The combination of bevacizumab/Avastin and erlotinib/Tarceva is relevant for the treatment of metastatic renal cell carcinoma: the role of a synonymous mutation of the EGFR receptor
| Autor: | Hervé Quintens, Mélanie Guyot, Florence Dupré, Jérôme Durivault, Jean-François Roussel, Damien Ambrosetti, Gilles Pagès, Renaud Grépin, Aurore Dumond |
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| Rok vydání: | 2020 |
| Předmět: |
0301 basic medicine
Bevacizumab Cell Mice Nude Medicine (miscellaneous) Alpha interferon Antineoplastic Agents Erlotinib Hydrochloride Mice 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Germline mutation Cell Line Tumor medicine Animals Humans Epidermal growth factor receptor Carcinoma Renal Cell Pharmacology Toxicology and Pharmaceutics (miscellaneous) EGFR inhibitors biology business.industry Kidney Neoplasms Vascular endothelial growth factor HEK293 Cells 030104 developmental biology medicine.anatomical_structure chemistry 030220 oncology & carcinogenesis Cancer research biology.protein Drug Therapy Combination Female Erlotinib business Research Paper medicine.drug |
| Zdroj: | Theranostics |
| ISSN: | 1838-7640 |
| DOI: | 10.7150/thno.38346 |
| Popis: | Metastatic clear cell renal cell carcinomas (mRCC) over-express the vascular endothelial growth factor (VEGF). Hence, the anti-VEGF antibody bevacizumab/Avastin (BVZ) combined with interferon alpha (IFN) was approved for the treatment of mRCC. However, approval was lost in July 2016 due to the absence of sustained efficacy. We previously showed that BVZ accelerates tumor growth in experimental models of mRCC in mice, results in part explained by down-regulation of the phospho tyrosine phosphatase receptor kappa (PTPRκ) in tumor cells. The epidermal growth factor receptor (EGFR) is a direct target of PTPRκ. Its down-regulation leads to constitutive activation of EGFR, an observation which prompted us to test the effect of the EGFR inhibitor erlotinib/Tarceva (ERLO) in addition to BVZ/IFN. The influence of the long non-coding RNA, EGFR-AS1, on ERLO efficacy was also addressed. Methods: The effect of BVZ/IFN/ERLO was tested on the growth of experimental tumors in nude mice. The presence of germline mutation in the EGFR was evaluated on cell lines and primary RCC cells. In vitro translation and transfections of expression vectors coding the wild-type or the EGFR mutated gene in HEK-293 cells were used to test the role of EGFR mutation of the ERLO efficacy. Correlation between EGFR/EGFR-AS1 expression and survival was analyzed with an online available data base (TCGA). Results: Tumor growth was strongly reduced by the triple combination BVZ/IFN/ERLO and linked to reduced levels of pro-angiogenic/pro-inflammatory cytokines of the ELR+CXCL family and to subsequent inhibition of vascularization, a decreased number of lymphatic vessels and polarization of macrophages towards the M1 phenotype. Cells isolated from surgical resection of human tumors presented a range of sensitivity to ERLO depending on the presence of a newly detected mutation in the EGFR and to the presence of EGFR-AS1. Conclusions: Our results point-out that the BVZ/IFN/ERLO combination deserves testing for the treatment of mRCC that have a specific mutation in the EGFR. |
| Databáze: | OpenAIRE |
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