@misc{10818/62779,
year = {2024},
url = {http://hdl.handle.net/10818/62779},
abstract = {Objective: Vaccines for the deadliest brain tumor-glioblastoma (GBM)-are generally based on targeting growth factors or their receptors, often using antibodies. The vaccines described in the review were prepared to suppress the principal cancer growth factor-IGF-I, using anti-gene approaches either of antisense (AS) or of triple helix (TH) type. Our objective was to increase the median survival of patients treated with AS and TH cell vaccines. Methodology: The cells were transfected in vitro by both constructed IGF-I AS and IGF-I TH expression episomal vectors; part of these cells was co-cultured with plant phytochemicals, modulating IGF-I expression. Both AS and TH approaches completely suppressed IGF-I expression and induced MHC-1/B7 immunogenicity related to the IGF-I receptor signal. Results: This immunogenicity proved to be stronger in IGF-I TH than in IGF-I AS-prepared cell vaccines, especially in TH/phytochemical cells. The AS and TH vaccines generated an important TCD8+ and TCD8+CD11b-immune response in treated GBM patients and increased the median survival of patients up to 17-18 months, particularly using TH vaccines; in some cases, 2-and 3-year survival was reported. These clinical results were compared with those obtained in therapies targeting other growth factors. Conclusion: The anti-gene IGF-I vaccines continue to be applied in current GBM personalized medicine. Technical improvements in the preparation of AS and TH vaccines to increase MHC-1 and B7 immunogenicity have, in parallel, allowed to increase in the median survival of patients. © 2024 Bentham Science Publishers.},
publisher = {Current Medicinal Chemistry},
title = {Anti-Gene IGF-I Vaccines in Cancer Gene Therapy: A Review of a Case of Glioblastoma},
doi = {10.2174/0109298673237968231106095141},
author = {Trojan A. and Lone Y.-C. and Briceno I. and Trojan J.},
}