IGF-I Antisense and Triple-Helix Gene Therapy of Glioblastoma

نویسندگان

  • Jerzy Trojan
  • Ignacio Briceno
چکیده

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Human glioma cells transformed by IGF-I triple helix technology show immune and apoptotic characteristics determining cell selection for gene therapy of glioblastoma.

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IGF-I triple helix gene therapy of rat and human gliomas.

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Papers Human glioma cells transformed by IGF-I triple helix technology show immune and apoptotic characteristics determining cell selection for gene therapy of glioblastoma

Aims—Insulin-like growth factor type I (IGF-I) antisense cellular gene therapy of tumours is based on the following data: rat glioma or hepatoma cells transfected with the vector encoding IGF-I antisense cDNA lose their tumorigenicity and induce a tumour specific immune response involving CD8 T cells. Recently, using the IGF-I triple helix approach in studies of tumorigenicity, major histocompa...

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IGF-I: from diagnostic to triple-helix gene therapy of solid tumors.

Alterations in the expression of growth factors and their receptors are associated with the growth and development of human tumors. One such growth factor is IGF-I (insulin-like growth factor I ), a 70-amino-acid polypeptide expressed in many tissues, including brain. IGF-I is also expressed at high levels in some nervous system-derived tumors, especially in glioblastoma. When using IGF-I as a ...

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Erratum to “Methodology for Anti-Gene Anti-IGF-I Therapy of Malignant Tumours”

The aim of this study was to establish the criteria for methodology of cellular "anti-IGF-I" therapy of malignant tumours and particularly for glioblastoma multiforme. The treatment of primary glioblastoma patients using surgery, radiotherapy, and chemotherapy was followed by subcutaneous injection of autologous cancer cells transfected by IGF-I antisense/triple helix expression vectors. The pr...

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تاریخ انتشار 2017