The invention provides application of an NCOA3 polyQ structural domain in preparation of a
medicine for relieving ocular vascular abnormal
hyperplasia diseases, relates to the technical field of
biomedicine, and aims to solve the problems that in the prior art, an ocular
pathological angiogenesis mechanism is complex, and safe and effective targeted intervention means are lacked. The construction of a mouse corneal micropocket
pathological angiogenesis model proves that Nco3polyQ structural domain deletion can significantly inhibit
corneal neovascularization: compared with a WT mouse, the Nco3wt / Q mouse corneal tissue CD31 positive
signal is reduced, the number of
corneal neovascularization in the Nco3Q / Q mouse is minimum, and the CD31 positive area is minimum; meanwhile, qPCR (quantitative
polymerase chain reaction) detection of corneal tissues shows that mRNA (
messenger ribonucleic acid) expression of the vascular marker genes Pecam1 and Cdh5 is in a decreasing trend and is further decreased in an Nco3Q / Q mouse. On the basis, the intervention strategy aiming at the NCOA3 polyQ structural domain is used for preparing the
medicine for relieving the abnormal
hyperplasia diseases of the ocular blood vessels, and a new
treatment strategy and a potential target are provided for related diseases of the
ophthalmology department.