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Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
The expanding regulatory universe of p53 in gastrointestinal cancer
Andrew Fesler1, Ning Zhang2, Jingfang Ju1
1Translational Research Laboratory, Department of Pathology, Stony Brook University, Stony Brook, USA.
Abstract:
Tumor suppresser gene TP53 is one of the most frequently deleted or mutated genes in gastrointestinal cancers. As a transcription factor, p53 regulates a number of important protein coding genes to control cell cycle, cell death, DNA damage/repair, stemness, differentiation and other key cellular functions. In addition, p53 is also able to activate the expression of a number of small non-coding microRNAs (miRNAs) through direct binding to the promoter region of these miRNAs. Many miRNAs have been identified to be potential tumor suppressors by regulating key effecter target mRNAs. Our understanding of the regulatory network of p53 has recently expanded to include long non-coding RNAs (lncRNAs). Like miRNA, lncRNAs have been found to play important roles in cancer biology. With our increased understanding of the important functions of these non-coding RNAs and their relationship with p53, we are gaining exciting new insights into the biology and function of cells in response to various growth environment changes. In this review we summarize the current understanding of the ever expanding involvement of non-coding RNAs in the p53 regulatory network and its implications for our understanding of gastrointestinal cancer.
Insights
The tumor suppressor gene TP53 interacts with non-coding RNAs, including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs). This interaction is crucial for understanding gastrointestinal cancer biology and developing new therapeutic strategies.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- The TP53 gene, a critical tumor suppressor, is frequently altered in gastrointestinal cancers.
- p53 functions as a transcription factor, regulating genes involved in cell cycle, apoptosis, and DNA repair.
- p53 also influences non-coding RNAs, such as microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), which are implicated in cancer.
Purpose of the Study:
- To review the current understanding of non-coding RNAs within the p53 regulatory network.
- To explore the implications of these non-coding RNAs in gastrointestinal cancer biology.
Main Methods:
- Literature review of studies on TP53, miRNAs, lncRNAs, and gastrointestinal cancer.
- Analysis of the regulatory interactions between p53 and non-coding RNAs.
- Synthesis of current knowledge on the role of non-coding RNAs in p53-mediated cancer pathways.
Main Results:
- p53 directly regulates the expression of numerous miRNAs and interacts with lncRNAs.
- Both miRNAs and lncRNAs function as tumor suppressors or oncogenes by targeting mRNAs.
- The interplay between p53 and non-coding RNAs significantly impacts cellular functions and cancer development.
Conclusions:
- Non-coding RNAs are integral components of the p53 regulatory network.
- Understanding these interactions provides novel insights into gastrointestinal cancer pathogenesis.
- Targeting the p53-non-coding RNA axis holds potential for future cancer therapies.
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