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Overcoming sunitinib resistance with tocilizumab in renal cell carcinoma: Discordance between in vitro and in vivo effects.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2022 Jan 01; Vol. 586, pp. 42-48. Date of Electronic Publication: 2021 Nov 20. - Publication Year :
- 2022
-
Abstract
- Sunitinib is one of the first-line multi-tyrosine kinase inhibitors for metastatic renal cell carcinoma, and resistance to sunitinib continues to be a limiting factor for the successful treatment. As interleukin-6 (IL-6) is overexpressed in sunitinib-resistant cells, the purpose of this study was to explore the potential of IL-6 inhibition with tocilizumab, an IL-6 receptor inhibitor, to overcome resistance. In vitro, two sunitinib-resistant renal cell carcinoma cell lines (Caki-1 and SN12K1) were treated with tocilizumab. A mouse subcutaneous xenograft model was also used. Cell viability was studied by MTT assay, and apoptosis by morphology and ApopTag. Expression of IL-6, vascular endothelial growth factor (VEGF), and Bcl-2 was analyzed by qPCR. In vitro, tocilizumab induced significant cell death, and reduced the expression of IL-6, VEGF, and Bcl-2 in sunitinib-resistant cells. However, the in vitro findings could not be successfully translated in vivo, as tocilizumab did not decrease the growth of the tumors.<br />Competing Interests: Declaration of competing interest The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.<br /> (Copyright © 2021. Published by Elsevier Inc.)
- Subjects :
- Animals
Carcinoma, Renal Cell genetics
Carcinoma, Renal Cell metabolism
Carcinoma, Renal Cell pathology
Cell Line, Tumor
Cell Movement drug effects
Cell Proliferation drug effects
Cell Survival drug effects
Cell Survival genetics
Drug Resistance, Neoplasm genetics
Gene Expression Regulation, Neoplastic
Humans
Interleukin-6 genetics
Interleukin-6 metabolism
Kidney Neoplasms genetics
Kidney Neoplasms metabolism
Kidney Neoplasms pathology
Male
Mice, Nude
Neoplasm Metastasis
Proto-Oncogene Proteins c-bcl-2 genetics
Proto-Oncogene Proteins c-bcl-2 metabolism
Signal Transduction
Tumor Burden drug effects
Vascular Endothelial Growth Factor A genetics
Vascular Endothelial Growth Factor A metabolism
Xenograft Model Antitumor Assays
Mice
Antibodies, Monoclonal, Humanized pharmacology
Antineoplastic Agents pharmacology
Carcinoma, Renal Cell drug therapy
Drug Resistance, Neoplasm drug effects
Kidney Neoplasms drug therapy
Sunitinib pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 586
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 34826699
- Full Text :
- https://doi.org/10.1016/j.bbrc.2021.11.069