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Reference gene selection for head and neck squamous cell carcinoma gene expression studies
BACKGROUND: It is no longer adequate to choose reference genes blindly. We present the first study that defines the suitability of 12 reference genes commonly used in cancer studies (ACT, ALAS, B2M, GAPDH, HMBS, HPRT, KALPHA, RPS18, RPL27, RPS29, SHAD and TBP) for the normalization of quantitative e...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729078/ https://www.ncbi.nlm.nih.gov/pubmed/19650912 http://dx.doi.org/10.1186/1471-2199-10-78 |
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author | Lallemant, Benjamin Evrard, Alexandre Combescure, Christophe Chapuis, Heliette Chambon, Guillaume Raynal, Caroline Reynaud, Christophe Sabra, Omar Joubert, Dominique Hollande, Frédéric Lallemant, Jean-Gabriel Lumbroso, Serge Brouillet, Jean-Paul |
author_facet | Lallemant, Benjamin Evrard, Alexandre Combescure, Christophe Chapuis, Heliette Chambon, Guillaume Raynal, Caroline Reynaud, Christophe Sabra, Omar Joubert, Dominique Hollande, Frédéric Lallemant, Jean-Gabriel Lumbroso, Serge Brouillet, Jean-Paul |
author_sort | Lallemant, Benjamin |
collection | PubMed |
description | BACKGROUND: It is no longer adequate to choose reference genes blindly. We present the first study that defines the suitability of 12 reference genes commonly used in cancer studies (ACT, ALAS, B2M, GAPDH, HMBS, HPRT, KALPHA, RPS18, RPL27, RPS29, SHAD and TBP) for the normalization of quantitative expression data in the field of head and neck squamous cell carcinoma (HNSCC). RESULTS: Raw expression levels were measured by RT-qPCR in HNSCC and normal matched mucosa of 46 patients. We analyzed the expression stability using geNorm and NormFinder and compared the expression levels between subgroups. In HNSCC and/or normal mucosa, the four best normalization genes were ALAS, GAPDH, RPS18 and SHAD and the most stable combination of two genes was GAPDH-SHAD. We recommend using KALPHA-TBP for the study of T1-T2 tumors, RPL27-SHAD for T3-T4 tumors, KALPHA-SHAD for N0 tumors, and ALAS-TBP for N+ tumors. ACT, B2M, GAPDH, HMBS, HPRT, KALPHA, RPS18, RPS29, SHAD and TBP were slightly misregulated (<1.7-fold) between tumor and normal mucosa but can be used for normalization, depending on the resolution required for the assay. CONCLUSION: In the field of HNSCC, this study will guide researchers in selecting the most appropriate reference genes from among 12 potentially suitable reference genes, depending on the specific setting of their experiments. |
format | Text |
id | pubmed-2729078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27290782009-08-20 Reference gene selection for head and neck squamous cell carcinoma gene expression studies Lallemant, Benjamin Evrard, Alexandre Combescure, Christophe Chapuis, Heliette Chambon, Guillaume Raynal, Caroline Reynaud, Christophe Sabra, Omar Joubert, Dominique Hollande, Frédéric Lallemant, Jean-Gabriel Lumbroso, Serge Brouillet, Jean-Paul BMC Mol Biol Research Article BACKGROUND: It is no longer adequate to choose reference genes blindly. We present the first study that defines the suitability of 12 reference genes commonly used in cancer studies (ACT, ALAS, B2M, GAPDH, HMBS, HPRT, KALPHA, RPS18, RPL27, RPS29, SHAD and TBP) for the normalization of quantitative expression data in the field of head and neck squamous cell carcinoma (HNSCC). RESULTS: Raw expression levels were measured by RT-qPCR in HNSCC and normal matched mucosa of 46 patients. We analyzed the expression stability using geNorm and NormFinder and compared the expression levels between subgroups. In HNSCC and/or normal mucosa, the four best normalization genes were ALAS, GAPDH, RPS18 and SHAD and the most stable combination of two genes was GAPDH-SHAD. We recommend using KALPHA-TBP for the study of T1-T2 tumors, RPL27-SHAD for T3-T4 tumors, KALPHA-SHAD for N0 tumors, and ALAS-TBP for N+ tumors. ACT, B2M, GAPDH, HMBS, HPRT, KALPHA, RPS18, RPS29, SHAD and TBP were slightly misregulated (<1.7-fold) between tumor and normal mucosa but can be used for normalization, depending on the resolution required for the assay. CONCLUSION: In the field of HNSCC, this study will guide researchers in selecting the most appropriate reference genes from among 12 potentially suitable reference genes, depending on the specific setting of their experiments. BioMed Central 2009-08-03 /pmc/articles/PMC2729078/ /pubmed/19650912 http://dx.doi.org/10.1186/1471-2199-10-78 Text en Copyright © 2009 Lallemant et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lallemant, Benjamin Evrard, Alexandre Combescure, Christophe Chapuis, Heliette Chambon, Guillaume Raynal, Caroline Reynaud, Christophe Sabra, Omar Joubert, Dominique Hollande, Frédéric Lallemant, Jean-Gabriel Lumbroso, Serge Brouillet, Jean-Paul Reference gene selection for head and neck squamous cell carcinoma gene expression studies |
title | Reference gene selection for head and neck squamous cell carcinoma gene expression studies |
title_full | Reference gene selection for head and neck squamous cell carcinoma gene expression studies |
title_fullStr | Reference gene selection for head and neck squamous cell carcinoma gene expression studies |
title_full_unstemmed | Reference gene selection for head and neck squamous cell carcinoma gene expression studies |
title_short | Reference gene selection for head and neck squamous cell carcinoma gene expression studies |
title_sort | reference gene selection for head and neck squamous cell carcinoma gene expression studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729078/ https://www.ncbi.nlm.nih.gov/pubmed/19650912 http://dx.doi.org/10.1186/1471-2199-10-78 |
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