International Journal of Oncology · 2006 · 25 citations · 16 references
MedicineOncologyPharmacologyCancer PharmacologyMolecular OncologyNeoplasiaMalignant NeoplasmsNoncoding Rna In CancerAntisense RnasCancer Cell Proliferation InhibitionColony-forming Unit AssaysGrowth Inhibition AssaysOligonucleotide TherapeuticsProtein Expression LevelsRibonucleotide Reductase RegulationTherapeutic Growth Inhibition
GTI-2501 is a 20-mer oligonucleotide that is complementary to a coding region in the mRNA of R1, the large subunit of ribonucleotide reductase (RNR). In vitro studies, have demonstrated that GTI-2501 decreases mRNA and protein levels of R1 in a sequence-specific and dose-dependent manner. Furthermore, GTI-2501 inhibits the growth of human lung, liver, ovary, brain, melanoma, breast and pancreatic tumor cells in colony forming assays. In vivo studies have shown that GTI-2501 significantly inhibits growth of human colon, pancreas, lung, breast, renal, ovarian, melanoma, brain glioblastoma-astrocytoma, and prostatic tumors in CD-1 nude, Balb/c nude and/or SCID mice. GTI-2501 treatment caused total regression of human breast and renal tumor xenografts in mice. These effects are not observed with a scrambled control oligonucleotide containing the same base content but not complementary to R1. GTI-2501 specifically inhibits metastasis of human melanoma cells to the lungs in CD-1 athymic nude mice and prolongs the survival of mice bearing human lymphoma. Taken together these results suggest that an antisense mechanism of action is responsible for growth inhibition in vitro and in vivo and that GTI-2501 can act as a selective and specific anti-tumor agent.
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A ribonucleotide reductase gene is a transcriptional target of p53 and p73
Katsunori Nakano, Éva Bálint, Margaret Ashcroft et al. · Oncogene · 2000 · 232 citations
p53R2-dependent pathway for DNA synthesis in a p53-regulated cell cycle checkpoint.
Tatsuya Yamaguchi, Koichi Matsuda, Yoji Sagiya et al. · PubMed · 2001 · 139 citations
Role of ribonucleotide reductase in expression of the neoplastic program
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