Cargando…
Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk
Over the past 20 years, aberrant crypt foci (ACF) have emerged as potential precursors and biomarkers for colorectal cancer (CRC). However, data regarding their molecular pathogenesis, as well as their endoscopic and histological identification, remain inconsistent. METHODS: A wide cohort of ACF fro...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613864/ https://www.ncbi.nlm.nih.gov/pubmed/31136360 http://dx.doi.org/10.14309/ctg.0000000000000047 |
_version_ | 1783433099792613376 |
---|---|
author | Quintanilla, Isabel López-Cerón, María Jimeno, Mireya Cuatrecasas, Miriam Zabalza, Michel Moreira, Leticia Alonso, Virginia Rodríguez de Miguel, Cristina Muñoz, Jennifer Castellvi-Bel, Sergi Llach, Josep Castells, Antoni Balaguer, Francesc Camps, Jordi Pellisé, Maria |
author_facet | Quintanilla, Isabel López-Cerón, María Jimeno, Mireya Cuatrecasas, Miriam Zabalza, Michel Moreira, Leticia Alonso, Virginia Rodríguez de Miguel, Cristina Muñoz, Jennifer Castellvi-Bel, Sergi Llach, Josep Castells, Antoni Balaguer, Francesc Camps, Jordi Pellisé, Maria |
author_sort | Quintanilla, Isabel |
collection | PubMed |
description | Over the past 20 years, aberrant crypt foci (ACF) have emerged as potential precursors and biomarkers for colorectal cancer (CRC). However, data regarding their molecular pathogenesis, as well as their endoscopic and histological identification, remain inconsistent. METHODS: A wide cohort of ACF from 100 control subjects and 100 case patients, including patients with adenoma and CRC, were characterized for endoscopic, morphologic, and molecular features. RESULTS: We observed that among all the endoscopic features evaluated, only the number of large ACF correlated with CRC risk (P = 0.003), whereas the histological classification, as assessed by 2 different pathologists, was inconsistent and did not differ between control and case patients. Moreover, only a few APC and BRAF mutations and no microsatellite instability were detected in our samples. KRAS mutations were detected in 16.3% of ACF samples, which also exhibited increased MGMT hypermethylation. However, none of those events were found to be predictive of CRC risk. DISCUSSION: Although ACF might be preneoplastic lesions of the colon, they are not suitable biomarkers for assessing CRC progression. |
format | Online Article Text |
id | pubmed-6613864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-66138642019-07-24 Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk Quintanilla, Isabel López-Cerón, María Jimeno, Mireya Cuatrecasas, Miriam Zabalza, Michel Moreira, Leticia Alonso, Virginia Rodríguez de Miguel, Cristina Muñoz, Jennifer Castellvi-Bel, Sergi Llach, Josep Castells, Antoni Balaguer, Francesc Camps, Jordi Pellisé, Maria Clin Transl Gastroenterol Article Over the past 20 years, aberrant crypt foci (ACF) have emerged as potential precursors and biomarkers for colorectal cancer (CRC). However, data regarding their molecular pathogenesis, as well as their endoscopic and histological identification, remain inconsistent. METHODS: A wide cohort of ACF from 100 control subjects and 100 case patients, including patients with adenoma and CRC, were characterized for endoscopic, morphologic, and molecular features. RESULTS: We observed that among all the endoscopic features evaluated, only the number of large ACF correlated with CRC risk (P = 0.003), whereas the histological classification, as assessed by 2 different pathologists, was inconsistent and did not differ between control and case patients. Moreover, only a few APC and BRAF mutations and no microsatellite instability were detected in our samples. KRAS mutations were detected in 16.3% of ACF samples, which also exhibited increased MGMT hypermethylation. However, none of those events were found to be predictive of CRC risk. DISCUSSION: Although ACF might be preneoplastic lesions of the colon, they are not suitable biomarkers for assessing CRC progression. Wolters Kluwer 2019-05-15 /pmc/articles/PMC6613864/ /pubmed/31136360 http://dx.doi.org/10.14309/ctg.0000000000000047 Text en © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://CreativeCommonsAttribution-NonCommercial-NoDerivativesLicense4.0(CCBY-NC-ND)) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Quintanilla, Isabel López-Cerón, María Jimeno, Mireya Cuatrecasas, Miriam Zabalza, Michel Moreira, Leticia Alonso, Virginia Rodríguez de Miguel, Cristina Muñoz, Jennifer Castellvi-Bel, Sergi Llach, Josep Castells, Antoni Balaguer, Francesc Camps, Jordi Pellisé, Maria Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk |
title | Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk |
title_full | Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk |
title_fullStr | Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk |
title_full_unstemmed | Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk |
title_short | Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk |
title_sort | rectal aberrant crypt foci in humans are not surrogate markers for colorectal cancer risk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613864/ https://www.ncbi.nlm.nih.gov/pubmed/31136360 http://dx.doi.org/10.14309/ctg.0000000000000047 |
work_keys_str_mv | AT quintanillaisabel rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT lopezceronmaria rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT jimenomireya rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT cuatrecasasmiriam rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT zabalzamichel rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT moreiraleticia rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT alonsovirginia rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT rodriguezdemiguelcristina rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT munozjennifer rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT castellvibelsergi rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT llachjosep rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT castellsantoni rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT balaguerfrancesc rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT campsjordi rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk AT pellisemaria rectalaberrantcryptfociinhumansarenotsurrogatemarkersforcolorectalcancerrisk |