eckhaus, Gavin Kelsey |
Journal | Endocrine research
(Endocr Res)
Vol. 34
Issue 1-2
Pg. 1-9
( 2009)
ISSN: 1532-4206 [Electronic] England |
PMID | 19557586
(Publication Type: Journal Article, Research Support, N.I.H., Intramural)
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Chemical References |
- Chromogranins
- Collagen
- Elastin
- Gnas protein, mouse
- GTP-Binding Protein alpha Subunits, Gs
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Topics |
- Angiofibroma
(genetics, pathology, physiopathology)
- Animals
- Calcinosis
(etiology)
- Chromogranins
- Collagen
(metabolism)
- Elastin
(metabolism)
- Fibroma
(genetics, pathology, physiopathology)
- GTP-Binding Protein alpha Subunits, Gs
(genetics, physiology)
- Mice
- Skin Neoplasms
(genetics, pathology, physiopathology)
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