Related Experiment Video
Updated: Jul 9, 2026

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
The guardian's little helper: microRNAs in the p53 tumor suppressor network
Xingyue He1, Lin He, Gregory J Hannon
1Watson School of Biological Sciences, Howard Hughes Medical Institute, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, NY 11724, USA.
Abstract:
Several microRNAs (miRNAs) have been implicated in tumor development based on both changes in their expression patterns and gene structural alterations in human tumors. However, we are only now beginning to see how miRNAs interact with classic oncogene and tumor suppressor mechanisms. Several recent studies have implicated the miR-34 family of miRNAs in the p53 tumor suppressor network. The expression of miR-34a, miR-34b, and miR-34c is robustly induced by DNA damage and oncogenic stress in a p53-dependent manner. When overexpressed, miR-34 leads to apoptosis or cellular senescence, whereas reduction of miR-34 function attenuates p53-mediated cell death. These findings, together with the fact that miR-34 is down-regulated in several types of human cancer, show that miRNAs can affect tumorigenesis by working within the confines of well-known tumor suppressor pathways.
Insights
The miR-34 family of microRNAs (miRNAs) acts as tumor suppressors by interacting with the p53 pathway. Reduced miR-34 expression in cancers highlights its role in tumorigenesis.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- MicroRNAs (miRNAs) are increasingly recognized for their roles in cancer development.
- Their interaction with established tumor suppressor pathways, like p53, is an emerging area of research.
Purpose of the Study:
- To investigate the role of the miR-34 family in the p53 tumor suppressor network.
- To understand how miR-34 functions contribute to or prevent tumorigenesis.
Main Methods:
- Analysis of miR-34 family expression patterns in human tumors.
- Investigating the p53-dependent induction of miR-34a, miR-34b, and miR-34c by DNA damage and oncogenic stress.
- Assessing the functional consequences of miR-34 overexpression and reduced function on cell death pathways.
Main Results:
- The expression of miR-34a, miR-34b, and miR-34c is induced by DNA damage and oncogenic stress in a p53-dependent manner.
- Overexpression of miR-34 induces apoptosis or cellular senescence.
- Reduced miR-34 function impairs p53-mediated cell death.
Conclusions:
- The miR-34 family functions as a critical component of the p53 tumor suppressor pathway.
- Down-regulation of miR-34 in human cancers suggests its role in tumorigenesis.
- miRNAs can influence cancer development by modulating well-known tumor suppressor mechanisms.
Related Concept Videos
Abnormal Proliferation
Negative Regulator Molecules
MicroRNAs
MicroRNAs
MicroRNAs
mTOR Signaling and Cancer Progression
The mTOR pathway or the...