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...

Descripción completa

Detalles Bibliográficos
Autores principales: Sussman, Daniel A, Santaolalla, Rebeca, Bejarano, Pablo A, Garcia-Buitrago, Monica T, Perez, Maria T, Abreu, Maria T, Clarke, Jennifer
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