Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture
Multiple myeloma is a hematologic neoplasm caused by an uncontrolled clonal proliferation of neoplastic plasma cells (nPCs) in the bone marrow. The development and survival of this disease is tightly related to the bone marrow environment. Proliferation and viability of nPCs depend on their interact...
| Authors: | , , , , , |
|---|---|
| Format: | conjunto de datos |
| Publication Date: | 2022 |
| Country: | España |
| Institution: | Universitat Politècnica de València (UPV) |
| Repository: | RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia |
| Language: | English |
| OAI Identifier: | oai:riunet.upv.es:10251/189950 |
| Online Access: | https://riunet.upv.es/handle/10251/189950 |
| Access Level: | Open access |
| Keyword: | Multiple myeloma Microgels Fibronectin Bortezomib Dexamethasone CIENCIA DE LOS MATERIALES E INGENIERIA METALURGICA |
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Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D CultureMarín Pallá, Juan CarlosCordón, LourdesSempere, AmparoClara-Trujillo, Sandra|||0000-0002-6455-2993Gallego-Ferrer, Gloria|||0000-0002-2428-0903Gómez Ribelles, José Luís|||0000-0001-9099-0885Multiple myelomaMicrogelsFibronectinBortezomibDexamethasoneCIENCIA DE LOS MATERIALES E INGENIERIA METALURGICAMultiple myeloma is a hematologic neoplasm caused by an uncontrolled clonal proliferation of neoplastic plasma cells (nPCs) in the bone marrow. The development and survival of this disease is tightly related to the bone marrow environment. Proliferation and viability of nPCs depend on their interaction with the stromal cells and the extracellular matrix components, which also influences the appearance of drug resistance. Recapitulating these interactions in an in vitro culture requires 3D environments that incorporate the biomolecules of interest. In this work, we studied the proliferation and viability of three multiple myeloma cell lines in a microgel consisting of biostable microspheres with fibronectin (FN) on their surfaces. We also showed that the interaction of the RPMI8226 cell line with FN induced cell arrest in the G0/G1 cell cycle phase. RPMI8226 cells developed a significant resistance to dexamethasone, which was reduced when they were treated with dexamethasone and bortezomib in combination.CIBER-BBN is an initiative funded by the VI National R&D&I Plan 2008–2011, Iniciativa Ingenio 2010, and Consolider Program. CIBER Actions were financed by the Instituto de Salud Carlos III, with assistance from the European Regional Development Fund. The kind supplying of RPMI 8226 cells by Beatriz Martin (Josep Carreras Leukaemia Research Institute) is greatly acknowledged. The Microscopy Service of the UPV (Universitat Politècnica de València) is gratefully acknowledged.MDPIUniversitat Politècnica de ValènciaDepartamento de Termodinámica AplicadaCentro de Biomateriales e Ingeniería TisularEscuela Técnica Superior de Ingeniería IndustrialInstituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo TecnológicoEscuela Técnica Superior de Ingeniería Agronómica y del Medio NaturalAgencia Estatal de InvestigaciónGeneralitat ValencianaRepositorio Institucional de la Universitat Politècnica de València Riunet20222022-11-21datasethttp://purl.org/coar/resource_type/c_ddb1VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/datasetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheetapplication/vnd.openxmlformats-officedocument.spreadsheetml.sheettext/plainhttps://riunet.upv.es/handle/10251/189950reponame:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valénciainstname:Universitat Politècnica de València (UPV)InglésengAgencia Estatal de Investigación http://dx.doi.org/10.13039/501100011033 Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020 PID2019-106099RB-C41 MICROGELES BIOMIMETICOS PARA EL ESTUDIO DE LA GENERACION DE RESISTENCIAS A FARMACOS EN EL MIELOMA MULTIPLEGeneralitat Valenciana https://doi.org/10.13039/501100003359 PROMETEO%2F2016%2F063 MEDULA OSEA ARTIFICIAL PARA PERSONALIZAR EL TRATAMIENTO DE PACIENTES DE CANCERES DE SANGREopen accesshttp://purl.org/coar/access_right/c_abf2Reconocimiento (by)http://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:riunet.upv.es:10251/1899502026-06-13T07:49:27Z |
| dc.title.none.fl_str_mv |
Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture |
| title |
Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture |
| spellingShingle |
Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture Marín Pallá, Juan Carlos Multiple myeloma Microgels Fibronectin Bortezomib Dexamethasone CIENCIA DE LOS MATERIALES E INGENIERIA METALURGICA |
| title_short |
Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture |
| title_full |
Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture |
| title_fullStr |
Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture |
| title_full_unstemmed |
Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture |
| title_sort |
Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture |
| dc.creator.none.fl_str_mv |
Marín Pallá, Juan Carlos Cordón, Lourdes Sempere, Amparo Clara-Trujillo, Sandra|||0000-0002-6455-2993 Gallego-Ferrer, Gloria|||0000-0002-2428-0903 Gómez Ribelles, José Luís|||0000-0001-9099-0885 |
| author |
Marín Pallá, Juan Carlos |
| author_facet |
Marín Pallá, Juan Carlos Cordón, Lourdes Sempere, Amparo Clara-Trujillo, Sandra|||0000-0002-6455-2993 Gallego-Ferrer, Gloria|||0000-0002-2428-0903 Gómez Ribelles, José Luís|||0000-0001-9099-0885 |
| author_role |
author |
| author2 |
Cordón, Lourdes Sempere, Amparo Clara-Trujillo, Sandra|||0000-0002-6455-2993 Gallego-Ferrer, Gloria|||0000-0002-2428-0903 Gómez Ribelles, José Luís|||0000-0001-9099-0885 |
| author2_role |
author author author author author |
| dc.contributor.none.fl_str_mv |
Departamento de Termodinámica Aplicada Centro de Biomateriales e Ingeniería Tisular Escuela Técnica Superior de Ingeniería Industrial Instituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natural Agencia Estatal de Investigación Generalitat Valenciana Repositorio Institucional de la Universitat Politècnica de València Riunet |
| dc.subject.none.fl_str_mv |
Multiple myeloma Microgels Fibronectin Bortezomib Dexamethasone CIENCIA DE LOS MATERIALES E INGENIERIA METALURGICA |
| topic |
Multiple myeloma Microgels Fibronectin Bortezomib Dexamethasone CIENCIA DE LOS MATERIALES E INGENIERIA METALURGICA |
| description |
Multiple myeloma is a hematologic neoplasm caused by an uncontrolled clonal proliferation of neoplastic plasma cells (nPCs) in the bone marrow. The development and survival of this disease is tightly related to the bone marrow environment. Proliferation and viability of nPCs depend on their interaction with the stromal cells and the extracellular matrix components, which also influences the appearance of drug resistance. Recapitulating these interactions in an in vitro culture requires 3D environments that incorporate the biomolecules of interest. In this work, we studied the proliferation and viability of three multiple myeloma cell lines in a microgel consisting of biostable microspheres with fibronectin (FN) on their surfaces. We also showed that the interaction of the RPMI8226 cell line with FN induced cell arrest in the G0/G1 cell cycle phase. RPMI8226 cells developed a significant resistance to dexamethasone, which was reduced when they were treated with dexamethasone and bortezomib in combination. |
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2022 |
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2022 2022-11-21 |
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Inglés eng |
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Inglés |
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Agencia Estatal de Investigación http://dx.doi.org/10.13039/501100011033 Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020 PID2019-106099RB-C41 MICROGELES BIOMIMETICOS PARA EL ESTUDIO DE LA GENERACION DE RESISTENCIAS A FARMACOS EN EL MIELOMA MULTIPLE Generalitat Valenciana https://doi.org/10.13039/501100003359 PROMETEO%2F2016%2F063 MEDULA OSEA ARTIFICIAL PARA PERSONALIZAR EL TRATAMIENTO DE PACIENTES DE CANCERES DE SANGRE |
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