Detailed Information on Publication Record
2021
New Target for Precision Medicine Treatment of Giant-Cell Tumor of Bone: Sunitinib Is Effective in the Treatment of Neoplastic Stromal Cells with Activated PDGFRβ Signaling
MAHDAL, Michal, Jakub NERADIL, Peter MÚDRY, Silvia PAUKOVČEKOVÁ, Iva ZAMBO et. al.Basic information
Original name
New Target for Precision Medicine Treatment of Giant-Cell Tumor of Bone: Sunitinib Is Effective in the Treatment of Neoplastic Stromal Cells with Activated PDGFRβ Signaling
Authors
MAHDAL, Michal (203 Czech Republic, belonging to the institution), Jakub NERADIL (203 Czech Republic, belonging to the institution), Peter MÚDRY (203 Czech Republic, belonging to the institution), Silvia PAUKOVČEKOVÁ (703 Slovakia, belonging to the institution), Iva ZAMBO (203 Czech Republic, belonging to the institution), Jiří URBAN (203 Czech Republic, belonging to the institution), Peter MACSEK (703 Slovakia, belonging to the institution), Lukáš PAZOUREK (203 Czech Republic, belonging to the institution), Tomáš TOMÁŠ (203 Czech Republic, belonging to the institution) and Renata VESELSKÁ (203 Czech Republic, guarantor, belonging to the institution)
Edition
Cancers, Basel, MDPI, 2021, 2072-6694
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30204 Oncology
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.575
RIV identification code
RIV/00216224:14310/21:00120142
Organization unit
Faculty of Science
UT WoS
000677361200001
Keywords in English
giant-cell tumor of bone; targeted treatment; sunitinib; PDGFR beta; denosumab; signaling
Tags
International impact, Reviewed
Změněno: 16/11/2021 15:48, Mgr. Marie Šípková, DiS.
Abstract
V originále
The purpose of this study was to analyze differential cell signaling in response to denosumab treatment to identify and subsequently inhibit molecular targets in the neoplastic stromal cell population, which poses a risk for tumor recurrence. Using phosphoprotein arrays, a distinct signaling profile was detected in GCTB tissues treated with denosumab, a specific RANKL antibody, which coincided with the RTK profile in derived cell lines. PDGFRβ was selected as a promising receptor target, and its inhibition by the small-molecule inhibitor sunitinib resulted in potent inhibition of cell proliferation in vitro. The addition of sunitinib to denosumab resulted in the disappearance of both multinuclear giant cells and neoplastic stromal cells, as reported here. Thus, sunitinib could become an effective addition to denosumab in the treatment of GCTB with activated PDGFRβ.
Links
MUNI/A/1477/2018, interní kód MU |
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NV16-34083A, research and development project |
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