Marinella N. Ghezzo (CBMR, Faro), Mónica T. Fernandes (CBMR, Faro), Ivette Pacheco-Leyva (i3S, Porto), Pedro M. Rodrigues (i3S, Porto), Rui S. Machado (CBMR, Faro), Marta A.S. Araújo (i3S, Porto), Ravi K. Kalathur (CBMR, Faro), Matthias E. Futschik (CBMR, Faro; CCMAR, Faro; ITSMED, Plymouth), Nuno L. Alves (i3S, Porto), Nuno R. dos Santos (CBMR, Faro; i3S, Porto),
Specific gene silencing was vectorized via gold nanoparticles to enhance the killing potential of chemotherapy against leukemia cells. By targeting the fusion oncogene BCR-ABL1 using gold nanoaprticles in chronic myeloid leukemia cells, the Portuguese researchers were capable to enhance the therapeutic efficacy of standard chemotherapy in a combined strategy that this groups has been optimizing at UCIBIO (Research Unit on Applied Molecular Biosciences), Faculdade de Ciências e Tecnologia of Universidade Nova de Lisboa.
Mónica T. Fernandes1,2, Marinella N. Ghezzo1,2, André B. Silveira3, Ravi K. Kalathur1, Vanda Póvoa4, Ana R. Ribeiro5,6,7, Sílvia R. Brandalise3, Emmanuel Dejardin8, Nuno L. Alves5,6, Jacques Ghysdael 9,10,11, João T. Barata4, José Andres Yunes3,12, and Nuno R. dos Santos1
In this study we identified a population of human mesenchymal stem cells capable of expanding the number of hematopoietic stem cells in laboratory. Hematopoietic stem cells reside in the bone marrow and are responsible for producing all the blood and immune cells necessary for survival. However, this group of cells is extremely rare, which limits their usage in clinical transplantations.
In this study we identified a population of human mesenchymal stem cells capable of expanding the number of hematopoietic stem cells in laboratory. Hematopoietic stem cells reside in the bone marrow and are responsible for producing all the blood and immune cells necessary for survival. However, this group of cells is extremely rare, which limits their usage in clinical transplantations.