eng Science and Education Publishing Journal of Cancer Research and Treatment 2374-2003 2016-03-03 4 1 9 16 10.12691/jcrt-4-1-2 JCRT2016412 article Fernando Mendes 1 2 3 4 Cátia Domingues 4 5 Susann Schugk 6 Ana Margarida Abrantes 6 6 Ana Cristina Gonçalves 6 6 Tiago Sales 6 Ricardo Teixo 6 Rita Silva 6 Jéssica Estrela 6 Mafalda Laranjo 6 6 João Casalta-Lopes 6 7 Clara Rocha 8 9 Paulo Cãsar Simões 9 Ana Bela Sarmento 9 9 10 Maria Filomena Botelho 10 10 Manuel Santos Rosa 11 Biophysics and Biomathematics Institute, IBILI-Faculty of Medicine, University of Coimbra, Portugal Biomedical Laboratory Sciences Department, University of Gothenburg Polytechnic Institute of Coimbra, ESTESC-Coimbra Health School, Department Complementary Sciences, Coimbra, Coimbra, Portugal 1Immunology Institute, Faculty of Medicine, University of Coimbra, Coimbra, Portugal 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. http://pubs.sciepub.com/jcrt/4/1/2/jcrt-4-1-2.pdf large diffuse B cell lymphoma radiotherapy genotoxicity oxidative stress cell death P53