Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai
Reexamination Certificate
2004-06-03
2009-06-02
McGarry, Sean R (Department: 1635)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Carbohydrate doai
C435S006120, C435S375000, C435S377000, C536S023100, C536S024100, C536S024500
Reexamination Certificate
active
07541344
ABSTRACT:
Compounds and compositions are provided for modulating the expression of survivin. The compounds, exemplified by those acting through an RNAi antisense mechanism of action, include double-stranded and single-stranded constructs, as well as siRNAs, canonical siRNAs, blunt-ended siRNAs and single-stranded antisense RNA compounds. Methods of using these compounds for modulation of survivin expression and for treatment of diseases associated with expression of survivin are provided.
REFERENCES:
patent: 3687808 (1972-08-01), Merigan et al.
patent: 5808036 (1998-09-01), Kool
patent: 5898031 (1999-04-01), Crooke
patent: 6060456 (2000-05-01), Arnold et al.
patent: 6077709 (2000-06-01), Bennett et al.
patent: 6107094 (2000-08-01), Crooke
patent: 6165788 (2000-12-01), Bennett et al.
patent: 6245523 (2001-06-01), Altieri
patent: 6335194 (2002-01-01), Bennett et al.
patent: 6509162 (2003-01-01), Altieri
patent: 6656684 (2003-12-01), Sandler
patent: 6777444 (2004-08-01), Huang et al.
patent: 6838283 (2005-01-01), Bennett et al.
patent: 7288530 (2007-10-01), Bennett et al.
patent: 2002/0068708 (2002-06-01), Wengel et al.
patent: 2002/0132788 (2002-09-01), Lewis et al.
patent: 2002/0137708 (2002-09-01), Bennett et al.
patent: 2002/0160393 (2002-10-01), Symonds et al.
patent: 2003/0206887 (2003-11-01), Morrissey et al.
patent: 2003/0211607 (2003-11-01), Bennett et al.
patent: 2004/0018999 (2004-01-01), Beach et al.
patent: 2004/0259247 (2004-12-01), Tuschl et al.
patent: 2005/0100907 (2005-05-01), Kreutzer et al.
patent: 2005/0143335 (2005-06-01), Bennett et al.
patent: WO 99/14226 (1999-03-01), None
patent: WO 99/32619 (1999-07-01), None
patent: WO 00/18781 (2000-04-01), None
patent: WO 00/44914 (2000-08-01), None
patent: WO 00/49035 (2000-08-01), None
patent: WO 01/29058 (2001-04-01), None
patent: WO 01/36641 (2001-05-01), None
patent: WO 01/36646 (2001-05-01), None
patent: WO 01/48183 (2001-07-01), None
patent: WO 01/57059 (2001-08-01), None
patent: WO 01/75164 (2001-10-01), None
patent: WO 02/44321 (2002-06-01), None
Vickers et al. The Journal of Biological Chemistry vol. 278(9):7108-7118, 2003.
Adida et al., “Anti-apoptosis gene, surviving, and prognosis of neuroblastoma,”The Lancet, Vo. 351, pp. 882-883 (1998).
Altieri, Dario, “Xa receptor EPR-1,”FASEB, vol. 9, pp. 860-865 (1995).
Altieri, Dario, “Splicing of Effector Cell Protease Receptor-1 mRNA Is Modulated by an Unusual Retained Intron,”Biochemistry, vol. 33, pp. 13848-13855 (1994).
Amarzguioui et al., “Tolerance for mutations and chemical modifications in a siRNA,”Nucleic Acids Research, 31:2, pp. 589-595 (2003).
Ambrosini et al., “Induction of Apoptosis and Inhibition of Cell Proliferation bysurvivingGene Targeting,”J. of Biological Chemistry, 273:18, pp. 11177-11182 (1998).
Ambrosini et al., “A novel anti-apoptosis gene,surviving, expressed in cancer and lymphoma,”Nature Medicine, 3:8, pp. 917-921 (1997).
Bass, Brenda, “Double-Stranded RNA as a Template for Gene Silencing,”Cell, vol. 101, pp. 235-238 (2000).
Boutla et al., “Short 5′-phosphorylated double-stranded RNAs induce RNA interference inDrosophila,” Current Biology, vol. 11, pp. 1776-1780 (2001).
Branch, Andrea, “A good antisense molecule is hard to find,”TIBS, vol. 23, pp. 45-50 (1998).
Brantl, Sabine, “Antisense-RNA regulation and RNA interference,”Bioehimica et Biophysica Acta, vol. 1575, pp. 15-25 (2002).
Caplen et al., “Specific inhibition of gene expression by small double-stranded RNAs in invertebrate and vertebrate systems,”PNAS, 98:17, pp. 9742-9747 (2001).
Carmell et al., “The Argonaute family: tentacles that reach into RNAi, developmental control, stem maintenance, and tumorigenesis,”Genes&Development, vol. 16, pp. 2733-2742 (2002).
Chui et al., “RNAi in Human Cells: Basic Structural and Functional Features of Small Interfering RNA,”Molecular Cell, vol. 10, pp. 549-561 (2002).
Cogoni et al., “Post-transcriptional gene silencing across kingdoms,”Curr. Opinion in Genes Dev., vol. 10, pp. 638-643 (2000).
Cohen, Gerald, “Caspases: the executioners of apoptosis,”Biochem. J., vol. 326, pp. 1-16 (1997).
Czauderna et al., “Structural variations and stabilising modifications of synthetic siRNAs in mammalian cells,”Nucleic Acids Research, 31:11, 2705-2716 (2003).
Elbashir et al., “Functional anatomy of siRNAs for mediating efficient RNAi inDrosophila melanogasterembryo lysate,”The EMBO Journal, 20:23, pp. 6877-6888 (2001).
Elbashir et al., “RNA interference is mediated by 21- and 22-nucleotide RNAs,”Genes&Development, vol. 15, pp. 188-200 (2001).
Elbashir, et al., “Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells,”Nature, vol. 411, pp. 494-498 (2001).
Fire et al., “Potent and specific genetic interference by double-stranded RNA inCaenorhabditis elegans,” Nature, vol. 391, pp. 806-811 (1998).
Genbank Accession No. AW247335, Dec. 16, 1999.
Grossman et al., “Expression of the Apoptosis Inhibitor, Survivin, in Nonmelanoma Skin Cancer and Gene Targeting in a Keratinocyte Cell Line,”Laboratory Investigation, United States and Canadian Academy of Pathology, 79:CX9, pp. 1121-1126 (1999).
Guo et al., “par-1, a Gene Required for Establishing Polarity inC. elegansEmbryos, Encodes a Putative Ser/Thr Kinase That Is Asymmetrically Distributed,”Cell, vol. 81, pp. 611-620 (1995).
Gura, Trisha, “A silence that speaks volumes,”Nature, vol. 404, pp. 804-808 (2000).
Jen et al., “Suppression of Gene Expression by Targeted Disruption of Messange RNA: Available Options and Current Strategies,”Stem Cells, vol. 18, pp. 307-319 (2000).
Kawasaki et al., “Uniformly Modified 2′-Deoxy-2′-fluoro Phosphorothioate Oligonucleotides as Nucleas-Resistant Antisense Compounds with High Affinity and Specificity for RNA Targets,”J. Med. Chem., vol. 36, pp. 831-841 (1993).
Kawasaki et al., “Synthesis and Biophysical Studies of 2′-dRibo-2′-F Modified Oligonucleotides,” ISIS Pharmaceuticals, Inc., 2280 Faraday Avenue, Carlsbad, CA 92008, USA (1991).
Li et al., “Control of apoptosis and mitotic spindle checkpoint by surviving,”Nature, vol. 396, pp. 580-584 (1998).
Li et al., “Pleiotropic cell-division defects and apoptosis induced by interference with surviving function,”Nature Cell Biology, vol. 1, pp. 461-466 (1999).
Lu et al., “Expression of a Novel Antiapoptosis Gene, Survivin, Correlated with Tumor Cell Apoptosis and p53 Accumulation in Gastric Carcinomas,”Cancer Research, vol. 58, pp. 1808-1812 (1998).
Martinez et al., “Single-Stranded Antisense siRNAs Guide Target RNA Cleavage in RNAi,”Cell, vol. 110, pp. 563-574 (2002).
Metelev et al., “Study of Antisense Oligonucleotide Phosphorothioates Containing Segments of Oligodeoxynucleotides and 2′-O-Methyloligoribonucleotides,”Bioorganic&Medicinal Chemistry Letters, 4:24, pp. 2929-2934 (1994).
Monia et al., “Evaluation of 2′-Modified Oligonucleotides Containing 2′-Deoxy Gaps as Antisense Inhibitors of Gene Expression,”J. of Biological Chemistry, 268:19, pp. 14514-14522 (1993).
Montgomery et al., “RNA as a target of double-stranded RNA-mediated genetic interference inCaenorhabditis elegans,” Proc. Natl. Acad. Sci., vol. 95, pp. 15502-15507 (1998).
Paddison et al., “Stable suppression of gene expression by RNAi in mammalian cells,”PNAS, 99:3, pp. 1443-1448 (2002).
Parrish et al., “Functional Anatomy of a dsRNA Trigger: Differential Requirement for the Two Trigger Strands in RNA Interference,”Molecular Cell, vol. 6, pp. 1077-1087 (2000).
Schwarz et al., “Evidence that siRNAs Function as Guides, Not Primers, in theDrosophilaand Human RNAi Pathways,”Molecular Cell, vol.
Bhat Balkrishen
Patel Bharvin Kumar
Swayze Eric
Cohen Charles E.
Desai Manisha A.
Eli Lilly and Company
ISIS Pharmaceuticals Inc.
McGarry Sean R
LandOfFree
Modulation of survivin expression does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Modulation of survivin expression, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Modulation of survivin expression will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-4077864