DOI:
https://doi.org/10.14483//udistrital.jour.RC.2016.25.a6Published:
08/31/2016Issue:
Vol. 25 No. 2 (2016): May-August 2016Section:
Science and EngineeringEpistemológica experiencia en la elaboración de tecnología biomolecular para estrategia de la inmunoterapia génica
Epistemological experience in developing of biomolecular technology for immunogene therapy strategy
Keywords:
antisens, triple helix, IGF-I, glioma, CD8 (en).Keywords:
antisentido, triple hélice, IGF-I, glioma, CD8 (es).Downloads
Abstract (es)
Unos de los retos científicos de los últimos 40 años, ha sido la búsqueda de la herramienta para el tratamiento del tumor cerebral, el glioblastoma, mortales en el 100% de los casos, utilizando nuestro conocimiento de la evolución, la química de las proteínas, la genética, la biología molecular y la inmunología. Una estrategia eficiente enfocada hacia el factor de crecimiento IGF-I presente en el desarrollo tumoral, fue establecida mediante la construcción de vectores expresando el IGF-I antisentido ARN o el IGF-I ARN formando ARN-ADN triple hélice. Estos vectores introducidos en las células cancerosas in vitro, permiten detener por completo la síntesis de IGF-I en la traducción o a nivel de la transcripción respectivamente. Mientras la inyección in vivo, inducen efecto antitumoral inmune (TCD8+) acompañado de aumento de la supervivencia media de los pacientes. La primera tesis en Colombia que describe la tecnología utilizada, fue presentada en la Universidad Distrital, en febrero de 2016.
Abstract (en)
We have been faced with a 40 year long challenge: how to establish tools that can be applied in the treatment of brain tumor - glioblastoma (100% fatal) - using our knowledge of evolution, chemistry of proteins, genetics, molecular biology and immunology. An efficient strategy targeting growth factor IGF-I, present in tumor development, was established by construction of vectors expressing either IGF-I antisense RNA or IGF-I RNA forming RNA-DNA triple helix. The vectors introduced in the cancer cells in vitro, enable to completely stop the synthesis of IGF-I: on translation or transcription level, respectively. When injected in vivo, these cells induce an immune anti-tumor effect (CD8+) accompanied by increase of the median survival of patients. The first thesis in Colombia describing the used technology, was presented in Distrital University in February 2016.
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