The Biology of Retinoblastoma.

Abstract

Retinoblastoma, the most common primary intraocular cancer of childhood, is a malignancy arising in the developing retina. Tumor formation usually begins with mutation in both alleles of the retinoblastoma tumor suppressor gene RB1, followed by a series of other genetic alterations that correlate with the clinical stage and pathologic findings of the tumor. Analysis of sporadic and heritable retinoblastoma led to the development of Knudson's Two-Hit Hypothesis. The tumor suppressor RB1 gene codes for the retinoblastoma protein which is a key regulator of cellular replication via its binding to the E2F family of transcription factors and chromatin remodeling proteins. Studies of preclinical models of retinoblastoma in the form of transgenic mice and xenograft animal models have significantly contributed to the development of effective therapies for this disease. Research on retinoblastoma has paved the way toward understanding many of the mechanisms in cancer genetics.

• Authors: Pia R Mendoza, Hans E Grossniklaus
• Journal: Progress in molecular biology and translational science (Prog Mol Biol Transl Sci) Vol. 134 Pg. 503-16 ( 2015) ISSN: 1878-0814 [Electronic] Netherlands
• PMID: 26310174 (Publication Type: Journal Article, Review)
• Copyright: © 2015 Elsevier Inc. All rights reserved.

Chemical References

• Retinoblastoma Protein

Topics

• Animals
• Disease Progression
• Genetic Predisposition to Disease
• Humans
• Retinoblastoma (genetics, pathology, therapy)
• Retinoblastoma Protein (genetics)