Expression and Molecular Characterization of the Growth Hormone Receptor in Canine Mammary Tissue and Mammary Tumors
GH synthesis has been documented in canine mammary tissue and mammary tumors. In the present report, the characteristics of the GH receptor (GHR) are studied in these tissues. First, using immunohistochemistry, GHR was found to be present throughout normal and tumorous mammary tissues, being localiz...
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Veröffentlicht in: | Endocrinology (Philadelphia) 1999-12, Vol.140 (12), p.5907-5914 |
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Zusammenfassung: | GH synthesis has been documented in canine mammary tissue and mammary
tumors. In the present report, the characteristics of the GH receptor
(GHR) are studied in these tissues. First, using immunohistochemistry,
GHR was found to be present throughout normal and tumorous mammary
tissues, being localized in epithelial and myoepithelial/spindle cell
components and in the activated fibroblasts of desmoplastic tumor
stroma. GHR expression seemed to be down-regulated only in terminally
differentiated alveoli in normal tissue. GHR immunoreactivity in
particular mammary (adeno)carcinomas was heterogenous.
Second, the canine GHR was characterized at the molecular level.
Northern blot analysis revealed a major GHR transcript of approximately
4.2 kb. The coding sequence of the canine GHR shows extensive homology
with the GHR of several species. Seminested RT-PCR (using primers
annealing in exons 4–5, exon 6, and exon 9) generated, next to the
primary product, four different products in mammary tissues and the
canine mammary tumor cell line CMT-U335, which seemed to be alternative
GHR transcripts. These alternative GHR transcripts were characterized
by exon 8 skipping, exon 7 skipping, and use of alternative splice
donor and acceptor sites. Especially, the transcript that is missing
exon 8 may encode a GH binding protein. In most malignant
mammary samples, only the primary transcript was present; and
alternative transcripts could not be detected. The absence of
alternative GHR transcripts in mammary carcinomas, and thus putative
inhibitors of GH-induced signal transduction, may contribute to
enhanced sensitivity of malignant tumors to GH. |
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ISSN: | 0013-7227 1945-7170 |
DOI: | 10.1210/endo.140.12.7189 |