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Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis
BACKGROUND: TRIB3 is a human homologue of Drosophila tribbles. Previous studies have shown that TRIB3 controls the cell growth through ubiquitination-dependent degradation of other proteins, whereas its significance in the prognosis of colorectal cancer (CRC) is not yet fully understood. MATERIALS:...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778541/ https://www.ncbi.nlm.nih.gov/pubmed/19904274 http://dx.doi.org/10.1038/sj.bjc.6605361 |
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author | Miyoshi, N Ishii, H Mimori, K Takatsuno, Y Kim, H Hirose, H Sekimoto, M Doki, Y Mori, M |
author_facet | Miyoshi, N Ishii, H Mimori, K Takatsuno, Y Kim, H Hirose, H Sekimoto, M Doki, Y Mori, M |
author_sort | Miyoshi, N |
collection | PubMed |
description | BACKGROUND: TRIB3 is a human homologue of Drosophila tribbles. Previous studies have shown that TRIB3 controls the cell growth through ubiquitination-dependent degradation of other proteins, whereas its significance in the prognosis of colorectal cancer (CRC) is not yet fully understood. MATERIALS: This study comprised 202 patients who underwent surgery for CRC, as well as 22 cell lines derived from human gastrointestinal cancer. The correlation of gene expression with clinical parameters in patients was assessed. The biological significance was evaluated by knockdown experiments in seven colorectal cancer cell lines. RESULTS: A total of 20 cancer cell lines (90.9%) expressed the TRIB3 gene. The assessment in surgical specimens indicated that the gene expression was significantly higher in the cancerous region than in the marginal non-cancerous region. Patients with high TRIB3 expression were statistically susceptible to a recurrence of the disease, and showed poorer overall survival than those with low expression. The assessment of TRIB3 knockdown in five cell lines showed that small interfering RNA (siRNA) inhibition resulted in a statistically significant reduction in cell growth. CONCLUSION: These data strongly suggest the usefulness of TRIB3 as a marker for predicting the prognosis of CRC patients, showing a basis for the development of effective treatments for CRC. |
format | Text |
id | pubmed-2778541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-27785412010-11-17 Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis Miyoshi, N Ishii, H Mimori, K Takatsuno, Y Kim, H Hirose, H Sekimoto, M Doki, Y Mori, M Br J Cancer Clinical Study BACKGROUND: TRIB3 is a human homologue of Drosophila tribbles. Previous studies have shown that TRIB3 controls the cell growth through ubiquitination-dependent degradation of other proteins, whereas its significance in the prognosis of colorectal cancer (CRC) is not yet fully understood. MATERIALS: This study comprised 202 patients who underwent surgery for CRC, as well as 22 cell lines derived from human gastrointestinal cancer. The correlation of gene expression with clinical parameters in patients was assessed. The biological significance was evaluated by knockdown experiments in seven colorectal cancer cell lines. RESULTS: A total of 20 cancer cell lines (90.9%) expressed the TRIB3 gene. The assessment in surgical specimens indicated that the gene expression was significantly higher in the cancerous region than in the marginal non-cancerous region. Patients with high TRIB3 expression were statistically susceptible to a recurrence of the disease, and showed poorer overall survival than those with low expression. The assessment of TRIB3 knockdown in five cell lines showed that small interfering RNA (siRNA) inhibition resulted in a statistically significant reduction in cell growth. CONCLUSION: These data strongly suggest the usefulness of TRIB3 as a marker for predicting the prognosis of CRC patients, showing a basis for the development of effective treatments for CRC. Nature Publishing Group 2009-11-17 2009-11-10 /pmc/articles/PMC2778541/ /pubmed/19904274 http://dx.doi.org/10.1038/sj.bjc.6605361 Text en Copyright © 2009 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 | Clinical Study Miyoshi, N Ishii, H Mimori, K Takatsuno, Y Kim, H Hirose, H Sekimoto, M Doki, Y Mori, M Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis |
title | Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis |
title_full | Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis |
title_fullStr | Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis |
title_full_unstemmed | Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis |
title_short | Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis |
title_sort | abnormal expression of trib3 in colorectal cancer: a novel marker for prognosis |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778541/ https://www.ncbi.nlm.nih.gov/pubmed/19904274 http://dx.doi.org/10.1038/sj.bjc.6605361 |
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