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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-...
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Published in: | Cancers 2023-11, Vol.15 (22), p.5422 |
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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 |
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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/). 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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. 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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> |
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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 |
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