Related Experiment Video
Updated: Jan 29, 2026

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
Epigenetic Regulation of iASPP-p63 Feedback Loop in Cutaneous Squamous Cell Carcinoma
Deborah J Robinson1, Ankit Patel1, Karin J Purdie1
1Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary London University, London, UK.
Abstract:
Keratinocyte skin cancer, comprising cutaneous squamous (cSCC) and basal cell carcinoma, is the most common malignancy in the United Kingdom. P53 is frequently mutated in cSCC. iASPP is a key inhibitor of p53 and NF-κB signaling pathways and has been documented as highly expressed in several types of human cancer. We have previously identified an autoregulatory feedback loop between iASPP and p63, which is critical in epidermal homeostasis. We hypothesized a potential role for dysregulation of this axis in the pathogenesis of keratinocyte malignancies. Immunostaining of 116 cSCC clinical samples revealed increased iASPP and ΔNp63 expression, but also highlighted a significant alteration of iASPP cellular localization, with consequent deregulation of its function. Expression patterns, functionality, and gene and microRNA expression analysis were further investigated in 10 cSCC cell lines. Our data suggest that while direct effects of iASPP and p63 upon each other's expression are maintained in cSCC, epigenetic dysregulation of the feedback loop occurs at the microRNA level by a previously unreported mechanism controlling p63 expression. We demonstrate that this autoregulatory feedback loop controls cell migration in cSCC by blocking epithelial-mesenchymal transition and promoting proliferation, and provides future directions for clinical biomarker and therapeutic target discovery in cutaneous SCC.
Insights
Dysregulation of the iASPP-p63 feedback loop, involving microRNA epigenetic changes, drives keratinocyte skin cancer (cSCC) by altering cell migration and proliferation. This axis offers potential therapeutic targets for cSCC.
Area of Science:
- Oncology
- Dermatology
- Molecular Biology
Background:
- Cutaneous squamous cell carcinoma (cSCC) is a common skin cancer.
- iASPP is an inhibitor of p53 and NF-κB pathways, often overexpressed in cancers.
- An autoregulatory feedback loop between iASPP and p63 is crucial for skin homeostasis.
Purpose of the Study:
- To investigate the role of the iASPP-p63 axis in keratinocyte malignancies.
- To explore potential epigenetic dysregulation of this feedback loop in cSCC.
- To identify iASPP and p63 as potential biomarkers and therapeutic targets for cSCC.
Main Methods:
- Immunostaining of 116 cSCC clinical samples.
- Expression, functionality, and gene/microRNA analysis in 10 cSCC cell lines.
- Assessment of the iASPP-p63 feedback loop's role in cell migration and epithelial-mesenchymal transition (EMT).
Main Results:
- Increased iASPP and ΔNp63 expression observed in cSCC samples.
- Alterations in iASPP cellular localization and function were noted.
- Epigenetic dysregulation at the microRNA level impacts p63 expression, affecting the feedback loop.
Conclusions:
- The iASPP-p63 autoregulatory feedback loop is dysregulated in cSCC, partly via microRNA mechanisms.
- This dysregulation impacts cell migration by influencing EMT and proliferation.
- The iASPP-p63 axis presents a promising avenue for cSCC biomarker and therapeutic development.
Related Concept Videos
Epigenetic Regulation
Epigenetic Regulation
X-chromosome...
Feedback Loops
Cell Signaling Feedback Loops
Negative feedback loops
Most signaling systems have negative feedback loops that can perform different functions such as output limiter, and adaptation.
Output limiter
Upon receiving an input signal, the cellular response rapidly increases until a threshold is reached. Beyond this threshold, a negative feedback loop...
Positive and Negative Feedback Loops
Feedback Regulation of Calcium Concentration
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...

