Identification of novel therapeutic targets in the secretome of ionizing radiation-induced senescent tumor cells
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hwang, Hyun Jung | - |
dc.contributor.author | Jung, Seung Hee | - |
dc.contributor.author | Lee, Hyung Chul | - |
dc.contributor.author | Han, Na Kyung | - |
dc.contributor.author | Bae, In Hwa | - |
dc.contributor.author | Lee, Minyoung | - |
dc.contributor.author | Han, Young-Hoon | - |
dc.contributor.author | Kang, Young-Sun | - |
dc.contributor.author | Lee, Su-Jae | - |
dc.contributor.author | Park, Heon Joo | - |
dc.contributor.author | Ko, Young-Gyu | - |
dc.contributor.author | Lee, Jae-Seon | - |
dc.date.accessioned | 2021-09-04T03:18:37Z | - |
dc.date.available | 2021-09-04T03:18:37Z | - |
dc.date.created | 2021-06-18 | - |
dc.date.issued | 2016-02 | - |
dc.identifier.issn | 1021-335X | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/89584 | - |
dc.description.abstract | Cellular senescence is a state of irreversible growth arrest that can be triggered by multiple mechanisms, including telomere shortening, the epigenetic derepression of the INK4 alpha/ARF locus and DNA damage. Senescence has been considered a tumor-suppressing mechanism that permanently arrests cells at risk for malignant transformation. However, accumulating evidence shows that senescent cells have deleterious effects on the tissue microenvironment. Some of these effects could be attributed to the senescence-associated secretory phenotype that has the ability to promote tumor progression. However, secreted proteins from senescent tumor cells and their effects on the tumor microenvironment due to ionizing radiation (IR) exposure have not yet been fully elucidated. In the present study, we analyzed cytokines secreted from IR-induced senescent MCF7 cells by using cytokine microarrays and confirmed by western blot analysis that increased secretion of osteoprotegerin (OPG), midkine (MDK) and apolipoprotein E3 (ApoE3) occurs in these cells. Invasive, migratory and wound-healing activities were observed in MDA-MB-231 and MCF-10A cells following treatment with recombinant human OPG, MDK and ApoE3 proteins. Additionally, tube-formation activity was assessed in OPG-, MDK- and ApoE3-treated human umbilical vein endothelial cells (HUVECs). We found that OPG, MDK and ApoE3 affected cell motility and tube-formation activity. Since OPG markedly affected cell motility, we examined the effect of senescent conditioned media containing neutralizing OPG antibodies on migration and wound-healing activity. Our results demonstrated that IR-induced senescent tumor cells influence the tumor microenvironment by increasing the production of cytokines, such as OPG, MDK and ApoE3. Furthermore, these data suggest that OPG is likely a promising target capable of reducing the deleterious effects on the tumor microenvironment during radiation therapy. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | SPANDIDOS PUBL LTD | - |
dc.subject | CELLULAR SENESCENCE | - |
dc.subject | APOLIPOPROTEIN-E | - |
dc.subject | TELOMERE DYSFUNCTION | - |
dc.subject | CANCER DEVELOPMENT | - |
dc.subject | SELF-RENEWAL | - |
dc.subject | SUPPRESSION | - |
dc.subject | EXPRESSION | - |
dc.subject | MIDKINE | - |
dc.subject | SYSTEM | - |
dc.subject | PROLIFERATION | - |
dc.title | Identification of novel therapeutic targets in the secretome of ionizing radiation-induced senescent tumor cells | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Ko, Young-Gyu | - |
dc.identifier.doi | 10.3892/or.2015.4473 | - |
dc.identifier.scopusid | 2-s2.0-84954285664 | - |
dc.identifier.wosid | 000368049600028 | - |
dc.identifier.bibliographicCitation | ONCOLOGY REPORTS, v.35, no.2, pp.841 - 850 | - |
dc.relation.isPartOf | ONCOLOGY REPORTS | - |
dc.citation.title | ONCOLOGY REPORTS | - |
dc.citation.volume | 35 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 841 | - |
dc.citation.endPage | 850 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Oncology | - |
dc.relation.journalWebOfScienceCategory | Oncology | - |
dc.subject.keywordPlus | CELLULAR SENESCENCE | - |
dc.subject.keywordPlus | APOLIPOPROTEIN-E | - |
dc.subject.keywordPlus | TELOMERE DYSFUNCTION | - |
dc.subject.keywordPlus | CANCER DEVELOPMENT | - |
dc.subject.keywordPlus | SELF-RENEWAL | - |
dc.subject.keywordPlus | SUPPRESSION | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | MIDKINE | - |
dc.subject.keywordPlus | SYSTEM | - |
dc.subject.keywordPlus | PROLIFERATION | - |
dc.subject.keywordAuthor | cytokine | - |
dc.subject.keywordAuthor | radiation | - |
dc.subject.keywordAuthor | senescent cancer cells | - |
dc.subject.keywordAuthor | TNERSR11B | - |
dc.subject.keywordAuthor | invasion | - |
dc.subject.keywordAuthor | migration | - |
dc.subject.keywordAuthor | wound healing | - |
dc.subject.keywordAuthor | angiogenesis | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
(02841) 서울특별시 성북구 안암로 14502-3290-1114
COPYRIGHT © 2021 Korea University. All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.