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LRIG1 expression and colorectal cancer prognosis
BACKGROUND: To make the right treatment decisions about colorectal cancer (CRC) patients reliable predictive and prognostic data are needed. However, in many cases this data is not enough. Some studies suggest that LRIG1 gene (leucine-rich repeats and immunoglobulin-like domains1) has prognostic imp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814534/ https://www.ncbi.nlm.nih.gov/pubmed/33461538 http://dx.doi.org/10.1186/s12920-020-00846-2 |
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author | Bakherad, Maryam Salimi, Mahdieh Angaji, Seyed Abdolhamid Mahjoubi, Frouzandeh Majidizadeh, Tayebeh |
author_facet | Bakherad, Maryam Salimi, Mahdieh Angaji, Seyed Abdolhamid Mahjoubi, Frouzandeh Majidizadeh, Tayebeh |
author_sort | Bakherad, Maryam |
collection | PubMed |
description | BACKGROUND: To make the right treatment decisions about colorectal cancer (CRC) patients reliable predictive and prognostic data are needed. However, in many cases this data is not enough. Some studies suggest that LRIG1 gene (leucine-rich repeats and immunoglobulin-like domains1) has prognostic implications in different kinds of cancers. METHODS: One hundred and two patients with colorectal cancer were retrospectively analyzed for LRIG1 expression at both mRNA and protein levels. SYBR Green Real-Time RT-PCR technique was used for mRNA expression analyses and Glyceraldehyde-3-Phosphate Dehydrogenase gene (GAPDH) was considered as a reference gene for data normalization. LRIG1 protein expression was analyzed using Immunohistochemistry. Additionally, appropriate statistic analyses were used to assess the expression of LRIG1 in test and control groups. The prognostic significance of LRIG1 expression was analyzed using the univariate and multivariate analyses. RESULTS: The data revealed that the expression of LRIG1 in both mRNA and protein levels was down regulated in colorectal tumor tissues (P < 0.01) but is not clinically relevant prognostic indicator in CRC. CONCLUSIONS: Therefore, it is suggested that LRIG1 expression analyses may not be considered as an important issue when making informed and individualized clinical decisions regarding the management of colorectal cancer patients. |
format | Online Article Text |
id | pubmed-7814534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78145342021-01-19 LRIG1 expression and colorectal cancer prognosis Bakherad, Maryam Salimi, Mahdieh Angaji, Seyed Abdolhamid Mahjoubi, Frouzandeh Majidizadeh, Tayebeh BMC Med Genomics Research Article BACKGROUND: To make the right treatment decisions about colorectal cancer (CRC) patients reliable predictive and prognostic data are needed. However, in many cases this data is not enough. Some studies suggest that LRIG1 gene (leucine-rich repeats and immunoglobulin-like domains1) has prognostic implications in different kinds of cancers. METHODS: One hundred and two patients with colorectal cancer were retrospectively analyzed for LRIG1 expression at both mRNA and protein levels. SYBR Green Real-Time RT-PCR technique was used for mRNA expression analyses and Glyceraldehyde-3-Phosphate Dehydrogenase gene (GAPDH) was considered as a reference gene for data normalization. LRIG1 protein expression was analyzed using Immunohistochemistry. Additionally, appropriate statistic analyses were used to assess the expression of LRIG1 in test and control groups. The prognostic significance of LRIG1 expression was analyzed using the univariate and multivariate analyses. RESULTS: The data revealed that the expression of LRIG1 in both mRNA and protein levels was down regulated in colorectal tumor tissues (P < 0.01) but is not clinically relevant prognostic indicator in CRC. CONCLUSIONS: Therefore, it is suggested that LRIG1 expression analyses may not be considered as an important issue when making informed and individualized clinical decisions regarding the management of colorectal cancer patients. BioMed Central 2021-01-18 /pmc/articles/PMC7814534/ /pubmed/33461538 http://dx.doi.org/10.1186/s12920-020-00846-2 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Bakherad, Maryam Salimi, Mahdieh Angaji, Seyed Abdolhamid Mahjoubi, Frouzandeh Majidizadeh, Tayebeh LRIG1 expression and colorectal cancer prognosis |
title | LRIG1 expression and colorectal cancer prognosis |
title_full | LRIG1 expression and colorectal cancer prognosis |
title_fullStr | LRIG1 expression and colorectal cancer prognosis |
title_full_unstemmed | LRIG1 expression and colorectal cancer prognosis |
title_short | LRIG1 expression and colorectal cancer prognosis |
title_sort | lrig1 expression and colorectal cancer prognosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814534/ https://www.ncbi.nlm.nih.gov/pubmed/33461538 http://dx.doi.org/10.1186/s12920-020-00846-2 |
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