Gene research progress of retinoblastoma

Authors: Yu Tian,  Chen Changzheng,  Xing Yiqiao

DOI: 10.3760/cma.j.issn.2095-0160.2017.08.019
Published 2017-08-10
Cite as Chin J Exp Ophthalmol, 2017,35(8): 756-760.

Abstract                               [Download PDF] [Read Full Text]

Retinoblastoma (RB) is a common intraocular malignant tumor of infants.It not only seriously threats children’s eyesight, but also endangers their lives.RB develops from the immature cells of retina and its occurrence is closely related with the tumor suppressor gene RB1.The inactivation of two alleles of RB1 is the basis of RB occurrence and development.With the rapid development of biological technology, RB gene related research has made great progress.Researches showed that there are many changes in the chromosome level of RB.Many genes are also involved in the development and progression of RB, including oncogene MYCN, murine double minute 4 (MDM4, also known as MDMX), driver protein family members 14 (KIF14), DEK, E2F3, tumor suppressor gene calcium 11 (CDH11) and so on.This review summarizes the progress in gene research of RB, reveal pathogenesis of RB on DNA molecular level and provides a scientific basis for clinical doctors to formulate effective therapeutic plans.

Key words:

Retinoblastoma; RB1MYCN; Gene

Contributor Information

Yu Tian
Department of Ophthalmology, Renmin Hospital of Wuhan University, Wuhan 430060, China
Chen Changzheng
Xing Yiqiao
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Updated: February 20, 2023 — 1:45 am