Glioblastomas (GBMs) are very aggressive and almost incurable brain tumors. The development of new therapeutical approaches capable of selectively killing cancer cells could represent a step forward to fight cancer. With this aim we tested the efficacy of a novel oncolytic therapy based on recombinant herpes simplex viruses (HSVs) infecting exclusively cells expressing the human receptor HER-2 [1, 2], overexpressed in about 15% of GBMs [3]. For this study we exploited a murine GBM model based on PDGF-B embryonic transduction [4, 5]. We engineered cell cultures derived from this model to express HER-2 and we injected intracranically such cultures in NOD/SCID mice. We evaluated the efficacy of R-LM113, a recombinant HSV directed to HER-2, in this glioma model expressing HER-2. We demonstrated that mice injected with engineered glioma cells infected with R-LM113 developed gliomas with a statistically significant delay compared to mice injected with non-infected engineered glioma cells.
Gambini E., Reisoli E., Appolloni I., Menotti L., Malatesta P. (2011). A murine model for virotherapy of malignant brain tumors. JOURNAL OF BIOLOGICAL RESEARCH, 84, 83-84.
A murine model for virotherapy of malignant brain tumors.
MENOTTI, LAURA;
2011
Abstract
Glioblastomas (GBMs) are very aggressive and almost incurable brain tumors. The development of new therapeutical approaches capable of selectively killing cancer cells could represent a step forward to fight cancer. With this aim we tested the efficacy of a novel oncolytic therapy based on recombinant herpes simplex viruses (HSVs) infecting exclusively cells expressing the human receptor HER-2 [1, 2], overexpressed in about 15% of GBMs [3]. For this study we exploited a murine GBM model based on PDGF-B embryonic transduction [4, 5]. We engineered cell cultures derived from this model to express HER-2 and we injected intracranically such cultures in NOD/SCID mice. We evaluated the efficacy of R-LM113, a recombinant HSV directed to HER-2, in this glioma model expressing HER-2. We demonstrated that mice injected with engineered glioma cells infected with R-LM113 developed gliomas with a statistically significant delay compared to mice injected with non-infected engineered glioma cells.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
