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The expression and localisation of beta-nerve growth factor (beta-NGF) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation.

beta-NGF is a determinant of sympathetic innervation and a neural differentiation factor. In the present study, we have examined 15 benign prostatic hyperplastic and 15 prostate cancer patients for the expression and localisation of beta-NGF by reverse transcription-polymerase chain reaction (RT-PCR...

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Autores principales: Paul, A. B., Grant, E. S., Habib, F. K.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074798/
https://www.ncbi.nlm.nih.gov/pubmed/8980402
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author Paul, A. B.
Grant, E. S.
Habib, F. K.
author_facet Paul, A. B.
Grant, E. S.
Habib, F. K.
author_sort Paul, A. B.
collection PubMed
description beta-NGF is a determinant of sympathetic innervation and a neural differentiation factor. In the present study, we have examined 15 benign prostatic hyperplastic and 15 prostate cancer patients for the expression and localisation of beta-NGF by reverse transcription-polymerase chain reaction (RT-PCR), Western blotting, immunohistochemistry and ELISA. We have correlated the beta-NGF concentrations to prostate morphometry and neuroendocrine differentiation. The presence of beta NGF mRNA transcripts was confirmed by RT-PCR where a 542 bp product was found with specific primers for the human beta-NGF cDNA sequence. The presence of the peptide was also confirmed by Western blot analysis which showed a protein co-migrating with recombinant human beta-NGF. Our results demonstrate that beta-NGF is localised to prostate epithelium, and the concentrations of the peptide were not significantly different in malignant (mean +/- s.d.; 3100 +/- 1502 pg g-1 wet weight of tissue) than in benign tissues (1992 +/- 684 pg g-1, P = 0.512). We were, however, unable to correlate the concentrations of beta-NGF to neuroendocrine differentiation in malignant tissues. Clearly, the present study demonstrates that beta-NGF is a product of the prostate and may be involved in the control of the sympathetic innervation of the human prostate. IMAGES:
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spelling pubmed-20747982009-09-10 The expression and localisation of beta-nerve growth factor (beta-NGF) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation. Paul, A. B. Grant, E. S. Habib, F. K. Br J Cancer Research Article beta-NGF is a determinant of sympathetic innervation and a neural differentiation factor. In the present study, we have examined 15 benign prostatic hyperplastic and 15 prostate cancer patients for the expression and localisation of beta-NGF by reverse transcription-polymerase chain reaction (RT-PCR), Western blotting, immunohistochemistry and ELISA. We have correlated the beta-NGF concentrations to prostate morphometry and neuroendocrine differentiation. The presence of beta NGF mRNA transcripts was confirmed by RT-PCR where a 542 bp product was found with specific primers for the human beta-NGF cDNA sequence. The presence of the peptide was also confirmed by Western blot analysis which showed a protein co-migrating with recombinant human beta-NGF. Our results demonstrate that beta-NGF is localised to prostate epithelium, and the concentrations of the peptide were not significantly different in malignant (mean +/- s.d.; 3100 +/- 1502 pg g-1 wet weight of tissue) than in benign tissues (1992 +/- 684 pg g-1, P = 0.512). We were, however, unable to correlate the concentrations of beta-NGF to neuroendocrine differentiation in malignant tissues. Clearly, the present study demonstrates that beta-NGF is a product of the prostate and may be involved in the control of the sympathetic innervation of the human prostate. IMAGES: Nature Publishing Group 1996-12 /pmc/articles/PMC2074798/ /pubmed/8980402 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
Paul, A. B.
Grant, E. S.
Habib, F. K.
The expression and localisation of beta-nerve growth factor (beta-NGF) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation.
title The expression and localisation of beta-nerve growth factor (beta-NGF) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation.
title_full The expression and localisation of beta-nerve growth factor (beta-NGF) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation.
title_fullStr The expression and localisation of beta-nerve growth factor (beta-NGF) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation.
title_full_unstemmed The expression and localisation of beta-nerve growth factor (beta-NGF) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation.
title_short The expression and localisation of beta-nerve growth factor (beta-NGF) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation.
title_sort expression and localisation of beta-nerve growth factor (beta-ngf) in benign and malignant human prostate tissue: relationship to neuroendocrine differentiation.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074798/
https://www.ncbi.nlm.nih.gov/pubmed/8980402
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