Cytopathic adenoviral E1B mutated viruses for therapy and prophy

Chemistry: molecular biology and microbiology – Animal cell – per se ; composition thereof; process of...

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4353201, 536 2372, C07H 2104, C12N 510

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active

060805781

ABSTRACT:
Methods and compositions for treating neoplastic conditions by viral-based therapy are provided. Mutant virus lacking viral proteins which bind and/or inactivate p53 or RB are administered to a patient having a neoplasm which comprises cells lacking p53 and/or RB function. The mutant virus is able to substantially produce a replication phenotype in neoplastic cells but is substantially unable to produce a replication phenotype in non-replicating, non-neoplastic cells having essentially normal p53 and/or RB function. The preferential generation of replication phenotype in neoplastic cells results in a preferential killing of the neoplastic cells, either directly or by expression of a cytotoxic gene in cells expressing a viral replication phenotype.

REFERENCES:
patent: 5677178 (1997-10-01), McCormick

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