Fernando Mendes1, 2,,
Cátia Domingues3, 4,
Susann Schugk5,
Ana Margarida Abrantes1, 3,
Ana Cristina Gonçalves3, 4,
Tiago Sales1,
Ricardo Teixo1,
Rita Silva1,
Jéssica Estrela6,
Mafalda Laranjo1, 3,
João Casalta-Lopes1, 7,
Clara Rocha8, 9,
Paulo César Simões7,
Ana Bela Sarmento3, 10,
Maria Filomena Botelho1, 3,
Manuel Santos Rosa11 1Biophysics and Biomathematics Institute, IBILI-Faculty of Medicine, University of Coimbra, Portugal
2Polytechnic Institute of Coimbra, ESTESC-Coimbra Health School, Department Biomedical Laboratory Sciences, Coimbra, Portugal;CIMAGO, FMUC-Faculty of Medicine, University of Coimbra, Portugal;CNC.IBILI, Universidade de Coimbra, Portugal
3CIMAGO, FMUC-Faculty of Medicine, University of Coimbra, Portugal
4Oncobiology and Hematology Laboratory Applied Molecular Biology and Clinical University of Hematology, Faculty of Medicine of University of Coimbra, Coimbra, Portugal
5Biomedical Laboratory Sciences Department, University of Gothenburg
6Polytechnic Institute of Coimbra, ESTESC-Coimbra Health School, Department Biomedical Laboratory Sciences, Coimbra, Portugal
7Radiation Oncology Department, Hospital and University Center of Coimbra, Coimbra, Portugal
8Polytechnic Institute of Coimbra, ESTESC-Coimbra Health School, Department Complementary Sciences, Coimbra, Coimbra, Portugal
9Institute for Systems Engineering and Computers at Coimbra, Coimbra, Portugal
10Oncobiology and Hematology Laboratory Applied Molecular Biology and Clinical University of Hematology, Faculty of Medicine of University of Coimbra, Coimbra, Portugal;Hematology Clinic Department, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal
11Immunology Institute, Faculty of Medicine, University of Coimbra, Coimbra, Portugal
Journal of Cancer Research and Treatment.
2016,
Vol. 4 No. 1, 9-16
DOI: 10.12691/jcrt-4-1-2
Copyright © 2016 Science and Education PublishingCite this paper: Fernando Mendes, Cátia Domingues, Susann Schugk, Ana Margarida Abrantes, Ana Cristina Gonçalves, Tiago Sales, Ricardo Teixo, Rita Silva, Jéssica Estrela, Mafalda Laranjo, João Casalta-Lopes, Clara Rocha, Paulo César Simões, Ana Bela Sarmento, Maria Filomena Botelho, Manuel Santos Rosa. Single Shot Irradiation and Molecular Effects on a Diffuse Large B Cell Lymphoma Cell Line.
Journal of Cancer Research and Treatment. 2016; 4(1):9-16. doi: 10.12691/jcrt-4-1-2.
Correspondence to: Fernando Mendes, Biophysics and Biomathematics Institute, IBILI-Faculty of Medicine, University of Coimbra, Portugal. Email:
fjmendes@estescoimbra.ptAbstract
Background: Diffuse large B cell lymphoma (DLBCL) is recognized as a heterogeneous group of hematological malignancies, and collectively forms the most common type of aggressive, non-Hodgkin lymphoma. The aim of our study was to evaluate the cellular and molecular effects of high doses X radiation in a DLBCL cell line. Materials and Methods: Farage cells were cultured and exposed to 0.5-60 Gy of Ionizing Radiation (IR). Cell viability and proliferation were assessed by trypan blue assay. Cell survival was determined with clonogenic assay. Cell death was assessed by flow cytometry (FC) and by optical microscopy. Cell cycle, mitochondrial membrane potential, reactive oxygen species, GSH and BAX/BCL-2 ratio were measured by FC. DNA damage was evaluated using comet assay. Total and phosphorylated P53 was assessed by western blot. Results: IR induced cytotoxic and cytostatic effects in Farage cells in a dose and time dependent manner with an LD50 of 1.73 Gy. Cell death occurs mainly by apoptosis or later apoptosis/necrosis with an increase in BAX/BCL-2 ratio and a significant increase in ROS production. We also observed cell cycle arrest at G2/M phase and a significant increase in DNA damage as well as P53 total and phosphorylated expression levels. Conclusions: High doses of IR induces a time and dose dependent response which leads to increased ROS production, DNA damage with the increased P53 expression and activation expressed by elevated levels of pP53, resulting in G2/M cell cycle arrest and increases in later apoptosis/necrosis cell death. Our results showed that single shot IR induces effects in different cell components and its comprehension is essential to choose the treatment planning.
Keywords