TY - JOUR
T1 - Chemical genomics identifies compounds affecting Xenopus laevis pigment cell development
AU - Tomlinson, M.L.
AU - Rejzek, M.
AU - Fidock, M.
AU - Field, R.A.
AU - Wheeler, G.N.
PY - 2009
Y1 - 2009
N2 - A forward chemical genomic screen was carried out using Xenopus laevis embryos to identify compounds disrupting pigmented cell development, including the retinal pigment epithelial (RPE) layer of the eye and the melanophores (melanocytes). Phenotypes showing changes in cell migration, morphology and pigmentation were observed. The screen also identified compounds affecting other aspects of Xenopus development including general patterning and morphogenesis, eye development and edema formation. Evidence is presented for the molecular targets of three of the compounds identified. Xenopus melanophore and human melanoma cell lines were also utilised in follow-up cell morphology assays. Chemical genomic screens of this type have an important role to play in the identification of novel compounds providing new molecular tools, and biological information, along with identification of new protein targets and leads for potential therapeutic agents. © The Royal Society of Chemistry 2009.
AB - A forward chemical genomic screen was carried out using Xenopus laevis embryos to identify compounds disrupting pigmented cell development, including the retinal pigment epithelial (RPE) layer of the eye and the melanophores (melanocytes). Phenotypes showing changes in cell migration, morphology and pigmentation were observed. The screen also identified compounds affecting other aspects of Xenopus development including general patterning and morphogenesis, eye development and edema formation. Evidence is presented for the molecular targets of three of the compounds identified. Xenopus melanophore and human melanoma cell lines were also utilised in follow-up cell morphology assays. Chemical genomic screens of this type have an important role to play in the identification of novel compounds providing new molecular tools, and biological information, along with identification of new protein targets and leads for potential therapeutic agents. © The Royal Society of Chemistry 2009.
UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-62949098600&partnerID=MN8TOARS
UR - https://www.scopus.com/pages/publications/62949098600
U2 - 10.1039/b818695b
DO - 10.1039/b818695b
M3 - Article
SN - 1742-206X
SP - 376
EP - 384
JO - Molecular BioSystems
JF - Molecular BioSystems
ER -