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Functional genomics of PCOS: from GWAS to molecular mechanisms.
McAllister, Jan M; Legro, Richard S; Modi, Bhavi P; Strauss, Jerome F.
Afiliação
  • McAllister JM; Department of Pathology, Penn State Hershey College of Medicine, Hershey, PA, USA; Department of Obstetrics and Gynecology, Penn State Hershey College of Medicine, Hershey, PA, USA. Electronic address: jmcallister@psu.edu.
  • Legro RS; Department of Obstetrics and Gynecology, Penn State Hershey College of Medicine, Hershey, PA, USA.
  • Modi BP; Department of Obstetrics and Gynecology, Virginia Commonwealth University, Richmond, VA, USA.
  • Strauss JF; Department of Obstetrics and Gynecology, Virginia Commonwealth University, Richmond, VA, USA.
Trends Endocrinol Metab ; 26(3): 118-24, 2015 Mar.
Article em En | MEDLINE | ID: mdl-25600292
Polycystic ovary syndrome (PCOS) is a common endocrinopathy characterized by increased ovarian androgen biosynthesis, anovulation, and infertility. PCOS has a strong heritable component based on familial clustering and twin studies. Genome-wide association studies (GWAS) identified several PCOS candidate loci including LHCGR, FSHR, ZNF217, YAP1, INSR, RAB5B, and C9orf3. We review the functional roles of strong PCOS candidate loci focusing on FSHR, LHCGR, INSR, and DENND1A. We propose that these candidates comprise a hierarchical signaling network by which DENND1A, LHCGR, INSR, RAB5B, adapter proteins, and associated downstream signaling cascades converge to regulate theca cell androgen biosynthesis. Future elucidation of the functional gene networks predicted by the PCOS GWAS will result in new diagnostic and therapeutic approaches for women with PCOS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Ovário Policístico / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Loci Gênicos Limite: Female / Humans Idioma: En Revista: Trends Endocrinol Metab Assunto da revista: ENDOCRINOLOGIA / METABOLISMO Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Ovário Policístico / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Loci Gênicos Limite: Female / Humans Idioma: En Revista: Trends Endocrinol Metab Assunto da revista: ENDOCRINOLOGIA / METABOLISMO Ano de publicação: 2015 Tipo de documento: Article