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Updated: Jun 22, 2026

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Negative growth regulators of the cell cycle machinery and cancer
1Department of Pathophysiology, Sun Yat-Sen University, Guangzhou, PR China.
Abstract:
Cell cycle dysregulation is a critical feature of tumor cells. Numerous cell cycle regulators act either as oncogenes or tumor suppressors and their aberrations result in proliferative advantage for cancer cells. Many molecular targets and their use in either abrogating the growth advantage of oncogenic mediators or enhancing the growth suppressive activity of tumor suppressors, have been filed for patents. The molecular targets associated with cell cycle inhibition are of particular interest because they are potential therapeutic agents of promise in the control of inappropriate cellular proliferation. This review focuses on the recent discovery of potential molecular targets involved in cell cycle inhibition and their evaluation as therapeutic agents for cancers. In this review, the strategies employed to control oncogenesis and their possible clinical applications are discussed.
Insights
Cell cycle regulators are key in cancer. This review highlights novel molecular targets for cell cycle inhibition, offering promising therapeutic strategies to control cancer cell proliferation and oncogenesis.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Cell cycle dysregulation is a hallmark of cancer, with regulators acting as oncogenes or tumor suppressors.
- Aberrant cell cycle control provides a proliferative advantage to tumor cells.
- Numerous molecular targets involved in cell cycle regulation have been patented for therapeutic intervention.
Purpose of the Study:
- To review recent discoveries of molecular targets for cell cycle inhibition.
- To evaluate these targets as potential therapeutic agents for cancer treatment.
- To discuss strategies for controlling oncogenesis and their clinical applications.
Main Methods:
- Literature review of recent scientific publications and patents.
- Focus on molecular targets involved in cell cycle inhibition.
- Analysis of therapeutic potential and clinical applications.
Main Results:
- Identification of novel molecular targets critical for cell cycle control.
- Evaluation of these targets for their efficacy in inhibiting cancer cell proliferation.
- Discussion of patented strategies for targeting cell cycle regulators.
Conclusions:
- Molecular targets involved in cell cycle inhibition represent promising therapeutic agents.
- Targeting cell cycle dysregulation offers a viable strategy for cancer treatment.
- Further research and clinical evaluation are warranted for these potential cancer therapies.
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