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Absence of telomerase activity and telomerase catalytic subunit mRNA in melanocyte cultures
The classic model of activation of telomerase, for which activity has been found in most cancers including cutaneous malignant melanoma (CMM), dictates that enzyme activity is generated by pathological reactivation of telomerase in telomerase-negative somatic cells. However, recent data demonstrated...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374429/ https://www.ncbi.nlm.nih.gov/pubmed/10737388 http://dx.doi.org/10.1054/bjoc.1999.1041 |
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author | Dhaene, K Vancoillie, G Lambert, J Naeyaert, J M Marck, E Van |
author_facet | Dhaene, K Vancoillie, G Lambert, J Naeyaert, J M Marck, E Van |
author_sort | Dhaene, K |
collection | PubMed |
description | The classic model of activation of telomerase, for which activity has been found in most cancers including cutaneous malignant melanoma (CMM), dictates that enzyme activity is generated by pathological reactivation of telomerase in telomerase-negative somatic cells. However, recent data demonstrated physiological up-regulation in some normal cell types when established as proliferating cultures, indicating that, in some cancer types, telomerase is expressed by the process of up-regulation in telomerase-competent precursor cells. In this study, cultures of epidermal melanocytes, progenitor cells of CMM, were established and harvested in the logarithmic phase of growth. Telomerase activity was looked for using a non-isotopic variant of the telomeric repeat amplification protocol, and transcript expression of the hTERT gene, the rate-limiting catalytic telomerase subunit, was investigated by the reverse transcription polymerase chain reaction. Neither telomerase activity nor hTERT mRNA could be detected in proliferating melanocyte cultures. Our in vitro data argue against the model of telomerase as a common biomarker of cell proliferation. The results further suggest that telomerase is tightly controlled in normal melanocytes, and that telomerase is reactivated rather than up-regulated in melanocytic precursors during melanoma initiation or progression. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2374429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23744292009-09-10 Absence of telomerase activity and telomerase catalytic subunit mRNA in melanocyte cultures Dhaene, K Vancoillie, G Lambert, J Naeyaert, J M Marck, E Van Br J Cancer Regular Article The classic model of activation of telomerase, for which activity has been found in most cancers including cutaneous malignant melanoma (CMM), dictates that enzyme activity is generated by pathological reactivation of telomerase in telomerase-negative somatic cells. However, recent data demonstrated physiological up-regulation in some normal cell types when established as proliferating cultures, indicating that, in some cancer types, telomerase is expressed by the process of up-regulation in telomerase-competent precursor cells. In this study, cultures of epidermal melanocytes, progenitor cells of CMM, were established and harvested in the logarithmic phase of growth. Telomerase activity was looked for using a non-isotopic variant of the telomeric repeat amplification protocol, and transcript expression of the hTERT gene, the rate-limiting catalytic telomerase subunit, was investigated by the reverse transcription polymerase chain reaction. Neither telomerase activity nor hTERT mRNA could be detected in proliferating melanocyte cultures. Our in vitro data argue against the model of telomerase as a common biomarker of cell proliferation. The results further suggest that telomerase is tightly controlled in normal melanocytes, and that telomerase is reactivated rather than up-regulated in melanocytic precursors during melanoma initiation or progression. © 2000 Cancer Research Campaign Nature Publishing Group 2000-03 2000-02-01 /pmc/articles/PMC2374429/ /pubmed/10737388 http://dx.doi.org/10.1054/bjoc.1999.1041 Text en Copyright © 2000 Cancer Research Campaign 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 | Regular Article Dhaene, K Vancoillie, G Lambert, J Naeyaert, J M Marck, E Van Absence of telomerase activity and telomerase catalytic subunit mRNA in melanocyte cultures |
title | Absence of telomerase activity and telomerase catalytic subunit mRNA in melanocyte cultures |
title_full | Absence of telomerase activity and telomerase catalytic subunit mRNA in melanocyte cultures |
title_fullStr | Absence of telomerase activity and telomerase catalytic subunit mRNA in melanocyte cultures |
title_full_unstemmed | Absence of telomerase activity and telomerase catalytic subunit mRNA in melanocyte cultures |
title_short | Absence of telomerase activity and telomerase catalytic subunit mRNA in melanocyte cultures |
title_sort | absence of telomerase activity and telomerase catalytic subunit mrna in melanocyte cultures |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374429/ https://www.ncbi.nlm.nih.gov/pubmed/10737388 http://dx.doi.org/10.1054/bjoc.1999.1041 |
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