Related Experiment Video
Updated: May 24, 2026

Induction and Validation of Cellular Senescence in Primary Human Cells
Published on: June 20, 2018
Tristetraprolin: roles in cancer and senescence
Christina R Ross1, Sarah E Brennan-Laun, Gerald M Wilson
1Department of Biochemistry and Molecular Biology and Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Abstract:
Cancer and senescence are both complex transformative processes that dramatically alter many features of cell physiology and their interactions with surrounding tissues. Developing the wide range of cellular features characteristic of these conditions requires profound alterations in global gene expression patterns, which can be achieved by suppressing, activating, or uncoupling cellular gene regulatory pathways. Many genes associated with the initiation and development of tumors are regulated at the level of mRNA decay, frequently through the activity of AU-rich mRNA-destabilizing elements (AREs) located in their 3'-untranslated regions. As such, cellular factors that recognize and control the decay of ARE-containing mRNAs can influence tumorigenic or senescent phenotypes mediated by products of these transcripts. In this review, we discuss evidence showing how suppressed expression and/or activity of the ARE-binding protein tristetraprolin (TTP) can contribute to these processes. Next, we outline current findings linking TTP suppression to exacerbation of individual tumorigenic phenotypes, and the roles of specific TTP substrate mRNAs in mediating these effects. Finally, we survey potential mechanisms that cells may employ to suppress TTP expression in cancer, and propose potential diagnostic and therapeutic strategies that may exploit the relationship between TTP expression and tumor progression or senescence.
Insights
Tristetraprolin (TTP) protein suppression contributes to cancer and senescence by altering gene expression. Understanding TTP
Area of Science:
- Molecular Biology
- Cell Biology
- Cancer Research
Background:
- Cancer and senescence involve significant cellular and tissue alterations driven by gene expression changes.
- mRNA decay, regulated by AU-rich elements (AREs), influences genes critical for tumor initiation and development.
- ARE-binding proteins control mRNA decay, impacting tumorigenic and senescent phenotypes.
Purpose of the Study:
- To review the role of tristetraprolin (TTP) in cancer and senescence.
- To examine how suppressed TTP expression contributes to tumorigenic phenotypes.
- To explore mechanisms of TTP suppression and potential therapeutic strategies.
Main Methods:
- Review of existing scientific literature on TTP, mRNA decay, cancer, and senescence.
- Analysis of evidence linking TTP activity to gene regulation in cellular transformation.
- Survey of proposed mechanisms for TTP suppression in cancer cells.
Main Results:
- Suppressed expression or activity of TTP is linked to the development of cancer and senescence.
- Specific TTP target mRNAs play a role in mediating tumorigenic phenotypes when TTP is suppressed.
- Evidence suggests various cellular mechanisms can lead to reduced TTP expression in cancer.
Conclusions:
- Reduced TTP levels can promote cancer progression and senescence.
- Targeting TTP expression may offer novel diagnostic and therapeutic avenues for cancer.
- Further research into TTP regulation and its substrates is crucial for understanding tumor development.
Related Concept Videos
Replicative Cell Senescence
Replicative Cell Senescence
Negative Regulator Molecules
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
Cancer-Critical Genes II: Tumor Suppressor Genes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
Cancer-Critical Genes II: Tumor Suppressor Genes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...

