S. S. Emelianova, A. V. Volnitskiy, A. M. Solianik, N. H. Tran, L. A. Garaeva, R. A. Pantina, M. N. Grunina, E. D. Putevich, A. S. Potyseva, A. M. Golubev, V. S. Burdakov, N. A. Verlov, S. N. Naryzhnyy, A. L. Konevega, T. A. Shtam
{"title":"新胶质母细胞瘤细胞系:基因变化分析以及放疗和免疫疗法敏感性评估","authors":"S. S. Emelianova, A. V. Volnitskiy, A. M. Solianik, N. H. Tran, L. A. Garaeva, R. A. Pantina, M. N. Grunina, E. D. Putevich, A. S. Potyseva, A. M. Golubev, V. S. Burdakov, N. A. Verlov, S. N. Naryzhnyy, A. L. Konevega, T. A. Shtam","doi":"10.1134/S2635167624600871","DOIUrl":null,"url":null,"abstract":"<div><p>The characteristics of six new glioblastoma cell lines obtained from tumor material from patients are presented. The studied glioblastomas do not have mutations in the genes <i>IDH1</i> and <i>IDH2</i>, which indicated a poor prognosis for their therapy. Two glioblastomas carry the pathogenic mutation p.Arg110Pro in the gene <i>TP53.</i> All cell lines studied express RNA of tumor suppressor and oncogenic isoforms of the p73 protein. The glioblastomas responded differently to radiotherapy, with five of them being more resistant to γ irradiation than the standard A172 glioma line. All six cell lines express RNA genes for vascular endothelial growth factor and its receptor (VEGFR-1) in different ratios. Testing of an immunotherapeutic regimen with monoclonal antibodies to VEGFR-1 on one of the cell lines confirms that the studied glioblastomas are sensitive to blocking vascular growth factor and its receptor. Thus, these glioblastomas can become a promising model for studying the formation of tumor-cell resistance to radiotherapy and the effectiveness of immunotherapy that blocks growth factors and their receptors.</p></div>","PeriodicalId":716,"journal":{"name":"Nanotechnologies in Russia","volume":"19 2","pages":"282 - 290"},"PeriodicalIF":0.8000,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New Gliobastoma Cell Lines: Analysis of Genetic Changes, and Assessment of Sensitivity to Radiotherapy and Immunotherapy\",\"authors\":\"S. S. Emelianova, A. V. Volnitskiy, A. M. Solianik, N. H. Tran, L. A. Garaeva, R. A. Pantina, M. N. Grunina, E. D. Putevich, A. S. Potyseva, A. M. Golubev, V. S. Burdakov, N. A. Verlov, S. N. Naryzhnyy, A. L. Konevega, T. A. Shtam\",\"doi\":\"10.1134/S2635167624600871\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The characteristics of six new glioblastoma cell lines obtained from tumor material from patients are presented. The studied glioblastomas do not have mutations in the genes <i>IDH1</i> and <i>IDH2</i>, which indicated a poor prognosis for their therapy. Two glioblastomas carry the pathogenic mutation p.Arg110Pro in the gene <i>TP53.</i> All cell lines studied express RNA of tumor suppressor and oncogenic isoforms of the p73 protein. The glioblastomas responded differently to radiotherapy, with five of them being more resistant to γ irradiation than the standard A172 glioma line. All six cell lines express RNA genes for vascular endothelial growth factor and its receptor (VEGFR-1) in different ratios. Testing of an immunotherapeutic regimen with monoclonal antibodies to VEGFR-1 on one of the cell lines confirms that the studied glioblastomas are sensitive to blocking vascular growth factor and its receptor. Thus, these glioblastomas can become a promising model for studying the formation of tumor-cell resistance to radiotherapy and the effectiveness of immunotherapy that blocks growth factors and their receptors.</p></div>\",\"PeriodicalId\":716,\"journal\":{\"name\":\"Nanotechnologies in Russia\",\"volume\":\"19 2\",\"pages\":\"282 - 290\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2024-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanotechnologies in Russia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S2635167624600871\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanotechnologies in Russia","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1134/S2635167624600871","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Engineering","Score":null,"Total":0}
New Gliobastoma Cell Lines: Analysis of Genetic Changes, and Assessment of Sensitivity to Radiotherapy and Immunotherapy
The characteristics of six new glioblastoma cell lines obtained from tumor material from patients are presented. The studied glioblastomas do not have mutations in the genes IDH1 and IDH2, which indicated a poor prognosis for their therapy. Two glioblastomas carry the pathogenic mutation p.Arg110Pro in the gene TP53. All cell lines studied express RNA of tumor suppressor and oncogenic isoforms of the p73 protein. The glioblastomas responded differently to radiotherapy, with five of them being more resistant to γ irradiation than the standard A172 glioma line. All six cell lines express RNA genes for vascular endothelial growth factor and its receptor (VEGFR-1) in different ratios. Testing of an immunotherapeutic regimen with monoclonal antibodies to VEGFR-1 on one of the cell lines confirms that the studied glioblastomas are sensitive to blocking vascular growth factor and its receptor. Thus, these glioblastomas can become a promising model for studying the formation of tumor-cell resistance to radiotherapy and the effectiveness of immunotherapy that blocks growth factors and their receptors.
期刊介绍:
Nanobiotechnology Reports publishes interdisciplinary research articles on fundamental aspects of the structure and properties of nanoscale objects and nanomaterials, polymeric and bioorganic molecules, and supramolecular and biohybrid complexes, as well as articles that discuss technologies for their preparation and processing, and practical implementation of products, devices, and nature-like systems based on them. The journal publishes original articles and reviews that meet the highest scientific quality standards in the following areas of science and technology studies: self-organizing structures and nanoassemblies; nanostructures, including nanotubes; functional and structural nanomaterials; polymeric, bioorganic, and hybrid nanomaterials; devices and products based on nanomaterials and nanotechnology; nanobiology and genetics, and omics technologies; nanobiomedicine and nanopharmaceutics; nanoelectronics and neuromorphic computing systems; neurocognitive systems and technologies; nanophotonics; natural science methods in a study of cultural heritage items; metrology, standardization, and monitoring in nanotechnology.