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‘Desperate house genes’: the dramatic example of hypoxia

BACKGROUND: Microenvironmental conditions in normal or tumour tissues and cell lines may interfere on further biological analysis. To evaluate transcript variations carefully, it is common to use stable housekeeping genes (HKG) to normalise quantitative microarrays or real-time polymerase chain reac...

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Autores principales: Caradec, J, Sirab, N, Keumeugni, C, Moutereau, S, Chimingqi, M, Matar, C, Revaud, D, Bah, M, Manivet, P, Conti, M, Loric, S
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2844028/
https://www.ncbi.nlm.nih.gov/pubmed/20179706
http://dx.doi.org/10.1038/sj.bjc.6605573
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author Caradec, J
Sirab, N
Keumeugni, C
Moutereau, S
Chimingqi, M
Matar, C
Revaud, D
Bah, M
Manivet, P
Conti, M
Loric, S
author_facet Caradec, J
Sirab, N
Keumeugni, C
Moutereau, S
Chimingqi, M
Matar, C
Revaud, D
Bah, M
Manivet, P
Conti, M
Loric, S
author_sort Caradec, J
collection PubMed
description BACKGROUND: Microenvironmental conditions in normal or tumour tissues and cell lines may interfere on further biological analysis. To evaluate transcript variations carefully, it is common to use stable housekeeping genes (HKG) to normalise quantitative microarrays or real-time polymerase chain reaction results. However, recent studies argue that HKG fluctuate according to tissues and treatments. So, as an example of HKG variation under an array of conditions that are common in the cancer field, we evaluate whether hypoxia could have an impact on HKG expression. METHODS: Expression of 10 commonly used HKG was measured on four cell lines treated with four oxygen concentrations (from 1 to 20%). RESULTS: Large variations of HKG transcripts were observed in hypoxic conditions and differ along with the cell line and the oxygen concentration. To elect the most stable HKG, we compared the three statistical means based either on PCR cycle threshold coefficient of variation calculation or two specifically dedicated software. Nevertheless, the best HKG dramatically differs according to the statistical method used. Moreover, using, as a reference, absolute quantification of a target gene (here the proteinase activating receptor gene 1 (PAR1) gene), we show that the conclusions raised about PAR1 variation in hypoxia can totally diverge according to the selected HKG used for normalisation. CONCLUSION: The choice of a valid HKG will determine the relevance of the results that will be further interpreted, and so it should be seriously considered. The results of our study confirm unambiguously that HKG variations must be precisely and systematically determined before any experiment for each situation, to obtain reliable normalised results in the experimental setting that has been designed. Indeed, such assay design, functional for all in vitro systems, should be carefully evaluated before any extension to other experimental models including in vivo ones.
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spelling pubmed-28440282011-03-16 ‘Desperate house genes’: the dramatic example of hypoxia Caradec, J Sirab, N Keumeugni, C Moutereau, S Chimingqi, M Matar, C Revaud, D Bah, M Manivet, P Conti, M Loric, S Br J Cancer Molecular Diagnostics BACKGROUND: Microenvironmental conditions in normal or tumour tissues and cell lines may interfere on further biological analysis. To evaluate transcript variations carefully, it is common to use stable housekeeping genes (HKG) to normalise quantitative microarrays or real-time polymerase chain reaction results. However, recent studies argue that HKG fluctuate according to tissues and treatments. So, as an example of HKG variation under an array of conditions that are common in the cancer field, we evaluate whether hypoxia could have an impact on HKG expression. METHODS: Expression of 10 commonly used HKG was measured on four cell lines treated with four oxygen concentrations (from 1 to 20%). RESULTS: Large variations of HKG transcripts were observed in hypoxic conditions and differ along with the cell line and the oxygen concentration. To elect the most stable HKG, we compared the three statistical means based either on PCR cycle threshold coefficient of variation calculation or two specifically dedicated software. Nevertheless, the best HKG dramatically differs according to the statistical method used. Moreover, using, as a reference, absolute quantification of a target gene (here the proteinase activating receptor gene 1 (PAR1) gene), we show that the conclusions raised about PAR1 variation in hypoxia can totally diverge according to the selected HKG used for normalisation. CONCLUSION: The choice of a valid HKG will determine the relevance of the results that will be further interpreted, and so it should be seriously considered. The results of our study confirm unambiguously that HKG variations must be precisely and systematically determined before any experiment for each situation, to obtain reliable normalised results in the experimental setting that has been designed. Indeed, such assay design, functional for all in vitro systems, should be carefully evaluated before any extension to other experimental models including in vivo ones. Nature Publishing Group 2010-03-16 2010-02-23 /pmc/articles/PMC2844028/ /pubmed/20179706 http://dx.doi.org/10.1038/sj.bjc.6605573 Text en Copyright © 2010 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 Diagnostics
Caradec, J
Sirab, N
Keumeugni, C
Moutereau, S
Chimingqi, M
Matar, C
Revaud, D
Bah, M
Manivet, P
Conti, M
Loric, S
‘Desperate house genes’: the dramatic example of hypoxia
title ‘Desperate house genes’: the dramatic example of hypoxia
title_full ‘Desperate house genes’: the dramatic example of hypoxia
title_fullStr ‘Desperate house genes’: the dramatic example of hypoxia
title_full_unstemmed ‘Desperate house genes’: the dramatic example of hypoxia
title_short ‘Desperate house genes’: the dramatic example of hypoxia
title_sort ‘desperate house genes’: the dramatic example of hypoxia
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2844028/
https://www.ncbi.nlm.nih.gov/pubmed/20179706
http://dx.doi.org/10.1038/sj.bjc.6605573
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