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Analysis of somatostatin receptor subtype mRNA expression in human breast cancer.

Somatostatin is a widely distributed inhibitory peptide with growth-inhibitory effects in several human tumours, including breast cancer, raising the possibility that it may have therapeutic potential. The effects of somatostatin are mediated via a family of cell-surface receptors that differ in the...

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Autores principales: Evans, A. A., Crook, T., Laws, S. A., Gough, A. C., Royle, G. T., Primrose, J. N.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group|1 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063409/
https://www.ncbi.nlm.nih.gov/pubmed/9062398
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author Evans, A. A.
Crook, T.
Laws, S. A.
Gough, A. C.
Royle, G. T.
Primrose, J. N.
author_facet Evans, A. A.
Crook, T.
Laws, S. A.
Gough, A. C.
Royle, G. T.
Primrose, J. N.
author_sort Evans, A. A.
collection PubMed
description Somatostatin is a widely distributed inhibitory peptide with growth-inhibitory effects in several human tumours, including breast cancer, raising the possibility that it may have therapeutic potential. The effects of somatostatin are mediated via a family of cell-surface receptors that differ in their tissue distribution, pharmacological properties and intracellular response mediators, suggesting that they mediate different functions of the peptide. We have analysed the expression of somatostatin receptor subtype (SSTR1-5) mRNA in normal and malignant breast tissue. Receptor expression was analysed by reverse transcription-polymerase chain reaction (RT-PCR) using receptor subtype-specific primers and by in situ hybridization (ISH) with riboprobes synthesized by in vitro transcription of cloned PCR products. A total of 51 breast carcinomas, 36 samples of matched normal tissue, two axillary node metastases and eight normal/benign breast tissue samples were analysed. SSTR2 expression was ubiquitous in both normal and malignant breast tissue. Expression of SSTR5 was detected in approximately one-third of tumour and normal tissue, but fewer than 13% of all tissues expressed SSTR1, 3 and 4. These data suggest that SSTR2 gene expression is ubiquitous in breast cancer. Although this is unlikely to have diagnostic or prognostic significance, SSTR2-specific somatostatin analogues may have therapeutic potential in breast cancer. IMAGES:
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spelling pubmed-20634092009-09-10 Analysis of somatostatin receptor subtype mRNA expression in human breast cancer. Evans, A. A. Crook, T. Laws, S. A. Gough, A. C. Royle, G. T. Primrose, J. N. Br J Cancer Research Article Somatostatin is a widely distributed inhibitory peptide with growth-inhibitory effects in several human tumours, including breast cancer, raising the possibility that it may have therapeutic potential. The effects of somatostatin are mediated via a family of cell-surface receptors that differ in their tissue distribution, pharmacological properties and intracellular response mediators, suggesting that they mediate different functions of the peptide. We have analysed the expression of somatostatin receptor subtype (SSTR1-5) mRNA in normal and malignant breast tissue. Receptor expression was analysed by reverse transcription-polymerase chain reaction (RT-PCR) using receptor subtype-specific primers and by in situ hybridization (ISH) with riboprobes synthesized by in vitro transcription of cloned PCR products. A total of 51 breast carcinomas, 36 samples of matched normal tissue, two axillary node metastases and eight normal/benign breast tissue samples were analysed. SSTR2 expression was ubiquitous in both normal and malignant breast tissue. Expression of SSTR5 was detected in approximately one-third of tumour and normal tissue, but fewer than 13% of all tissues expressed SSTR1, 3 and 4. These data suggest that SSTR2 gene expression is ubiquitous in breast cancer. Although this is unlikely to have diagnostic or prognostic significance, SSTR2-specific somatostatin analogues may have therapeutic potential in breast cancer. IMAGES: Nature Publishing Group|1 1997 /pmc/articles/PMC2063409/ /pubmed/9062398 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Evans, A. A.
Crook, T.
Laws, S. A.
Gough, A. C.
Royle, G. T.
Primrose, J. N.
Analysis of somatostatin receptor subtype mRNA expression in human breast cancer.
title Analysis of somatostatin receptor subtype mRNA expression in human breast cancer.
title_full Analysis of somatostatin receptor subtype mRNA expression in human breast cancer.
title_fullStr Analysis of somatostatin receptor subtype mRNA expression in human breast cancer.
title_full_unstemmed Analysis of somatostatin receptor subtype mRNA expression in human breast cancer.
title_short Analysis of somatostatin receptor subtype mRNA expression in human breast cancer.
title_sort analysis of somatostatin receptor subtype mrna expression in human breast cancer.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063409/
https://www.ncbi.nlm.nih.gov/pubmed/9062398
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