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Naslov:CXCR4 antagonists as stem cell mobilizers and therapy sensitizers for acute myeloid leukemia and glioblastoma?
Avtorji:ID Hira, Vashendriya V. V. (Avtor)
ID Noorden, Cornelis J. F. van (Avtor)
ID Molenaar, Remco J. (Avtor)
Datoteke:URL URL - Izvorni URL, za dostop obiščite https://www.mdpi.com/2079-7737/9/2/31
 
.pdf PDF - Predstavitvena datoteka, prenos (1,51 MB)
MD5: 141860D0097387337E12B9B19A571323
 
URL URL - Izvorni URL, za dostop obiščite https://doi.org/10.3390/biology9020031
 
Jezik:Angleški jezik
Tipologija:1.03 - Drugi znanstveni članki
Organizacija:Logo NIB - Nacionalni inštitut za biologijo
Povzetek:Glioblastoma is the most aggressive and malignant primary brain tumor in adults and has a poor patient survival of only 20 months after diagnosis. This poor patient survival is at least partly caused by glioblastoma stem cells (GSCs), which are slowly-dividing and therefore therapy-resistant. GSCs are localized in protective hypoxic peri-arteriolar niches where these aforementioned stemness properties are maintained. We previously showed that hypoxic peri-arteriolar GSC niches in human glioblastoma are functionally similar to hypoxic peri-arteriolar hematopoietic stem cell (HSC) niches in human bone marrow. GSCs and HSCs express the receptor C-X-C receptor type 4 (CXCR4), which binds to the chemoattractant stromal-derived factor-1α (SDF-1α), which is highly expressed in GSC niches in glioblastoma and HSC niches in bone marrow. This receptor–ligand interaction retains the GSCs/HSCs in their niches and thereby maintains their slowly-dividing state. In acute myeloid leukemia (AML), leukemic cells use the SDF-1α–CXCR4 interaction to migrate to HSC niches and become slowly-dividing and therapy-resistant leukemic stem cells (LSCs). In this communication, we aim to elucidate how disruption of the SDF-1α–CXCR4 interaction using the FDA-approved CXCR4 inhibitor plerixafor (AMD3100) may be used to force slowly-dividing cancer stem cells out of their niches in glioblastoma and AML. Ultimately, this strategy aims to induce GSC and LSC differentiation and their sensitization to therapy.
Ključne besede:glioblastoma, glioblastoma stem cells, niches, acute myeloid leukemia, hematopoietic stem cells, bone marrow, C-X-C receptor type 4, stromal-derived factor-1 ▫$[alpha]$▫, plerixafor
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Datum objave:12.02.2020
Leto izida:2020
Št. strani:str. 1-10
Številčenje:Vol. 9, iss. 31
PID:20.500.12556/DiRROS-20163 Novo okno
UDK:577
ISSN pri članku:2079-7737
DOI:10.3390/biology9020031 Novo okno
COBISS.SI-ID:40521221 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 30. 3. 2020;
Datum objave v DiRROS:06.08.2024
Število ogledov:322
Število prenosov:406
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Biology
Skrajšan naslov:Biology
Založnik:MDPI AG
ISSN:2079-7737
COBISS.SI-ID:523004441 Novo okno

Gradivo je financirano iz projekta

Financer:Drugi - Drug financer ali več financerjev
Program financ.:the Dutch Cancer Society
Številka projekta:UVA 2014-6839

Financer:Drugi - Drug financer ali več financerjev
Program financ.:the Dutch Cancer Society
Številka projekta:UVA 2016.1-10460

Financer:Drugi - Drug financer ali več financerjev
Naslov:the Fondation pour la Recherche Nuovo-Soldati 2019

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:glioblastoma, matične celice, glioblastoma, akutna mielonična levkemija, kostni mozeg


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