Cargando…

Commitment of Scaffold Proteins in the Onco-Biology of Human Colorectal Cancer and Liver Metastases after Oxaliplatin-Based Chemotherapy

Scaffold proteins play pivotal roles in the regulation of signaling pathways, integrating external and internal stimuli to various cellular outputs. We report the pattern of cellular and subcellular expression of scaffoldins angiomotin-like 2 (AmotL2), FK506 binding protein 5 (FKBP51) and IQ motif c...

Descripción completa

Detalles Bibliográficos
Autores principales: Rotoli, Deborah, Morales, Manuel, Ávila, Julio, Maeso, María del Carmen, García, María del Pino, Mobasheri, Ali, Martín-Vasallo, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412470/
https://www.ncbi.nlm.nih.gov/pubmed/28441737
http://dx.doi.org/10.3390/ijms18040891
_version_ 1783233010950209536
author Rotoli, Deborah
Morales, Manuel
Ávila, Julio
Maeso, María del Carmen
García, María del Pino
Mobasheri, Ali
Martín-Vasallo, Pablo
author_facet Rotoli, Deborah
Morales, Manuel
Ávila, Julio
Maeso, María del Carmen
García, María del Pino
Mobasheri, Ali
Martín-Vasallo, Pablo
author_sort Rotoli, Deborah
collection PubMed
description Scaffold proteins play pivotal roles in the regulation of signaling pathways, integrating external and internal stimuli to various cellular outputs. We report the pattern of cellular and subcellular expression of scaffoldins angiomotin-like 2 (AmotL2), FK506 binding protein 5 (FKBP51) and IQ motif containing GTPase-activating protein 1 (IQGAP1) in colorectal cancer (CRC) and metastases in liver resected after oxaliplatin-based chemotherapy (CT). Positive immunostaining for the three scaffoldins was found in most cells in healthy colon, tumor, healthy liver and metastasized liver. The patterns of expression of AmotL2, FKBP51 and IQGAP1 show the greatest variability in immune system cells and neurons and glia cells and the least in blood vessel cells. The simultaneous subcellular localization in tumor cells and other cell types within the tumor suggest an involvement of these three scaffoldins in cancer biology, including a role in Epithelial Mesenchymal Transition. The display in differential localization and quantitative expression of AmotL2, FKBP51, and IQGAP1 could be used as biomarkers for more accurate tumor staging and as potential targets for anti-cancer therapeutics by blocking or slowing down their interconnecting functions. Tough further research needs to be done in order to improve these assessments.
format Online
Article
Text
id pubmed-5412470
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-54124702017-05-05 Commitment of Scaffold Proteins in the Onco-Biology of Human Colorectal Cancer and Liver Metastases after Oxaliplatin-Based Chemotherapy Rotoli, Deborah Morales, Manuel Ávila, Julio Maeso, María del Carmen García, María del Pino Mobasheri, Ali Martín-Vasallo, Pablo Int J Mol Sci Article Scaffold proteins play pivotal roles in the regulation of signaling pathways, integrating external and internal stimuli to various cellular outputs. We report the pattern of cellular and subcellular expression of scaffoldins angiomotin-like 2 (AmotL2), FK506 binding protein 5 (FKBP51) and IQ motif containing GTPase-activating protein 1 (IQGAP1) in colorectal cancer (CRC) and metastases in liver resected after oxaliplatin-based chemotherapy (CT). Positive immunostaining for the three scaffoldins was found in most cells in healthy colon, tumor, healthy liver and metastasized liver. The patterns of expression of AmotL2, FKBP51 and IQGAP1 show the greatest variability in immune system cells and neurons and glia cells and the least in blood vessel cells. The simultaneous subcellular localization in tumor cells and other cell types within the tumor suggest an involvement of these three scaffoldins in cancer biology, including a role in Epithelial Mesenchymal Transition. The display in differential localization and quantitative expression of AmotL2, FKBP51, and IQGAP1 could be used as biomarkers for more accurate tumor staging and as potential targets for anti-cancer therapeutics by blocking or slowing down their interconnecting functions. Tough further research needs to be done in order to improve these assessments. MDPI 2017-04-22 /pmc/articles/PMC5412470/ /pubmed/28441737 http://dx.doi.org/10.3390/ijms18040891 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rotoli, Deborah
Morales, Manuel
Ávila, Julio
Maeso, María del Carmen
García, María del Pino
Mobasheri, Ali
Martín-Vasallo, Pablo
Commitment of Scaffold Proteins in the Onco-Biology of Human Colorectal Cancer and Liver Metastases after Oxaliplatin-Based Chemotherapy
title Commitment of Scaffold Proteins in the Onco-Biology of Human Colorectal Cancer and Liver Metastases after Oxaliplatin-Based Chemotherapy
title_full Commitment of Scaffold Proteins in the Onco-Biology of Human Colorectal Cancer and Liver Metastases after Oxaliplatin-Based Chemotherapy
title_fullStr Commitment of Scaffold Proteins in the Onco-Biology of Human Colorectal Cancer and Liver Metastases after Oxaliplatin-Based Chemotherapy
title_full_unstemmed Commitment of Scaffold Proteins in the Onco-Biology of Human Colorectal Cancer and Liver Metastases after Oxaliplatin-Based Chemotherapy
title_short Commitment of Scaffold Proteins in the Onco-Biology of Human Colorectal Cancer and Liver Metastases after Oxaliplatin-Based Chemotherapy
title_sort commitment of scaffold proteins in the onco-biology of human colorectal cancer and liver metastases after oxaliplatin-based chemotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412470/
https://www.ncbi.nlm.nih.gov/pubmed/28441737
http://dx.doi.org/10.3390/ijms18040891
work_keys_str_mv AT rotolideborah commitmentofscaffoldproteinsintheoncobiologyofhumancolorectalcancerandlivermetastasesafteroxaliplatinbasedchemotherapy
AT moralesmanuel commitmentofscaffoldproteinsintheoncobiologyofhumancolorectalcancerandlivermetastasesafteroxaliplatinbasedchemotherapy
AT avilajulio commitmentofscaffoldproteinsintheoncobiologyofhumancolorectalcancerandlivermetastasesafteroxaliplatinbasedchemotherapy
AT maesomariadelcarmen commitmentofscaffoldproteinsintheoncobiologyofhumancolorectalcancerandlivermetastasesafteroxaliplatinbasedchemotherapy
AT garciamariadelpino commitmentofscaffoldproteinsintheoncobiologyofhumancolorectalcancerandlivermetastasesafteroxaliplatinbasedchemotherapy
AT mobasheriali commitmentofscaffoldproteinsintheoncobiologyofhumancolorectalcancerandlivermetastasesafteroxaliplatinbasedchemotherapy
AT martinvasallopablo commitmentofscaffoldproteinsintheoncobiologyofhumancolorectalcancerandlivermetastasesafteroxaliplatinbasedchemotherapy