Cyclin E

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Cyclin Expression.svg

Cyclin E is a member of the cyclin family of proteins, which play a critical role in regulating the cell cycle. Cyclin E, in particular, is essential for the transition from the G1 phase to the S phase of the cell cycle, a process that is crucial for DNA replication and cell division. The activity of cyclin E is primarily regulated through its association with cyclin-dependent kinase 2 (CDK2), forming a complex that is necessary for the progression of the cell cycle.

Function[edit | edit source]

Cyclin E binds to CDK2 in the late G1 phase, activating the kinase activity of CDK2. This activation leads to the phosphorylation of several target proteins that are essential for DNA replication and the initiation of the S phase. The cyclin E-CDK2 complex thus plays a pivotal role in ensuring that cells are ready to enter the S phase, with all the necessary preparations for DNA synthesis being completed.

Regulation[edit | edit source]

The expression and activity of cyclin E are tightly regulated at multiple levels, including transcriptional, post-transcriptional, and post-translational modifications. Cyclin E levels are low in the early G1 phase and start to increase as the cell progresses towards the S phase. After its peak in the G1-S transition, cyclin E is degraded via the ubiquitin-proteasome pathway, ensuring that its activity is transient and tightly controlled.

Clinical Significance[edit | edit source]

Abnormalities in cyclin E expression and function have been implicated in the pathogenesis of various cancers. Overexpression of cyclin E can lead to uncontrolled cell proliferation, a hallmark of cancer. In particular, high levels of cyclin E have been observed in breast cancer, ovarian cancer, and colorectal cancer, among others. As such, cyclin E is considered a potential biomarker for cancer diagnosis and prognosis, as well as a target for therapeutic intervention.

Research[edit | edit source]

Research on cyclin E has focused on understanding its role in cell cycle regulation, its mechanisms of action, and its involvement in cancer. Studies have also explored the potential of targeting cyclin E in cancer therapy, either by inhibiting its activity or by modulating its expression levels. Additionally, research is being conducted to identify biomarkers associated with cyclin E overexpression in cancer, which could aid in early detection and treatment.


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Contributors: Prab R. Tumpati, MD