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Aptamers as Therapeutics.
Nimjee, Shahid M; White, Rebekah R; Becker, Richard C; Sullenger, Bruce A.
Afiliação
  • Nimjee SM; Department of Neurological Surgery, The Ohio State University Wexner Medical Center, Columbus, Ohio 43210; email: shahid.nimjee@osumc.edu.
  • White RR; Department of Surgery, Duke University Medical Center, Durham, North Carolina 27705; email: rebekah.white@duke.edu.
  • Becker RC; Department of Medicine, University of Cincinnati Medical Center, Cincinnati, Ohio 45267; email: beckerrc@ucmail.uc.edu.
  • Sullenger BA; Department of Surgery, Duke University Medical Center, Durham, North Carolina 27705; email: rebekah.white@duke.edu.
Annu Rev Pharmacol Toxicol ; 57: 61-79, 2017 01 06.
Article em En | MEDLINE | ID: mdl-28061688
ABSTRACT
Aptamers are single-stranded nucleic acid molecules that bind to and inhibit proteins and are commonly produced by systematic evolution of ligands by exponential enrichment (SELEX). Aptamers undergo extensive pharmacological revision, which alters affinity, specificity, and therapeutic half-life, tailoring each drug for a specific clinical need. The first therapeutic aptamer was described 25 years ago. Thus far, one aptamer has been approved for clinical use, and numerous others are in preclinical or clinical development. This review presents a short history of aptamers and SELEX, describes their pharmacological development and optimization, and reviews potential treatment of diseases including visual disorders, thrombosis, and cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aptâmeros de Nucleotídeos / Técnica de Seleção de Aptâmeros Tipo de estudo: Clinical_trials Limite: Animals / Humans Idioma: En Revista: Annu Rev Pharmacol Toxicol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aptâmeros de Nucleotídeos / Técnica de Seleção de Aptâmeros Tipo de estudo: Clinical_trials Limite: Animals / Humans Idioma: En Revista: Annu Rev Pharmacol Toxicol Ano de publicação: 2017 Tipo de documento: Article