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Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
MicroRNA Control of p53
Juan Liu1, Cen Zhang1, Yuhan Zhao1
1Department of Radiation Oncology, Rutgers Cancer Institute of New Jersey, Rutgers, State University of New Jersey, New Brunswick 08903, New Jersey.
Abstract:
Tumor suppressor p53 plays a central role in tumor suppression. As a transcription factor, p53 mainly exerts its tumor suppressive function through transcriptional regulation of many target genes. To maintain the proper function of p53, p53 protein level and activity are exquisitely controlled by a group of positive and negative regulators in cells. Thus, p53, its regulators, and regulated genes form a complicated p53 signaling network. microRNAs (miRNAs) are a group of endogenous small non-coding RNA molecules. miRNAs play an important role in regulation of gene expression by blocking translational protein synthesis and/or degrading target mRNAs. Recent studies have demonstrated that p53 and its network are regulated by miRNAs at multiple levels. Some miRNAs regulate the level and function of p53 through directly targeting p53, whereas some other miRNAs target regulators of p53, such as MDM2 and MDM4, to indirectly regulate the activity and function of p53. On the other hand, p53 also regulates the transcriptional expression and the biogenesis of a group of miRNAs, which contributes to the tumor suppressive function of p53. p53 is the most frequently mutated gene in human cancer. Many tumor-associated mutant p53, which have "gain-of-function" activities in tumorigenesis independently of wild type p53, can regulate the expression of different miRNAs and modulate the biogenesis of specific miRNAs to promote tumorigenesis. These findings have demonstrated that miRNAs are important regulators and mediators of p53 and its signaling pathway, which highlights a pivotal role of miRNAs in the p53 network and cancer. J. Cell. Biochem. 118: 7-14, 2017. © 2016 Wiley Periodicals, Inc.
Insights
MicroRNAs (miRNAs) regulate the p53 signaling network at multiple levels. Both wild-type and mutant p53 interact with miRNAs, influencing gene expression and impacting cancer development.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- The tumor suppressor p53 is crucial for preventing cancer, functioning as a transcription factor that regulates target genes.
- p53's activity is tightly controlled by a complex network of regulators, forming the p53 signaling pathway.
- microRNAs (miRNAs) are small non-coding RNAs that regulate gene expression post-transcriptionally.
Purpose of the Study:
- To explore the intricate relationship between miRNAs and the p53 signaling network.
- To elucidate how miRNAs modulate p53 levels, activity, and its regulatory network.
- To understand the role of miRNAs in both normal p53 function and cancer-associated mutant p53 activity.
Main Methods:
- Review of recent studies investigating miRNA interactions with p53 and its regulators.
- Analysis of how miRNAs directly target p53 or its key regulators (e.g., MDM2, MDM4).
- Examination of p53's role in regulating miRNA expression and biogenesis.
Main Results:
- miRNAs regulate p53 network components at multiple levels, affecting p53 protein levels and function.
- p53 directly and indirectly influences miRNA expression and biogenesis, contributing to tumor suppression.
- Tumor-associated mutant p53 can alter miRNA expression to promote tumorigenesis.
Conclusions:
- miRNAs are critical regulators and mediators within the p53 signaling network.
- The interplay between p53 and miRNAs is pivotal in cancer development and progression.
- Targeting miRNA-p53 interactions presents potential therapeutic strategies for cancer.
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