US008940711B2 a2) United States Patent (10) Patent No.: US 8,940,711 B2 Olsonet al. (45) Date of Patent: Jan. 27, 2015 (54) MICRO-RNA FAMILY THAT MODULATES C1I2N 2310/321 (2013.01); C12N 2310/346 FIBROSIS AND USES THEREOF (2013.01); CI2N 2310/3515 (2013.01); C12N (71) Applicant: The Board of Regents, The University 2320/31 (2013.01); CI2N 2330/10 (2013.01) of Texas System, Austin, TX (US) USPC iececcsesseeseeesenensceesensessecsenesenscnseeee 514/444 (58) Field of Classification Search (72) Inventors: Erie N. Olson, Dallas, TX (US); Eva USPC iececcsesseeseeesenensceesensessecsenesenscnseeee 514/44A van Rooij, Utrecht (NL) See application file for complete search history. (56) References Cited (73) Assignee: The Board of Regents, The University of Texas System, Austin, TX (US) U.S. PATENT DOCUMENTS Notice: Subject to any disclaimer, the term of this 7,232,806 B2 6/2007 Tuschletal. 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FOREIGN PATENT DOCUMENTS (60) Provisional application No. 60/952,917, filed on Jul. 31, 2007, provisional application No. 60/980,303, EP 1440981 A2 7/2004 filed on Oct. 16, 2007, provisional application No. EP 1627925 Al 2/2006 61/047,014,filed on Apr. 22, 2008. (Continued) OTHER PUBLICATIONS (51) Int. Cl. CIQN 15/11 (2006.01) Cheng et al, “MicroRNAs Are Aberrantly Expressed in A6IK 31/713 (2006.01) Hypertrophic Heart,” Am. J. Pathol. 170(6):183 1-1840 (2007). AOIK 67/027 (2006.01) Kim, “International Search Report,” 4 pages, from International A6IK 38/22 (2006.01) Patent Appl. No. PCT/US2008/071839, Korean Intellectual Property CI2N 9/16 (2006.01) Office, Daejon, Republic of Korea (mailed Jan. 6, 2009). CI2N 15/113 (2010.01) Rooij et al., “A signature pattern of stress-responsive microRNAsthat can evoke cardiac hypertrophy and heart failure,” Proc. Natl. Acad. CI2N 15/85 (2006.01) Sci. USA 103(48):18255-18260 (2006). A6IK 31/7105 (2006.01) Tatsuguchiet al., “Expression of MicroRNAsis Dynamically Regu- A6IK 31/712 (2006.01) lated During Cardiomyocyte Hypertrophy,” J. Mol. Cell. Cardiol. A6IK 31/7125 (2006.01) 42(6):1137-1141 (2007). A61K 39/395 (2006.01) Lagos-Quintanaet al., “New microRNAsfrom mouse and. human,” RNA,vol. 9:175-179, 2003. A6IK 45/06 (2006.01) Lagos-Quintanaet al., “Identification of tissue-specific microRNAs A6IK 31/07 (2006.01) from mouse,” Curent Biology, vol. 12:735-739, 2002. AGIK 31/355 (2006.01) (Continued) A6IK 31/375 (2006.01) (52) US. Cl. Primary Examiner — J. E. Angell CPC oc. A61LK 31/713 (2013.01); AOLK 67/0276 (74) Attorney, Agent, or Firm — Cooley LLP (2013.01); A6LK 38/2242 (2013.01); C12N (57) ABSTRACT 9/16 (2013.01); CI2N 15/113 (2013.01); CI2N The present invention relates to the identification of a 15/8509 (2013.01); AGLK 31/7105 (2013.01); microRNAfamily, designated miR-29a-c, that is a key regu- A61LK 31/712 (2013.01); A6LK 31/7125 lator of fibrosis in cardiac tissue. The inventors show that (2013.01); A6LK 39/3955 (2013.01); A61K members of the miR-29 family are down-regulated in the 45/06 (2013.01); A61K 31/07 (2013.01); A6LK heart tissue in responseto stress, and are up-regulatedin heart 31/355 (2013.01); A6LK 31/375 (2013.01); tissue of mice that are resistant to both stress and fibrosis. AOLK 2207/30 (2013.01); AOLK 2217/052 Also provided are methods of modulating expression and (2013.01); AOLK 2217/075 (2013.01); AOILK activity of the miR-29 family of miRNAsas a treatment for 2217/15 (2013.01); AOLK 2217/206 (2013.01); fibrotic disease, including cardiac hypertrophy, skeletal AOLK 2227/105 (2013.01); AOLK 2267/0375 muscle fibrosis other fibrosis related diseases and collagen (2013.01); CI2N 2310/113 (2013.01); C12N loss-related disease. 2310/141 (2013.01); CI2N 2310/315 (2013.01); 22 Claims, 29 Drawing Sheets US 8,940,711 B2 Page 2 (56) References Cited WO WO2007/081720 A2 7/2007 = WO WO 2007/081740 A2 7/2007 U.S. PATENT DOCUMENTS WO WO 2007/109236 A2 9/2007 WO WO 2007/112754 A2 10/2007 2009/0286969 Al 11/2009 Esauetal. WO WO 2008/016924 A2 2/2008 2009/0291906 Al 11/2009 Esauetal. WO WO 2008/043521 A2 4/2008 2009/0291907 Al 11/2009 Esau et al. WO WO 2008/061537 A2 5/2008 2009/0293148 Al 11/2009 Renetal. 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