Dataset. 2022

Protein-Functionalized Microgel for Multiple Myeloma Cells’ 3D Culture

RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
oai:riunet.upv.es:10251/189950
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
  • Marín Pallá, Juan Carlos
  • Clara Trujillo, Sandra
  • Cordón, Lourdes
  • Gallego Ferrer, Gloria
  • Sempere, Amparo
  • Gómez Ribelles, José Luís
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., 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.
 

DOI: http://hdl.handle.net/10251/189950, https://dx.doi.org/10.4995/Dataset/10251/189950
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
oai:riunet.upv.es:10251/189950

HANDLE: http://hdl.handle.net/10251/189950, https://dx.doi.org/10.4995/Dataset/10251/189950
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
oai:riunet.upv.es:10251/189950
 
Ver en: http://hdl.handle.net/10251/189950, https://dx.doi.org/10.4995/Dataset/10251/189950
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
oai:riunet.upv.es:10251/189950

RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
oai:riunet.upv.es:10251/192919
Artículo científico (article). 2022

PROTEIN-FUNCTIONALIZED MICROGEL FOR MULTIPLE MYELOMA CELLS' 3D CULTURE

RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
  • Marin-Paya, Juan Carlos
  • Clara-Trujillo, Sandra
  • Cordón, Lourdes
  • Gallego Ferrer, Gloria
  • Sempere, Amparo
  • Gómez Ribelles, José Luís
[EN] 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., This research was funded by the Generalitat Valenciana, grant number PROMETEO/2016/063; JLGR acknowledges that support by was funded by the Spanish State Research Agency (AEI) through the PID2019-106099RB-C41/AEI/10.13039/501100011033 project.



Ver en: 36359316