Loading…

Self-Renewal Inhibition in Breast Cancer Stem Cells: Moonlight Role of PEDF in Breast Cancer

Breast cancer is the leading cause of death among females in developed countries. Although the implementation of screening tests and the development of new therapies have increased the probability of remission, relapse rates remain high. Numerous studies have indicated the connection between cancer-...

Full description

Saved in:
Bibliographic Details
Published in:Cancers 2023-11, Vol.15 (22), p.5422
Main Authors: Gil-Gas, Carmen, Sánchez-Díez, Marta, Honrubia-Gómez, Paloma, Sánchez-Sánchez, Jose Luis, Alvarez-Simón, Carmen B, Sabater, Sebastia, Sánchez-Sánchez, Francisco, Ramírez-Castillejo, Carmen
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c364t-fc78138890b32f32a2771777910b34a8071660a5a0128d5b881341a2def39883
container_end_page
container_issue 22
container_start_page 5422
container_title Cancers
container_volume 15
creator Gil-Gas, Carmen
Sánchez-Díez, Marta
Honrubia-Gómez, Paloma
Sánchez-Sánchez, Jose Luis
Alvarez-Simón, Carmen B
Sabater, Sebastia
Sánchez-Sánchez, Francisco
Ramírez-Castillejo, Carmen
description Breast cancer is the leading cause of death among females in developed countries. Although the implementation of screening tests and the development of new therapies have increased the probability of remission, relapse rates remain high. Numerous studies have indicated the connection between cancer-initiating cells and slow cellular cycle cells, identified by their capacity to retain long labeling (LT+). In this study, we perform new assays showing how stem cell self-renewal modulating proteins, such as PEDF, can modify the properties, percentage of biomarker-expressing cells, and carcinogenicity of cancer stem cells. The PEDF signaling pathway could be a useful tool for controlling cancer stem cells’ self-renewal and therefore control patient relapse, as PEDF enhances resistance in breast cancer patient cells’ in vitro culture. We have designed a peptide consisting of the C-terminal part of this protein, which acts by blocking endogenous PEDF in cell culture assays. We demonstrate that it is possible to interfere with the self-renewal capacity of cancer stem cells, induce anoikis in vivo, and reduce resistance against docetaxel treatment in cancer patient cells in in vitro culture. We have also demonstrated that this modified PEDF protein produces a significant decrease in the percentage of expressed cancer stem cell markers.
doi_str_mv 10.3390/cancers15225422
format article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2893845475</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A774318469</galeid><sourcerecordid>A774318469</sourcerecordid><originalsourceid>FETCH-LOGICAL-c364t-fc78138890b32f32a2771777910b34a8071660a5a0128d5b881341a2def39883</originalsourceid><addsrcrecordid>eNptkc1LAzEQxRdRsNSevQa8eFmbr91kvdW11UJFaXsUlnSbtClpUpMt4n9v2gpqdeYww_B7jweTJJcI3hBSwG4tbC19QBnGGcX4JGlhyHCa5wU9_bGfJ50QVjAWIYjlrJW8TqRR6Vha-S4MGNqlnulGOwu0BXdeitCAcu8NJo1cg1IaE27Bk3PW6MWyAWNnJHAKvPTvB380F8mZEibIztdsJ9NBf1o-pqPnh2HZG6U1yWmTqppxRDgv4IxgRbDAjCHGWIHigQoOGcpzKDIBEebzbMYjTZHAc6lIwTlpJ9cH2413b1sZmmqtQx2TCivdNlSYF4TTjLIsoldH6MptvY3h9hQkecHIN7UQRlbaKtd4Ue9Mqx5jlCBO8yJSN_9QsedyrWtnpdLx_kvQPQhq70LwUlUbr9fCf1QIVrs3VkdvJJ--TYv_</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2893036973</pqid></control><display><type>article</type><title>Self-Renewal Inhibition in Breast Cancer Stem Cells: Moonlight Role of PEDF in Breast Cancer</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central</source><creator>Gil-Gas, Carmen ; Sánchez-Díez, Marta ; Honrubia-Gómez, Paloma ; Sánchez-Sánchez, Jose Luis ; Alvarez-Simón, Carmen B ; Sabater, Sebastia ; Sánchez-Sánchez, Francisco ; Ramírez-Castillejo, Carmen</creator><creatorcontrib>Gil-Gas, Carmen ; Sánchez-Díez, Marta ; Honrubia-Gómez, Paloma ; Sánchez-Sánchez, Jose Luis ; Alvarez-Simón, Carmen B ; Sabater, Sebastia ; Sánchez-Sánchez, Francisco ; Ramírez-Castillejo, Carmen</creatorcontrib><description>Breast cancer is the leading cause of death among females in developed countries. Although the implementation of screening tests and the development of new therapies have increased the probability of remission, relapse rates remain high. Numerous studies have indicated the connection between cancer-initiating cells and slow cellular cycle cells, identified by their capacity to retain long labeling (LT+). In this study, we perform new assays showing how stem cell self-renewal modulating proteins, such as PEDF, can modify the properties, percentage of biomarker-expressing cells, and carcinogenicity of cancer stem cells. The PEDF signaling pathway could be a useful tool for controlling cancer stem cells’ self-renewal and therefore control patient relapse, as PEDF enhances resistance in breast cancer patient cells’ in vitro culture. We have designed a peptide consisting of the C-terminal part of this protein, which acts by blocking endogenous PEDF in cell culture assays. We demonstrate that it is possible to interfere with the self-renewal capacity of cancer stem cells, induce anoikis in vivo, and reduce resistance against docetaxel treatment in cancer patient cells in in vitro culture. We have also demonstrated that this modified PEDF protein produces a significant decrease in the percentage of expressed cancer stem cell markers.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15225422</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Amino acids ; Anoikis ; Apoptosis ; Biomarkers ; Breast cancer ; Cancer ; Cancer therapies ; Carcinogenicity ; Cell culture ; Cell self-renewal ; Chemotherapy ; Development and progression ; Glycoproteins ; Metastases ; Metastasis ; Oncology, Experimental ; Patients ; Peptides ; Phosphorylation ; Prevention ; Proteins ; Quality of life ; Remission ; Signal transduction ; Stem cells ; Tumor cells ; Tumors</subject><ispartof>Cancers, 2023-11, Vol.15 (22), p.5422</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 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 (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c364t-fc78138890b32f32a2771777910b34a8071660a5a0128d5b881341a2def39883</cites><orcidid>0000-0002-1877-3381</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2893036973/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2893036973?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590,75126</link.rule.ids></links><search><creatorcontrib>Gil-Gas, Carmen</creatorcontrib><creatorcontrib>Sánchez-Díez, Marta</creatorcontrib><creatorcontrib>Honrubia-Gómez, Paloma</creatorcontrib><creatorcontrib>Sánchez-Sánchez, Jose Luis</creatorcontrib><creatorcontrib>Alvarez-Simón, Carmen B</creatorcontrib><creatorcontrib>Sabater, Sebastia</creatorcontrib><creatorcontrib>Sánchez-Sánchez, Francisco</creatorcontrib><creatorcontrib>Ramírez-Castillejo, Carmen</creatorcontrib><title>Self-Renewal Inhibition in Breast Cancer Stem Cells: Moonlight Role of PEDF in Breast Cancer</title><title>Cancers</title><description>Breast cancer is the leading cause of death among females in developed countries. Although the implementation of screening tests and the development of new therapies have increased the probability of remission, relapse rates remain high. Numerous studies have indicated the connection between cancer-initiating cells and slow cellular cycle cells, identified by their capacity to retain long labeling (LT+). In this study, we perform new assays showing how stem cell self-renewal modulating proteins, such as PEDF, can modify the properties, percentage of biomarker-expressing cells, and carcinogenicity of cancer stem cells. The PEDF signaling pathway could be a useful tool for controlling cancer stem cells’ self-renewal and therefore control patient relapse, as PEDF enhances resistance in breast cancer patient cells’ in vitro culture. We have designed a peptide consisting of the C-terminal part of this protein, which acts by blocking endogenous PEDF in cell culture assays. We demonstrate that it is possible to interfere with the self-renewal capacity of cancer stem cells, induce anoikis in vivo, and reduce resistance against docetaxel treatment in cancer patient cells in in vitro culture. We have also demonstrated that this modified PEDF protein produces a significant decrease in the percentage of expressed cancer stem cell markers.</description><subject>Amino acids</subject><subject>Anoikis</subject><subject>Apoptosis</subject><subject>Biomarkers</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Carcinogenicity</subject><subject>Cell culture</subject><subject>Cell self-renewal</subject><subject>Chemotherapy</subject><subject>Development and progression</subject><subject>Glycoproteins</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Oncology, Experimental</subject><subject>Patients</subject><subject>Peptides</subject><subject>Phosphorylation</subject><subject>Prevention</subject><subject>Proteins</subject><subject>Quality of life</subject><subject>Remission</subject><subject>Signal transduction</subject><subject>Stem cells</subject><subject>Tumor cells</subject><subject>Tumors</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkc1LAzEQxRdRsNSevQa8eFmbr91kvdW11UJFaXsUlnSbtClpUpMt4n9v2gpqdeYww_B7jweTJJcI3hBSwG4tbC19QBnGGcX4JGlhyHCa5wU9_bGfJ50QVjAWIYjlrJW8TqRR6Vha-S4MGNqlnulGOwu0BXdeitCAcu8NJo1cg1IaE27Bk3PW6MWyAWNnJHAKvPTvB380F8mZEibIztdsJ9NBf1o-pqPnh2HZG6U1yWmTqppxRDgv4IxgRbDAjCHGWIHigQoOGcpzKDIBEebzbMYjTZHAc6lIwTlpJ9cH2413b1sZmmqtQx2TCivdNlSYF4TTjLIsoldH6MptvY3h9hQkecHIN7UQRlbaKtd4Ue9Mqx5jlCBO8yJSN_9QsedyrWtnpdLx_kvQPQhq70LwUlUbr9fCf1QIVrs3VkdvJJ--TYv_</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Gil-Gas, Carmen</creator><creator>Sánchez-Díez, Marta</creator><creator>Honrubia-Gómez, Paloma</creator><creator>Sánchez-Sánchez, Jose Luis</creator><creator>Alvarez-Simón, Carmen B</creator><creator>Sabater, Sebastia</creator><creator>Sánchez-Sánchez, Francisco</creator><creator>Ramírez-Castillejo, Carmen</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1877-3381</orcidid></search><sort><creationdate>20231101</creationdate><title>Self-Renewal Inhibition in Breast Cancer Stem Cells: Moonlight Role of PEDF in Breast Cancer</title><author>Gil-Gas, Carmen ; Sánchez-Díez, Marta ; Honrubia-Gómez, Paloma ; Sánchez-Sánchez, Jose Luis ; Alvarez-Simón, Carmen B ; Sabater, Sebastia ; Sánchez-Sánchez, Francisco ; Ramírez-Castillejo, Carmen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c364t-fc78138890b32f32a2771777910b34a8071660a5a0128d5b881341a2def39883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino acids</topic><topic>Anoikis</topic><topic>Apoptosis</topic><topic>Biomarkers</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Carcinogenicity</topic><topic>Cell culture</topic><topic>Cell self-renewal</topic><topic>Chemotherapy</topic><topic>Development and progression</topic><topic>Glycoproteins</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Oncology, Experimental</topic><topic>Patients</topic><topic>Peptides</topic><topic>Phosphorylation</topic><topic>Prevention</topic><topic>Proteins</topic><topic>Quality of life</topic><topic>Remission</topic><topic>Signal transduction</topic><topic>Stem cells</topic><topic>Tumor cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gil-Gas, Carmen</creatorcontrib><creatorcontrib>Sánchez-Díez, Marta</creatorcontrib><creatorcontrib>Honrubia-Gómez, Paloma</creatorcontrib><creatorcontrib>Sánchez-Sánchez, Jose Luis</creatorcontrib><creatorcontrib>Alvarez-Simón, Carmen B</creatorcontrib><creatorcontrib>Sabater, Sebastia</creatorcontrib><creatorcontrib>Sánchez-Sánchez, Francisco</creatorcontrib><creatorcontrib>Ramírez-Castillejo, Carmen</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest research library</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gil-Gas, Carmen</au><au>Sánchez-Díez, Marta</au><au>Honrubia-Gómez, Paloma</au><au>Sánchez-Sánchez, Jose Luis</au><au>Alvarez-Simón, Carmen B</au><au>Sabater, Sebastia</au><au>Sánchez-Sánchez, Francisco</au><au>Ramírez-Castillejo, Carmen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Self-Renewal Inhibition in Breast Cancer Stem Cells: Moonlight Role of PEDF in Breast Cancer</atitle><jtitle>Cancers</jtitle><date>2023-11-01</date><risdate>2023</risdate><volume>15</volume><issue>22</issue><spage>5422</spage><pages>5422-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Breast cancer is the leading cause of death among females in developed countries. Although the implementation of screening tests and the development of new therapies have increased the probability of remission, relapse rates remain high. Numerous studies have indicated the connection between cancer-initiating cells and slow cellular cycle cells, identified by their capacity to retain long labeling (LT+). In this study, we perform new assays showing how stem cell self-renewal modulating proteins, such as PEDF, can modify the properties, percentage of biomarker-expressing cells, and carcinogenicity of cancer stem cells. The PEDF signaling pathway could be a useful tool for controlling cancer stem cells’ self-renewal and therefore control patient relapse, as PEDF enhances resistance in breast cancer patient cells’ in vitro culture. We have designed a peptide consisting of the C-terminal part of this protein, which acts by blocking endogenous PEDF in cell culture assays. We demonstrate that it is possible to interfere with the self-renewal capacity of cancer stem cells, induce anoikis in vivo, and reduce resistance against docetaxel treatment in cancer patient cells in in vitro culture. We have also demonstrated that this modified PEDF protein produces a significant decrease in the percentage of expressed cancer stem cell markers.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/cancers15225422</doi><orcidid>https://orcid.org/0000-0002-1877-3381</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2072-6694
ispartof Cancers, 2023-11, Vol.15 (22), p.5422
issn 2072-6694
2072-6694
language eng
recordid cdi_proquest_miscellaneous_2893845475
source Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central
subjects Amino acids
Anoikis
Apoptosis
Biomarkers
Breast cancer
Cancer
Cancer therapies
Carcinogenicity
Cell culture
Cell self-renewal
Chemotherapy
Development and progression
Glycoproteins
Metastases
Metastasis
Oncology, Experimental
Patients
Peptides
Phosphorylation
Prevention
Proteins
Quality of life
Remission
Signal transduction
Stem cells
Tumor cells
Tumors
title Self-Renewal Inhibition in Breast Cancer Stem Cells: Moonlight Role of PEDF in Breast Cancer
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T22%3A51%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Self-Renewal%20Inhibition%20in%20Breast%20Cancer%20Stem%20Cells:%20Moonlight%20Role%20of%20PEDF%20in%20Breast%20Cancer&rft.jtitle=Cancers&rft.au=Gil-Gas,%20Carmen&rft.date=2023-11-01&rft.volume=15&rft.issue=22&rft.spage=5422&rft.pages=5422-&rft.issn=2072-6694&rft.eissn=2072-6694&rft_id=info:doi/10.3390/cancers15225422&rft_dat=%3Cgale_proqu%3EA774318469%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c364t-fc78138890b32f32a2771777910b34a8071660a5a0128d5b881341a2def39883%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2893036973&rft_id=info:pmid/&rft_galeid=A774318469&rfr_iscdi=true