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Clinical significance of the reduced expression of G protein gamma 7 (GNG7) in oesophageal cancer
We previously cloned human G protein gamma 7 (GNG7) and demonstrated that it was downregulated in gastrointestinal cancer. The significance of GNG7 expression in oesophageal cancer is unknown. TaqMan quantitative real-time PCR was performed to determine the clinical significance of GNG7 expression i...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361448/ https://www.ncbi.nlm.nih.gov/pubmed/18219292 http://dx.doi.org/10.1038/sj.bjc.6604124 |
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author | Ohta, M Mimori, K Fukuyoshi, Y Kita, Y Motoyama, K Yamashita, K Ishii, H Inoue, H Mori, M |
author_facet | Ohta, M Mimori, K Fukuyoshi, Y Kita, Y Motoyama, K Yamashita, K Ishii, H Inoue, H Mori, M |
author_sort | Ohta, M |
collection | PubMed |
description | We previously cloned human G protein gamma 7 (GNG7) and demonstrated that it was downregulated in gastrointestinal cancer. The significance of GNG7 expression in oesophageal cancer is unknown. TaqMan quantitative real-time PCR was performed to determine the clinical significance of GNG7 expression in 55 cases of oesophageal cancer. Furthermore, GNG7-transfected oesophageal cancer cells were analysed in laboratory studies at genomic and epigenetic levels. Twenty-seven patients with low GNG7 expression showed significantly poorer survival than did 28 patients with high expression (P<0.05). Tumours with low GNG7 expression invaded deeper than those with high GNG7 expression (P<0.05), both in vivo and in vitro. Eight tumours retained GNG7 expression, and they did not show either promoter hypermethylation or loss of heterozygosity (LOH). In 38 tumours with GNG7 suppression, 22 (57%) showed either LOH or promoter hypermethylation. In addition, GNG7 expression was significantly associated with the presence of miR328 in oesophageal cancer cell lines, which suggests that this microRNA might be a regulator of GNG7 expression. GNG7 suppression represents a new prognostic indicator in cases of oesophageal cancer. GNG7 might be suppressed by LOH and promoter hypermethylation or by microRNA. |
format | Text |
id | pubmed-2361448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23614482009-09-10 Clinical significance of the reduced expression of G protein gamma 7 (GNG7) in oesophageal cancer Ohta, M Mimori, K Fukuyoshi, Y Kita, Y Motoyama, K Yamashita, K Ishii, H Inoue, H Mori, M Br J Cancer Molecular Diagnostics We previously cloned human G protein gamma 7 (GNG7) and demonstrated that it was downregulated in gastrointestinal cancer. The significance of GNG7 expression in oesophageal cancer is unknown. TaqMan quantitative real-time PCR was performed to determine the clinical significance of GNG7 expression in 55 cases of oesophageal cancer. Furthermore, GNG7-transfected oesophageal cancer cells were analysed in laboratory studies at genomic and epigenetic levels. Twenty-seven patients with low GNG7 expression showed significantly poorer survival than did 28 patients with high expression (P<0.05). Tumours with low GNG7 expression invaded deeper than those with high GNG7 expression (P<0.05), both in vivo and in vitro. Eight tumours retained GNG7 expression, and they did not show either promoter hypermethylation or loss of heterozygosity (LOH). In 38 tumours with GNG7 suppression, 22 (57%) showed either LOH or promoter hypermethylation. In addition, GNG7 expression was significantly associated with the presence of miR328 in oesophageal cancer cell lines, which suggests that this microRNA might be a regulator of GNG7 expression. GNG7 suppression represents a new prognostic indicator in cases of oesophageal cancer. GNG7 might be suppressed by LOH and promoter hypermethylation or by microRNA. Nature Publishing Group 2008-01-29 2008-01-22 /pmc/articles/PMC2361448/ /pubmed/18219292 http://dx.doi.org/10.1038/sj.bjc.6604124 Text en Copyright © 2008 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 Ohta, M Mimori, K Fukuyoshi, Y Kita, Y Motoyama, K Yamashita, K Ishii, H Inoue, H Mori, M Clinical significance of the reduced expression of G protein gamma 7 (GNG7) in oesophageal cancer |
title | Clinical significance of the reduced expression of G protein gamma 7 (GNG7) in oesophageal cancer |
title_full | Clinical significance of the reduced expression of G protein gamma 7 (GNG7) in oesophageal cancer |
title_fullStr | Clinical significance of the reduced expression of G protein gamma 7 (GNG7) in oesophageal cancer |
title_full_unstemmed | Clinical significance of the reduced expression of G protein gamma 7 (GNG7) in oesophageal cancer |
title_short | Clinical significance of the reduced expression of G protein gamma 7 (GNG7) in oesophageal cancer |
title_sort | clinical significance of the reduced expression of g protein gamma 7 (gng7) in oesophageal cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361448/ https://www.ncbi.nlm.nih.gov/pubmed/18219292 http://dx.doi.org/10.1038/sj.bjc.6604124 |
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