MAHDAL, Michal, Jakub NERADIL, Peter MÚDRY, Silvia PAUKOVČEKOVÁ, Iva ZAMBO, Jiří URBAN, Peter MACSEK, Lukáš PAZOUREK, Tomáš TOMÁŠ and Renata VESELSKÁ. 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. Cancers. Basel: MDPI, vol. 13, No 14, p. 3543-3557. ISSN 2072-6694. doi:10.3390/cancers13143543. 2021.
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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
Original language English
Type of outcome Article in a journal
Field of Study 30204 Oncology
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 6.575
RIV identification code RIV/00216224:14310/21:00120142
Organization unit Faculty of Science
Doi http://dx.doi.org/10.3390/cancers13143543
UT WoS 000677361200001
Keywords in English giant-cell tumor of bone; targeted treatment; sunitinib; PDGFR beta; denosumab; signaling
Tags 14110112, 14110123, 14110321, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 16/11/2021 15:48.
Abstract
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 MUName: Zkoumání účinku denosumabu na obrovskobuněčný kostní nádor v laboratorních podmínkách
Investor: Masaryk University, Category A
NV16-34083A, research and development projectName: Receptorové tyrozinkinázy a navazující signální dráhy jako potenciální cíle léčby refrakterních solidních nádorů dětského věku
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