Skip to content
Open access · OA via OpenAlex

MiR-34, SIRT1, and p53: The feedback loop

Munekazu Yamakuchi, Charles J. Lowenstein

Cell Cycle · 2009 · ▲ 468 citations

Abstract

MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression. Several studies have linked dysregulation of miRNA with tumorigenesis. The TP53 is one of the most commonly mutated genes in human cancers, and its gene product p53 activates transcription of a set of miRNA including the miR-34 family of miRNA. The miR-34 family regulates cell cycle progression, cellular senescence(definition) and apoptosis, but the targets of miR-34 are not completely defined. We recently found that miR-34a inhibits SIRT1, a gene that regulates cellular senescence and limits longevity. SIRT1 also regulates p53 dependent apoptosis through deacetylating and stabilizing p53. We also discovered that SIRT1 mediates miR-34a activation of apoptosis by regulating p53 activity. Based on this observation, we propose a positive feedback loop, in which p53 induces expression of miR-34a which suppresses SIRT1, increasing p53 activity.

◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:

Read at source →

Provenance

Source
OpenAlex
DOI
10.4161/cc.8.5.7753
Canonical
link ↗
Fetched
2026-10-23 MST

Cite this

APA
Yamakuchi, M., &amp; Lowenstein, C.J. (2009). MiR-34, SIRT1, and p53: The feedback loop. <em>Cell Cycle</em>. https://doi.org/10.4161/cc.8.5.7753
Vancouver
Yamakuchi M, Lowenstein CJ. MiR-34, SIRT1, and p53: The feedback loop. Cell Cycle. 2009. doi:10.4161/cc.8.5.7753.
BibTeX
@article{munekazu2009MiRSIR, title = {MiR-34, SIRT1, and p53: The feedback loop}, author = {Munekazu Yamakuchi and Charles J. Lowenstein}, journal = {Cell Cycle}, year = {2009}, doi = {10.4161/cc.8.5.7753}, }

Research neighborhood

References, citing works, and semantically nearest findings. Click a node to open it.

Related findings