US2011054006A1PendingUtilityA1

Regulation of oncogenes by micrornas

Assignee: UNIV YALEPriority: Sep 2, 2004Filed: Apr 26, 2010Published: Mar 3, 2011
Est. expirySep 2, 2024(expired)· nominal 20-yr term from priority
A61P 35/02A61P 5/00A61P 43/00A61P 35/00A61P 25/00A61P 1/04A61P 21/00A61P 13/10A61P 15/00A61P 1/02C12N 15/1136C12N 2310/141A61P 19/00A61P 11/00C12N 15/1138A61P 1/16A61P 17/00A61K 31/7088C12N 15/1135C12N 2310/111A61K 48/00A61P 1/18A61P 13/08A61K 41/00A61K 38/00A61K 45/06
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Claims

Abstract

Naturally occurring miRNAs that regulate human oncogenes and methods of use thereof are described. Suitable nucleic acids for use in the methods and compositions described herein include, but are not limited to, pri-miRNA, pre-miRNA, mature miRNA or fragments of variants thereof that retain the biological activity of the mature miRNA and DNA encoding a pri-miRNA, pre-miRNA, mature miRNA, fragments or variants thereof, or regulatory elements of the miRNA. The compositions are administered to a subject prior to administration of a cytotoxic therapy in an amount effective to sensitize cells or tissues to be treated to the effects of the cytotoxic therapy.

Claims

exact text as granted — not AI-modified
1 . A method for increasing the sensitivity of a cell to cytotoxic therapy comprising administering one or more miRNAs to a patient, and subsequently administering a chemotherapeutic agent or radiation, wherein the one or more miRNAs are administered in an amount effective to sensitize the cells or tissues to be treated to the cytotoxic therapy. 
     
     
         2 - 24 . (canceled)

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