Breast cancer genes PSMC3IP and EPSTI1 play a role in apoptosis regulation.

A key element to delineate the biology of individual tumors is the regulation of apoptosis. In this work, we functionally characterize two breast cancer associated genes, the proteasome 26S subunit ATPase 3 interacting protein (PSMC3IP) and the epithelial-stromal interaction 1 (EPSTI1), to explore t...

Full description

Bibliographic Details
Main Authors: Eva Capdevila-Busquets, Nahuai Badiola, Rodrigo Arroyo, Víctor Alcalde, Montserrat Soler-López, Patrick Aloy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4295872?pdf=render
id doaj-31564e56bef549a9a535730a3082960c
record_format Article
spelling doaj-31564e56bef549a9a535730a3082960c2020-11-25T01:56:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01101e011535210.1371/journal.pone.0115352Breast cancer genes PSMC3IP and EPSTI1 play a role in apoptosis regulation.Eva Capdevila-BusquetsNahuai BadiolaRodrigo ArroyoVíctor AlcaldeMontserrat Soler-LópezPatrick AloyA key element to delineate the biology of individual tumors is the regulation of apoptosis. In this work, we functionally characterize two breast cancer associated genes, the proteasome 26S subunit ATPase 3 interacting protein (PSMC3IP) and the epithelial-stromal interaction 1 (EPSTI1), to explore their potential apoptotic role in breast cancer. We first explore the existence of direct physical interactions with annotated BC-apoptotic genes. Based on the generated interaction network, we examine several apoptotic markers to determine the effect of PSMC3IP and EPSTI1 gene expression modulation in two different human breast cancer cell lines to suggest potential molecular mechanisms to unveil their role in the disease. Our results show that PSMC3IP and EPSTI1 are able to modulate the extrinsic apoptotic pathway in estrogen receptor positive and triple negative breast cancer cell lines, highlighting them as potential therapeutic targets.http://europepmc.org/articles/PMC4295872?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Eva Capdevila-Busquets
Nahuai Badiola
Rodrigo Arroyo
Víctor Alcalde
Montserrat Soler-López
Patrick Aloy
spellingShingle Eva Capdevila-Busquets
Nahuai Badiola
Rodrigo Arroyo
Víctor Alcalde
Montserrat Soler-López
Patrick Aloy
Breast cancer genes PSMC3IP and EPSTI1 play a role in apoptosis regulation.
PLoS ONE
author_facet Eva Capdevila-Busquets
Nahuai Badiola
Rodrigo Arroyo
Víctor Alcalde
Montserrat Soler-López
Patrick Aloy
author_sort Eva Capdevila-Busquets
title Breast cancer genes PSMC3IP and EPSTI1 play a role in apoptosis regulation.
title_short Breast cancer genes PSMC3IP and EPSTI1 play a role in apoptosis regulation.
title_full Breast cancer genes PSMC3IP and EPSTI1 play a role in apoptosis regulation.
title_fullStr Breast cancer genes PSMC3IP and EPSTI1 play a role in apoptosis regulation.
title_full_unstemmed Breast cancer genes PSMC3IP and EPSTI1 play a role in apoptosis regulation.
title_sort breast cancer genes psmc3ip and epsti1 play a role in apoptosis regulation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description A key element to delineate the biology of individual tumors is the regulation of apoptosis. In this work, we functionally characterize two breast cancer associated genes, the proteasome 26S subunit ATPase 3 interacting protein (PSMC3IP) and the epithelial-stromal interaction 1 (EPSTI1), to explore their potential apoptotic role in breast cancer. We first explore the existence of direct physical interactions with annotated BC-apoptotic genes. Based on the generated interaction network, we examine several apoptotic markers to determine the effect of PSMC3IP and EPSTI1 gene expression modulation in two different human breast cancer cell lines to suggest potential molecular mechanisms to unveil their role in the disease. Our results show that PSMC3IP and EPSTI1 are able to modulate the extrinsic apoptotic pathway in estrogen receptor positive and triple negative breast cancer cell lines, highlighting them as potential therapeutic targets.
url http://europepmc.org/articles/PMC4295872?pdf=render
work_keys_str_mv AT evacapdevilabusquets breastcancergenespsmc3ipandepsti1playaroleinapoptosisregulation
AT nahuaibadiola breastcancergenespsmc3ipandepsti1playaroleinapoptosisregulation
AT rodrigoarroyo breastcancergenespsmc3ipandepsti1playaroleinapoptosisregulation
AT victoralcalde breastcancergenespsmc3ipandepsti1playaroleinapoptosisregulation
AT montserratsolerlopez breastcancergenespsmc3ipandepsti1playaroleinapoptosisregulation
AT patrickaloy breastcancergenespsmc3ipandepsti1playaroleinapoptosisregulation
_version_ 1724977472391348224