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Aberrant expression of RAB1A in human tongue cancer
This study was designed to identify specific gene expression changes in tongue squamous cell carcinomas (TSCCs) compared with normal tissues using in-house cDNA microarray that comprised of 2304 full-length cDNAs from a cDNA library prepared from normal oral tissues, primary oral cancers, and oral c...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361773/ https://www.ncbi.nlm.nih.gov/pubmed/15870709 http://dx.doi.org/10.1038/sj.bjc.6602594 |
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author | Shimada, K Uzawa, K Kato, M Endo, Y Shiiba, M Bukawa, H Yokoe, H Seki, N Tanzawa, H |
author_facet | Shimada, K Uzawa, K Kato, M Endo, Y Shiiba, M Bukawa, H Yokoe, H Seki, N Tanzawa, H |
author_sort | Shimada, K |
collection | PubMed |
description | This study was designed to identify specific gene expression changes in tongue squamous cell carcinomas (TSCCs) compared with normal tissues using in-house cDNA microarray that comprised of 2304 full-length cDNAs from a cDNA library prepared from normal oral tissues, primary oral cancers, and oral cancer cell lines. The genes identified by our microarray system were further analysed at the mRNA or protein expression level in a series of clinical samples by real-time quantitative reverse transcriptase–polymerase chain reaction (qRT–PCR) analysis and imuunohositochemistry. The microarray analysis identified a total of 16 genes that were significantly upregulated in common among four TSCC specimens. Consistent with the results of the microarray, increased mRNA levels of selected genes with known molecular functions were found in the four TSCCs. Among genes identified, Rab1a, a member of the Ras oncogene family, was further analysed for its protein expression in 54 TSCCs and 13 premalignant lesions. We found a high prevalence of Rab1A-overexpression not only in TSCCs (98%) but also in premalignant lesions (93%). Thus, our results suggest that rapid characterisation of the target gene(s) for TSCCs can be accomplished using our in-house cDNA microarray analysis combined with the qRT–PCR and immunohistochemistry, and that the Rab1A is a potential biomarker of tongue carcinogenesis. |
format | Text |
id | pubmed-2361773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23617732009-09-10 Aberrant expression of RAB1A in human tongue cancer Shimada, K Uzawa, K Kato, M Endo, Y Shiiba, M Bukawa, H Yokoe, H Seki, N Tanzawa, H Br J Cancer Molecular Diagnostics This study was designed to identify specific gene expression changes in tongue squamous cell carcinomas (TSCCs) compared with normal tissues using in-house cDNA microarray that comprised of 2304 full-length cDNAs from a cDNA library prepared from normal oral tissues, primary oral cancers, and oral cancer cell lines. The genes identified by our microarray system were further analysed at the mRNA or protein expression level in a series of clinical samples by real-time quantitative reverse transcriptase–polymerase chain reaction (qRT–PCR) analysis and imuunohositochemistry. The microarray analysis identified a total of 16 genes that were significantly upregulated in common among four TSCC specimens. Consistent with the results of the microarray, increased mRNA levels of selected genes with known molecular functions were found in the four TSCCs. Among genes identified, Rab1a, a member of the Ras oncogene family, was further analysed for its protein expression in 54 TSCCs and 13 premalignant lesions. We found a high prevalence of Rab1A-overexpression not only in TSCCs (98%) but also in premalignant lesions (93%). Thus, our results suggest that rapid characterisation of the target gene(s) for TSCCs can be accomplished using our in-house cDNA microarray analysis combined with the qRT–PCR and immunohistochemistry, and that the Rab1A is a potential biomarker of tongue carcinogenesis. Nature Publishing Group 2005-05-23 2005-05-03 /pmc/articles/PMC2361773/ /pubmed/15870709 http://dx.doi.org/10.1038/sj.bjc.6602594 Text en Copyright © 2005 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 Shimada, K Uzawa, K Kato, M Endo, Y Shiiba, M Bukawa, H Yokoe, H Seki, N Tanzawa, H Aberrant expression of RAB1A in human tongue cancer |
title | Aberrant expression of RAB1A in human tongue cancer |
title_full | Aberrant expression of RAB1A in human tongue cancer |
title_fullStr | Aberrant expression of RAB1A in human tongue cancer |
title_full_unstemmed | Aberrant expression of RAB1A in human tongue cancer |
title_short | Aberrant expression of RAB1A in human tongue cancer |
title_sort | aberrant expression of rab1a in human tongue cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361773/ https://www.ncbi.nlm.nih.gov/pubmed/15870709 http://dx.doi.org/10.1038/sj.bjc.6602594 |
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