| Autor: |
Roberto Pili, Peter Hollenhorst, W. Andy Tao, Joseph Irudayaraj, Yong Zang, Paul R. Territo, Scott A. Persohn, Brian P. McCarthy, Heike Keilhack, Michael Buck, Janaiah Kota, Milan Radovich, Bradley Hancock, Mukund Seshadri, Giulio F. Draetta, Piergiorgio Pettazzoni, Sreevani Arisa, Eric Ciamporcero, May Elbanna, Li Shen, Kiersten Marie Miles, Ashley Orillion, Sreenivasulu Chintala, Chuan-Chih Hsu, Mary Ferris, Justine Arrington, Nur P. Damayanti, Justin Budka, Remi Adelaiye-Ogala |
| Rok vydání: |
2023 |
| Popis: |
Acquired and intrinsic resistance to receptor tyrosine kinase inhibitors (RTKi) represents a major hurdle in improving the management of clear cell renal cell carcinoma (ccRCC). Recent reports suggest that drug resistance is driven by tumor adaptation via epigenetic mechanisms that activate alternative survival pathways. The histone methyl transferase EZH2 is frequently altered in many cancers, including ccRCC. To evaluate its role in ccRCC resistance to RTKi, we established and characterized a spontaneously metastatic, patient-derived xenograft model that is intrinsically resistant to the RTKi sunitinib, but not to the VEGF therapeutic antibody bevacizumab. Sunitinib maintained its antiangiogenic and antimetastatic activity but lost its direct antitumor effects due to kinome reprogramming, which resulted in suppression of proapoptotic and cell-cycle–regulatory target genes. Modulating EZH2 expression or activity suppressed phosphorylation of certain RTKs, restoring the antitumor effects of sunitinib in models of acquired or intrinsically resistant ccRCC. Overall, our results highlight EZH2 as a rational target for therapeutic intervention in sunitinib-resistant ccRCC as well as a predictive marker for RTKi response in this disease. Cancer Res; 77(23); 6651–66. ©2017 AACR. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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