TGF-β-specific covalently closed antisense molecule

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

Reexamination Certificate

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C514S04400A, C536S025300

Reexamination Certificate

active

07420050

ABSTRACT:
The present application describes a purified covalently closed antisense molecule, which specifically inhibits expression of TGF-β.

REFERENCES:
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patent: 1239034 (2002-09-01), None
patent: WO 00/61595 (2000-10-01), None
patent: WO 00/61595 (2000-10-01), None
Han et al. Therapy with antisense TGF-B1 oligodeoxynucleotides reduces kidney weight and matrix mRNAs in diabetic mice. Apr. 2000. American Journal of Physiology-Renal Physiology. vol. 278. pp. F628-634.
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Moon et al. Potent growth inhibition of leukemic cells by novel ribbon-type antisense oligonucleotides to c-myb1. Feb. 2000. Journal of Biological Chemistry. vol. 275. pp. 4647-4653.
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Moon et al., “Target site search and effective inhibition of leukaemic cell growth by a covalently closed multiple anti-sense oligonucleotide to c-myb”, Biochem. J., 2000, 346: 295-303.
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Fitzpatrick et al., “Transforming Growth Factor-Beta:Antisense RNA-Mediated Inhibition Affects Anchorage-Independent Growth, Tumorigenicity and Tumor-Infiltrating T-Cells in Malignant Mesothelioma”, Growth Factors, 1994, 11: 29-44.
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Akagi et al., “Inhibition of TGF-Beta1 expression by antisense oligonucleotides suppressed extracellular matrix accumulation in experimental glomerulonephritis,” Kidney International, 50: 148-155 (1996).
Choi et al., “Prevention of tissue injury by ribbon antisense to TGF-Beta1 in the kidney,” International Journal of Molecular Medicine, 15: 391-399 (2005).
Isaka, Y., “Application of gene therapy to kidney diseases,” Clin Exp Nephrol, 3: 147-153 (1999).
Isaka et al., “Transforming growth factor-Beta1 antisense oligodeoxynucleotides block interstitial fibrosis in unilateral ureteral obstruction,” Kidney International, 58: 1885-1892 (2000).
Ando et al., “Introduction of TGF-beta antisense oligodeoxy-nucleotides (ODN) into interstitial fibroblast blocked tubulointerstitial fibrosis in unilateral ureter obstruction (UUO) rats,” Journal of Americal Society of Nephrology, 9: 512A (1998), abstract A2617.
Isaka Y et al., “Transforming growth factor-beta1 antisense oligodeoxynucleotides block interstitial fibrosis in unilateral ureteral obstruction,” Kidney International, 58(5):1885-1892 (2000).
Isaka Y, “Application of gene therapy to kidney diseases,” Clinical and Experimental Nephrology, 3:147-153 (1999).
Ando Y et al., “Introduction of TGF-beta antisense oligodeoxy-nucleotides (ODN) into interstitial fibroblast blocked tubulointerstitial fibrosis in unilateral ureter obstruction (UUO) rats,” Journal of the American Society of Nephrology, 9: 512A (1998).
Akagi Y et al., “Inhibition of TGF-beta 1 expression by antisense oligonucleotides suppressed extracellular matrix accumulation in experimental glomerulonephritis,” Kidney International 50(1) 148-155 (1996).
Moon et al., “Potent growth inhibition of leukemic cells by novel ribbon-type antisense oligonucleotides to c-myb1,” The Journal of Biological Chemistry, 275(7): 4647-4653 (2000).
Moon et al., “Target site search and effective inhibition of leukaemic cell growth by a covalently closed multiple anti-sense oligonucleotide to c-myb,” Biochem. J., 346:295-303 (2000).

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