Pharmacological Inhibition of a MicroRNA Family in Nonhuman Primates by a Seed-Targeting 8-Mer AntimiR

Author:

Rottiers Veerle12,Obad Susanna3,Petri Andreas34,McGarrah Robert567,Lindholm Marie W.3,Black Joshua C.18,Sinha Sumita56,Goody Robin J.9,Lawrence Matthew S.9,deLemos Andrew S.10,Hansen Henrik F.3,Whittaker Steve9,Henry Steve9,Brookes Rohn9,Najafi-Shoushtari Seyed Hani1211,Chung Raymond T.10,Whetstine Johnathan R.18,Gerszten Robert E.56,Kauppinen Sakari34,Näär Anders M.12

Affiliation:

1. Massachusetts General Hospital Cancer Center, Charlestown, MA 02129, USA.

2. Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

3. Santaris Pharma, DK-2970 Hørsholm, Denmark.

4. Department of Haematology, Aalborg University Hospital, DK-2450 Copenhagen SV, Denmark.

5. Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Boston, MA 02114, USA.

6. Cardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

7. Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.

8. Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.

9. RxGen Inc., 100 Deepwood Drive, Hamden, CT 06517, USA.

10. Gastrointestinal Unit, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

11. Department of Cell and Developmental Biology, Weill Cornell Medical College in Qatar, Education City, Qatar Foundation, P. O. Box 24144, Doha, Qatar.

Abstract

Long-term treatment of obese, insulin-resistant nonhuman primates with a seed-targeting antimiR oligonucleotide against the microRNA-33 family derepresses hepatic expression of miR-33 targets, increases circulating HDL cholesterol, and has a clean safety profile.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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