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- W1036372864 abstract "3798 Background: Malignant gliomas are highly lethal tumors that display resistance to current therapies. The best treatment modality currently available for these tumors is a combination of maximal surgical resection followed by radiation therapy and concurrent temozolomide, an oral alkylating imidazotetrazine derivative. Although this combination has demonstrated activity, development of resistance and disease progression is common. Thus, additional agents to augment the effectiveness of this approach are needed. The presence of increased Ras signaling in malignant glioma offers a potential novel target. We now report the in vitro and orthotopic in vivo results of combination therapy using irradiation, temozolomide and SCH66336, an oral farnesyl transferase inhibitors, in a murine model of glioblastoma multiforme (GBM). Methods: To examine the activity of radiation, temozolomide, and SCH66336 U87 in vitro and in U87-induced intracranial tumors in SCID or nude mice were evaluated following treatment combinations. Experimental regimens included vehicle control, radiation and temozolomide (2.5Gy/day for 2 days, 5mg/kg/day 90 min prior to radiation), or SCH66336 (80 mg/kg SCH66336 by oral gavage once daily) alone and in combination with SCH66336. Endpoints evaluated included cell number, proliferation index, apoptotic index, and Ras activation. After completion of the experiment (defined as control or treated animals with symptomatic disease), animals were evaluated by MRI (T1, T2, T1 + gadolinium), sacrificed, and the brains perfused. Sections (5um) including tumor and adjacent brain were prepared and stained for CD31, Ki67 and an apoptotic marker. Results: As previously reported, radiation and concurrent temozolomide can induce significant cellular damage as demonstrated by proliferation inhibition and apoptosis. Similarly, SCH66336 independently inhibited Ras pathway signaling as determined by the activity of Ras isotypes and activation of downstream targets. SCH66336 alone had limited ability to inhibit orthotopic U87 tumors (T/C of 0.67), while the combination of radiation and temozolomide produced significant inhibition (T/C of 0.42). With concurrent SCH66336, radiation, and temozolomide, a decrease in T/C of 0.02 was observed with the majority of animals demonstrating a decrease in tumor volume (p" @default.
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- W1036372864 date "2006-04-15" @default.
- W1036372864 modified "2023-09-22" @default.
- W1036372864 title "SCH66336 (Sarasar®), an oral farnesyl transferase inhibitor, synergizes with temozolomide and radiation therapy for orthotopic malignant gliomas" @default.
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