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PTEN/MMAC1 expression in melanoma resection specimens
PTEN/MMAC1, a tumour suppressor gene located on chromosome 10q23.3, has been found to be deleted in several types of human malignancies. As the chromosomal region 10q22-qter commonly is affected by losses in melanomas, we addressed this gene as tumour suppressor candidate in melanomas. Investigating...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376294/ https://www.ncbi.nlm.nih.gov/pubmed/12454773 http://dx.doi.org/10.1038/sj.bjc.6600653 |
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author | Deichmann, M Thome, M Benner, A Egner, U Hartschuh, W Näher, H |
author_facet | Deichmann, M Thome, M Benner, A Egner, U Hartschuh, W Näher, H |
author_sort | Deichmann, M |
collection | PubMed |
description | PTEN/MMAC1, a tumour suppressor gene located on chromosome 10q23.3, has been found to be deleted in several types of human malignancies. As the chromosomal region 10q22-qter commonly is affected by losses in melanomas, we addressed this gene as tumour suppressor candidate in melanomas. Investigating PTEN/MMAC1 expression at mRNA level by semi-quantitative reverse transcription-polymerase chain reaction, we did not find a statistically significant down-regulation in melanoma resection specimens in comparison to acquired melanocytic nevi from which melanomas quite often are known to arise. Upon immunohistochemistry, PTEN/MMAC1 protein expression in melanomas was not lost. Sequencing the PTEN/MMAC1 cDNAs in 26 melanoma resection specimens (21 primary melanomas, five metastases), we detected three point mutations and two nucleotide deletions which did not represent genetic polymorphisms. With respect to the predicted protein sequences, all three point mutations were silent whereas the two frame shifts at the extreme C-terminus resulted in a loss of the putative PDZ-targeting consensus sequence. As loss of this motif possibly impairs localization and function of PTEN/MMAC1 in the two corresponding primary tumours, alterations of this tumour suppressor protein may participate in some melanomas. British Journal of Cancer (2002) 87, 1431–1436. doi:10.1038/sj.bjc.6600653 www.bjcancer.com © 2002 Cancer Research UK |
format | Text |
id | pubmed-2376294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23762942009-09-10 PTEN/MMAC1 expression in melanoma resection specimens Deichmann, M Thome, M Benner, A Egner, U Hartschuh, W Näher, H Br J Cancer Molecular and Cellular Pathology PTEN/MMAC1, a tumour suppressor gene located on chromosome 10q23.3, has been found to be deleted in several types of human malignancies. As the chromosomal region 10q22-qter commonly is affected by losses in melanomas, we addressed this gene as tumour suppressor candidate in melanomas. Investigating PTEN/MMAC1 expression at mRNA level by semi-quantitative reverse transcription-polymerase chain reaction, we did not find a statistically significant down-regulation in melanoma resection specimens in comparison to acquired melanocytic nevi from which melanomas quite often are known to arise. Upon immunohistochemistry, PTEN/MMAC1 protein expression in melanomas was not lost. Sequencing the PTEN/MMAC1 cDNAs in 26 melanoma resection specimens (21 primary melanomas, five metastases), we detected three point mutations and two nucleotide deletions which did not represent genetic polymorphisms. With respect to the predicted protein sequences, all three point mutations were silent whereas the two frame shifts at the extreme C-terminus resulted in a loss of the putative PDZ-targeting consensus sequence. As loss of this motif possibly impairs localization and function of PTEN/MMAC1 in the two corresponding primary tumours, alterations of this tumour suppressor protein may participate in some melanomas. British Journal of Cancer (2002) 87, 1431–1436. doi:10.1038/sj.bjc.6600653 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-12-02 2002-12-02 /pmc/articles/PMC2376294/ /pubmed/12454773 http://dx.doi.org/10.1038/sj.bjc.6600653 Text en Copyright © 2002 Cancer Research UK 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 | Molecular and Cellular Pathology Deichmann, M Thome, M Benner, A Egner, U Hartschuh, W Näher, H PTEN/MMAC1 expression in melanoma resection specimens |
title | PTEN/MMAC1 expression in melanoma resection specimens |
title_full | PTEN/MMAC1 expression in melanoma resection specimens |
title_fullStr | PTEN/MMAC1 expression in melanoma resection specimens |
title_full_unstemmed | PTEN/MMAC1 expression in melanoma resection specimens |
title_short | PTEN/MMAC1 expression in melanoma resection specimens |
title_sort | pten/mmac1 expression in melanoma resection specimens |
topic | Molecular and Cellular Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376294/ https://www.ncbi.nlm.nih.gov/pubmed/12454773 http://dx.doi.org/10.1038/sj.bjc.6600653 |
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