Cargando…

Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity

Relapse after chemotherapy treatment depends on the cancer initiating cells (CICs). PEDF (Pigmented Epithelium Derived Factor) is an anti-angiogenic, neurotrophic and self-renewal regulator molecule, also involved in CICs biology. Acute and chronic exposition of colon cancer cell lines to CT/CTE PED...

Descripción completa

Detalles Bibliográficos
Autores principales: Honrubia-Gómez, Paloma, López-Garrido, María-Pilar, Gil-Gas, Carmen, Sánchez-Sánchez, José, Alvarez-Simon, Carmen, Cuenca-Escalona, Jorge, Perez, Ana Ferrer, Arias, Enrique, Moreno, Raul, Sánchez-Sánchez, Francisco, Ramirez-Castillejo, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508205/
https://www.ncbi.nlm.nih.gov/pubmed/31105879
http://dx.doi.org/10.18632/oncotarget.26085
_version_ 1783417079113711616
author Honrubia-Gómez, Paloma
López-Garrido, María-Pilar
Gil-Gas, Carmen
Sánchez-Sánchez, José
Alvarez-Simon, Carmen
Cuenca-Escalona, Jorge
Perez, Ana Ferrer
Arias, Enrique
Moreno, Raul
Sánchez-Sánchez, Francisco
Ramirez-Castillejo, Carmen
author_facet Honrubia-Gómez, Paloma
López-Garrido, María-Pilar
Gil-Gas, Carmen
Sánchez-Sánchez, José
Alvarez-Simon, Carmen
Cuenca-Escalona, Jorge
Perez, Ana Ferrer
Arias, Enrique
Moreno, Raul
Sánchez-Sánchez, Francisco
Ramirez-Castillejo, Carmen
author_sort Honrubia-Gómez, Paloma
collection PubMed
description Relapse after chemotherapy treatment depends on the cancer initiating cells (CICs). PEDF (Pigmented Epithelium Derived Factor) is an anti-angiogenic, neurotrophic and self-renewal regulator molecule, also involved in CICs biology. Acute and chronic exposition of colon cancer cell lines to CT/CTE PEDF-derived peptides decreased drug-resistance to conventional colorectal cancer treatments, such as oxaliplatin or irinotecan. We confirmed a reduction in the irinotecan and oxaliplatin IC50 doses for all tested tumour cell lines. After xenograft transplantation, CT/CTE treatments also produced a reduction in resistance to conventional chemotherapy treatments as in culture-assays. Metastatic capacity of these treated cell lines was also depleted. The PEDF signaling pathway could be a future therapeutic tool for use as an adjuvant therapy that decreases IC50 dosis, adverse effects and treatment costs. This pathway could also be involved in an increase of the time relapse in patients, decreased tumourigenicity, and decreased capacity to produce metastasis.
format Online
Article
Text
id pubmed-6508205
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-65082052019-05-17 Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity Honrubia-Gómez, Paloma López-Garrido, María-Pilar Gil-Gas, Carmen Sánchez-Sánchez, José Alvarez-Simon, Carmen Cuenca-Escalona, Jorge Perez, Ana Ferrer Arias, Enrique Moreno, Raul Sánchez-Sánchez, Francisco Ramirez-Castillejo, Carmen Oncotarget Research Paper Relapse after chemotherapy treatment depends on the cancer initiating cells (CICs). PEDF (Pigmented Epithelium Derived Factor) is an anti-angiogenic, neurotrophic and self-renewal regulator molecule, also involved in CICs biology. Acute and chronic exposition of colon cancer cell lines to CT/CTE PEDF-derived peptides decreased drug-resistance to conventional colorectal cancer treatments, such as oxaliplatin or irinotecan. We confirmed a reduction in the irinotecan and oxaliplatin IC50 doses for all tested tumour cell lines. After xenograft transplantation, CT/CTE treatments also produced a reduction in resistance to conventional chemotherapy treatments as in culture-assays. Metastatic capacity of these treated cell lines was also depleted. The PEDF signaling pathway could be a future therapeutic tool for use as an adjuvant therapy that decreases IC50 dosis, adverse effects and treatment costs. This pathway could also be involved in an increase of the time relapse in patients, decreased tumourigenicity, and decreased capacity to produce metastasis. Impact Journals LLC 2019-04-26 /pmc/articles/PMC6508205/ /pubmed/31105879 http://dx.doi.org/10.18632/oncotarget.26085 Text en Copyright: © 2019 Honrubia-Gómez et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Honrubia-Gómez, Paloma
López-Garrido, María-Pilar
Gil-Gas, Carmen
Sánchez-Sánchez, José
Alvarez-Simon, Carmen
Cuenca-Escalona, Jorge
Perez, Ana Ferrer
Arias, Enrique
Moreno, Raul
Sánchez-Sánchez, Francisco
Ramirez-Castillejo, Carmen
Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity
title Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity
title_full Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity
title_fullStr Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity
title_full_unstemmed Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity
title_short Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity
title_sort pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508205/
https://www.ncbi.nlm.nih.gov/pubmed/31105879
http://dx.doi.org/10.18632/oncotarget.26085
work_keys_str_mv AT honrubiagomezpaloma pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT lopezgarridomariapilar pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT gilgascarmen pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT sanchezsanchezjose pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT alvarezsimoncarmen pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT cuencaescalonajorge pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT perezanaferrer pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT ariasenrique pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT morenoraul pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT sanchezsanchezfrancisco pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity
AT ramirezcastillejocarmen pedfderivedpeptidesaffectcolorectalcancercelllinesresistanceandtumourregrowthcapacity