Small molecules targeting glycogen synthase kinase 3 as potential drug candidates for the treatment of retinitis pigmentosa Articles uri icon

authors

  • MARCHENA, MIGUEL
  • VILLAREJO-ZORI, BEATRIZ
  • ZALDIVAR DIEZ DE BONILLA, JOSEFA
  • PALOMO, VALLE
  • GIL, CARMEN
  • HERNÁNDEZ-SÁNCHEZ, CATALINA
  • MARTINEZ FINKELSHTEIN, ANDREI
  • MARTÍNEZ, ANA
  • DE LA ROSA, ENRIQUE J.

publication date

  • January 2017

start page

  • 522

end page

  • 526

issue

  • 1

volume

  • 32

International Standard Serial Number (ISSN)

  • 1475-6366

Electronic International Standard Serial Number (EISSN)

  • 1475-6374

abstract

  • Retinitis pigmentosa (RP) is an inherited retinal dystrophy that courses with progressive degeneration of retinal tissue and loss of vision. Currently, RP is an unpreventable, incurable condition. We propose glycogen synthase kinase 3 (GSK-3) inhibitors as potential leads for retinal cell neuroprotection, since the retina is also a part of the central nervous system and GSK-3 inhibitors are potent neuroprotectant agents. Using a chemical genetic approach, diverse small molecules with different potency and binding mode to GSK-3 have been used to validate and confirm GSK-3 as a pharmacological target for RP. Moreover, this medicinal chemistry approach has provided new leads for the future disease-modifying treatment of RP.

subjects

  • Biology and Biomedicine
  • Pharmacy

keywords

  • gsk-3 inhibitors; retinal diseases; retinitis pigmentosa; glaucoma