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Cadherin-6 is a novel mediator for the migration of mesenchymal stem cells to glioblastoma cells in response to stromal cell-derived factor-1

Authors
 Aran Park  ;  Seung-Eun Kim  ;  Jinyeong Yu  ;  Donghyun Son  ;  Kyung-Sup Kim  ;  Eunjin Koh  ;  Ki-Sook Park 
Citation
 FEBS OPEN BIO, Vol.14(7) : 1192-1204, 2024-07 
Journal Title
FEBS OPEN BIO
ISSN
 2211-5463 
Issue Date
2024-07
MeSH
Cadherins* / genetics ; Cadherins* / metabolism ; Cell Line, Tumor ; Cell Movement* / genetics ; Cell Proliferation / genetics ; Chemokine CXCL12* / metabolism ; Glioblastoma* / genetics ; Glioblastoma* / metabolism ; Glioblastoma* / pathology ; Humans ; Mesenchymal Stem Cells* / metabolism ; Tumor Microenvironment
Keywords
bone marrow‐derived mesenchymal stem cells ; cadherin‐6 ; glioblastoma ; migration ; stromal cell‐derived factor‐1
Abstract
Glioblastoma recruits various nontransformed cells from distant tissues. Although bone marrow-derived mesenchymal stem cells (MSCs) have been observed migrating to glioblastoma, the underlying mechanism driving MSC migration toward glioblastoma remains unclear. Tumor vascularity is critical in the context of recurrent glioblastoma and is closely linked to the expression of stromal cell-derived factor-1 (SDF-1). We demonstrated that cadherin-6 mediated MSC migration both toward SDF-1 and toward glioblastoma cells. Cadherin-6 knockdown resulted in the downregulation of MSCs capacity to migrate in response to SDF-1. Furthermore, MSCs with cadherin-6 knockdown exhibited impaired migration in response to conditioned media derived from glioblastoma cell lines (U87 and U373) expressing SDF-1, thus simulating the glioblastoma microenvironment. Moreover, MSCs enhanced the vasculogenic capacity of U87 cells without increasing the proliferation, cancer stem cell characteristics, or migration of U87. These results suggest that the current strategy of utilizing MSCs as carriers for antiglioblastoma drugs requires careful examination. Furthermore, cadherin-6 may represent a novel potential target for controlling the recruitment of MSCs toward glioblastoma.
Files in This Item:
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DOI
10.1002/2211-5463.13815
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biochemistry and Molecular Biology (생화학-분자생물학교실) > 1. Journal Papers
Yonsei Authors
Koh, Eun Jin(고은진) ORCID logo https://orcid.org/0000-0001-8967-6266
Kim, Kyung Sup(김경섭) ORCID logo https://orcid.org/0000-0001-8483-8537
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/204263
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