Cargando…
In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer
BACKGROUND: Inflammation increases the risk of colorectal cancer (CRC). We and others have described a role for TLR4, the receptor for LPS, in colon cancer. To explore the relationships between TLR4 expression and CRC, we combined the strength of transcriptome array data and immunohistochemical (IHC...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046523/ https://www.ncbi.nlm.nih.gov/pubmed/24887394 http://dx.doi.org/10.1186/1756-9966-33-45 |
_version_ | 1782480275439091712 |
---|---|
author | Sussman, Daniel A Santaolalla, Rebeca Bejarano, Pablo A Garcia-Buitrago, Monica T Perez, Maria T Abreu, Maria T Clarke, Jennifer |
author_facet | Sussman, Daniel A Santaolalla, Rebeca Bejarano, Pablo A Garcia-Buitrago, Monica T Perez, Maria T Abreu, Maria T Clarke, Jennifer |
author_sort | Sussman, Daniel A |
collection | PubMed |
description | BACKGROUND: Inflammation increases the risk of colorectal cancer (CRC). We and others have described a role for TLR4, the receptor for LPS, in colon cancer. To explore the relationships between TLR4 expression and CRC, we combined the strength of transcriptome array data and immunohistochemical (IHC) staining. METHODS: TLR4 signal intensity was scored in the stromal and epithelial compartments. Detection of differential expression between conditions of interest was performed using linear models, Cox proportional hazards models, and empirical Bayes methods. RESULTS: A strong association between TLR4 expression and survival was noted, though a dichotomous relationship between survival and specific TLR4 transcripts was observed. Increasing TLR4 expression was seen with advancing tumor stage and was also over-expressed in some adenomas. IHC staining confirmed the positive relationship between TLR4 staining score in the CRC tumor stroma and epithelium with tumor stage, with up to 47% of colon cancer stroma positive for TLR4 staining. Increased TLR4 expression by IHC was also marginally associated with decreased survival. We now also describe that pericryptal myofibroblasts are responsible for a portion of the TLR4 stromal staining. CONCLUSIONS: Increased TLR4 expression occurs early in colonic neoplasia. TLR4 is associated with the important cancer-related outcomes of survival and stage. |
format | Online Article Text |
id | pubmed-4046523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40465232014-06-06 In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer Sussman, Daniel A Santaolalla, Rebeca Bejarano, Pablo A Garcia-Buitrago, Monica T Perez, Maria T Abreu, Maria T Clarke, Jennifer J Exp Clin Cancer Res Research BACKGROUND: Inflammation increases the risk of colorectal cancer (CRC). We and others have described a role for TLR4, the receptor for LPS, in colon cancer. To explore the relationships between TLR4 expression and CRC, we combined the strength of transcriptome array data and immunohistochemical (IHC) staining. METHODS: TLR4 signal intensity was scored in the stromal and epithelial compartments. Detection of differential expression between conditions of interest was performed using linear models, Cox proportional hazards models, and empirical Bayes methods. RESULTS: A strong association between TLR4 expression and survival was noted, though a dichotomous relationship between survival and specific TLR4 transcripts was observed. Increasing TLR4 expression was seen with advancing tumor stage and was also over-expressed in some adenomas. IHC staining confirmed the positive relationship between TLR4 staining score in the CRC tumor stroma and epithelium with tumor stage, with up to 47% of colon cancer stroma positive for TLR4 staining. Increased TLR4 expression by IHC was also marginally associated with decreased survival. We now also describe that pericryptal myofibroblasts are responsible for a portion of the TLR4 stromal staining. CONCLUSIONS: Increased TLR4 expression occurs early in colonic neoplasia. TLR4 is associated with the important cancer-related outcomes of survival and stage. BioMed Central 2014-05-22 /pmc/articles/PMC4046523/ /pubmed/24887394 http://dx.doi.org/10.1186/1756-9966-33-45 Text en Copyright © 2014 Sussman 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 credited. 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. |
spellingShingle | Research Sussman, Daniel A Santaolalla, Rebeca Bejarano, Pablo A Garcia-Buitrago, Monica T Perez, Maria T Abreu, Maria T Clarke, Jennifer In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer |
title | In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer |
title_full | In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer |
title_fullStr | In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer |
title_full_unstemmed | In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer |
title_short | In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer |
title_sort | in silico and ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046523/ https://www.ncbi.nlm.nih.gov/pubmed/24887394 http://dx.doi.org/10.1186/1756-9966-33-45 |
work_keys_str_mv | AT sussmandaniela insilicoandexvivoapproachesidentifyarolefortolllikereceptor4incolorectalcancer AT santaolallarebeca insilicoandexvivoapproachesidentifyarolefortolllikereceptor4incolorectalcancer AT bejaranopabloa insilicoandexvivoapproachesidentifyarolefortolllikereceptor4incolorectalcancer AT garciabuitragomonicat insilicoandexvivoapproachesidentifyarolefortolllikereceptor4incolorectalcancer AT perezmariat insilicoandexvivoapproachesidentifyarolefortolllikereceptor4incolorectalcancer AT abreumariat insilicoandexvivoapproachesidentifyarolefortolllikereceptor4incolorectalcancer AT clarkejennifer insilicoandexvivoapproachesidentifyarolefortolllikereceptor4incolorectalcancer |