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DC electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids.
The effects of electrical direct current (DC) field pulses on c-fos expression, growth kinetics and vitality patterns of multicellular tumour spheroids (MCSs) were studied. Monitoring the membrane potential of MCSs by di-8-ANNEPS staining and confocal microscopy during DC electrical field treatment...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2223507/ https://www.ncbi.nlm.nih.gov/pubmed/9166941 |
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author | Sauer, H. Hescheler, J. Reis, D. Diedershagen, H. Niedermeier, W. Wartenberg, M. |
author_facet | Sauer, H. Hescheler, J. Reis, D. Diedershagen, H. Niedermeier, W. Wartenberg, M. |
author_sort | Sauer, H. |
collection | PubMed |
description | The effects of electrical direct current (DC) field pulses on c-fos expression, growth kinetics and vitality patterns of multicellular tumour spheroids (MCSs) were studied. Monitoring the membrane potential of MCSs by di-8-ANNEPS staining and confocal microscopy during DC electrical field treatment revealed a hyperpolarization at the anode-facing side and a depolarization at the cathode-facing side. When a single 500 V m(-1) electrical field pulse with a duration of 60 s was applied to MCSs (150-350 microm in diameter) an enhancement of the growth kinetics within a period of 6 days post pulse was observed. Whereas the volume doubling time amounted to 4-5 days in control samples, it was reduced to 1-2 days in electropulsed MCSs. At day 6 post pulse the diameter of the necrotic core was significantly smaller than the control. The critical diameter for the first appearance of central necrosis amounted to 350 +/- 50 microm in the control and 450 +/- 50 microm in the electropulsed MCSs. Coincidentally, the proliferating rim was increased to 107 +/- 11 microm in electropulsed MCSs as compared with 60 +/- 6 microm in the control. The growth stimulation may be mediated by the proto-oncogene c-fos as its expression increased by a factor of 2.5 within 2 h post pulse. c-fos expression declined towards control values within 8 h post pulse. IMAGES: |
format | Text |
id | pubmed-2223507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22235072009-09-10 DC electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids. Sauer, H. Hescheler, J. Reis, D. Diedershagen, H. Niedermeier, W. Wartenberg, M. Br J Cancer Research Article The effects of electrical direct current (DC) field pulses on c-fos expression, growth kinetics and vitality patterns of multicellular tumour spheroids (MCSs) were studied. Monitoring the membrane potential of MCSs by di-8-ANNEPS staining and confocal microscopy during DC electrical field treatment revealed a hyperpolarization at the anode-facing side and a depolarization at the cathode-facing side. When a single 500 V m(-1) electrical field pulse with a duration of 60 s was applied to MCSs (150-350 microm in diameter) an enhancement of the growth kinetics within a period of 6 days post pulse was observed. Whereas the volume doubling time amounted to 4-5 days in control samples, it was reduced to 1-2 days in electropulsed MCSs. At day 6 post pulse the diameter of the necrotic core was significantly smaller than the control. The critical diameter for the first appearance of central necrosis amounted to 350 +/- 50 microm in the control and 450 +/- 50 microm in the electropulsed MCSs. Coincidentally, the proliferating rim was increased to 107 +/- 11 microm in electropulsed MCSs as compared with 60 +/- 6 microm in the control. The growth stimulation may be mediated by the proto-oncogene c-fos as its expression increased by a factor of 2.5 within 2 h post pulse. c-fos expression declined towards control values within 8 h post pulse. IMAGES: Nature Publishing Group 1997 /pmc/articles/PMC2223507/ /pubmed/9166941 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 Sauer, H. Hescheler, J. Reis, D. Diedershagen, H. Niedermeier, W. Wartenberg, M. DC electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids. |
title | DC electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids. |
title_full | DC electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids. |
title_fullStr | DC electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids. |
title_full_unstemmed | DC electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids. |
title_short | DC electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids. |
title_sort | dc electrical field-induced c-fos expression and growth stimulation in multicellular prostate cancer spheroids. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2223507/ https://www.ncbi.nlm.nih.gov/pubmed/9166941 |
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