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.