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Human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation.

A panel of human colonic adenocarcinoma cell lines was examined both for expression of mRNAs of the nitric oxide synthase (NOS) gene family and for evidence of enzymic activity based on citrulline and nitrite (NO2-) formation. Reverse transcription-polymerase chain reaction (RT-PCR), revealed that a...

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Autores principales: Jenkins, D. C., Charles, I. G., Baylis, S. A., Lelchuk, R., Radomski, M. W., Moncada, S.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033551/
https://www.ncbi.nlm.nih.gov/pubmed/7524602
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author Jenkins, D. C.
Charles, I. G.
Baylis, S. A.
Lelchuk, R.
Radomski, M. W.
Moncada, S.
author_facet Jenkins, D. C.
Charles, I. G.
Baylis, S. A.
Lelchuk, R.
Radomski, M. W.
Moncada, S.
author_sort Jenkins, D. C.
collection PubMed
description A panel of human colonic adenocarcinoma cell lines was examined both for expression of mRNAs of the nitric oxide synthase (NOS) gene family and for evidence of enzymic activity based on citrulline and nitrite (NO2-) formation. Reverse transcription-polymerase chain reaction (RT-PCR), revealed that all lines (SW480, SW620, DLD-1 and WiDr) expressed mRNA for the Ca(2+)-dependent endothelial (e)NOS, while SW480 cells also expressed the Ca(2+)-dependent neuronal (n)NOS. The mRNA for the Ca(2+)-independent inducible (i)NOS was expressed both by cytokine-stimulated and by unstimulated SW480, SW620 and DLD-1 cells, but none was seen at any time in the WiDr cells. There was, however, little correlation between mRNA expression and enzymic activity based on citrulline and NO2- formation. Thus none of the cell lines exhibited measurable Ca(2+)-dependent NOS activity, while Ca(2+)-independent NOS activity was seen in all but the WiDr cells. Furthermore, DLD-1 cells generated citrulline with resultant NO2- formation only after stimulation with lipopolysaccharide (LPS) and/or cytokines, while SW480 and SW620 did so constitutively. Thus RT-PCR studies indicate that tumour cells of similar epithelial origin display a diverse pattern of NOS gene family expression, and parallel biochemical studies clearly indicate that such expression does not always result in measurable enzymic activity leading to the generation of NO. IMAGES:
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spelling pubmed-20335512009-09-10 Human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation. Jenkins, D. C. Charles, I. G. Baylis, S. A. Lelchuk, R. Radomski, M. W. Moncada, S. Br J Cancer Research Article A panel of human colonic adenocarcinoma cell lines was examined both for expression of mRNAs of the nitric oxide synthase (NOS) gene family and for evidence of enzymic activity based on citrulline and nitrite (NO2-) formation. Reverse transcription-polymerase chain reaction (RT-PCR), revealed that all lines (SW480, SW620, DLD-1 and WiDr) expressed mRNA for the Ca(2+)-dependent endothelial (e)NOS, while SW480 cells also expressed the Ca(2+)-dependent neuronal (n)NOS. The mRNA for the Ca(2+)-independent inducible (i)NOS was expressed both by cytokine-stimulated and by unstimulated SW480, SW620 and DLD-1 cells, but none was seen at any time in the WiDr cells. There was, however, little correlation between mRNA expression and enzymic activity based on citrulline and NO2- formation. Thus none of the cell lines exhibited measurable Ca(2+)-dependent NOS activity, while Ca(2+)-independent NOS activity was seen in all but the WiDr cells. Furthermore, DLD-1 cells generated citrulline with resultant NO2- formation only after stimulation with lipopolysaccharide (LPS) and/or cytokines, while SW480 and SW620 did so constitutively. Thus RT-PCR studies indicate that tumour cells of similar epithelial origin display a diverse pattern of NOS gene family expression, and parallel biochemical studies clearly indicate that such expression does not always result in measurable enzymic activity leading to the generation of NO. IMAGES: Nature Publishing Group 1994-11 /pmc/articles/PMC2033551/ /pubmed/7524602 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
Jenkins, D. C.
Charles, I. G.
Baylis, S. A.
Lelchuk, R.
Radomski, M. W.
Moncada, S.
Human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation.
title Human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation.
title_full Human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation.
title_fullStr Human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation.
title_full_unstemmed Human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation.
title_short Human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation.
title_sort human colon cancer cell lines show a diverse pattern of nitric oxide synthase gene expression and nitric oxide generation.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033551/
https://www.ncbi.nlm.nih.gov/pubmed/7524602
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