Cullin 3 as a novel target in diverse pathologies

• Main Authors: Ana Cristina Andérica-Romero, Irma Gabriela González-Herrera, Abel Santamaría, José Pedraza-Chaverri
• Format: Article
• Language: English
• Published: Elsevier 2013-01-01
• Series: Redox Biology
• Subjects: Cullin 3; Proteasome; Nedd8; Nrf2; Oxidative stress; Cell cycle
• Online Access: http://www.sciencedirect.com/science/article/pii/S2213231713000554

Recent evidence suggests that the malfunctioning disposal system of cell protein called ubiquitin–proteasome system (UPS) plays an important role in the development of disorders, including cancer and neurodegenerative diseases. Accumulating evidence suggests that the abnormal regulation of the E3 ubiquitin ligases, essential components of the UPS, contributes to uncontrolled proliferation, genomic instability and cancer, since these ligases and their substrates are involved in the regulation of cell cycle progression, gene transcription, signal transduction, DNA replication and others. Through selective degradation of specific substrates, E3 ligases regulate different biological processes. Cullins are a family of proteins that confer substrate specificity to multimeric complex of E3 ligases acting as scaffold proteins. So far, seven members of the cullin family of proteins have been identified. Interestingly, the data generated by several groups indicate that cullin 3 (Cul3) has begun to emerge as a protein involved in the etiopathology of multiple diseases. In this paper we examine the latest advances in basic research on the biology of Cul3 and how it could help to direct drug discovery efforts on this target.