Evidence map›Paper›PMID 41129230›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Squamous cell carcinoma antigen-1/SerpinB3 is an endogenous skin injury response element.

Jordan R Yaron, Shubham Pallod, Sepideh Nezhadi, Holly M Gildar, Jayda Hylton-Pelaia, Jordan Roberts, Jacquelyn Kilbourne, Kaushal Rege

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jordan R YaronCenter for Biomaterials Innovation and Translation, The Biodesign Institute, Arizona State University, Tempe, AZ 85281.ORCID 0000-0002-4133-474X
Shubham PallodCenter for Biomaterials Innovation and Translation, The Biodesign Institute, Arizona State University, Tempe, AZ 85281.
Sepideh NezhadiCenter for Biomaterials Innovation and Translation, The Biodesign Institute, Arizona State University, Tempe, AZ 85281.
Holly M GildarCollege of Health Solutions, Arizona State University, Phoenix, AZ 85004.
Jayda Hylton-PelaiaSchool of Life Science, Arizona State University, Tempe, AZ 85287.
Jordan RobertsSchool of Life Science, Arizona State University, Tempe, AZ 85287.
Jacquelyn KilbourneDepartment of Animal Care Technologies, Arizona State University, Tempe, AZ 85281.ORCID 0000-0003-0767-0587
Kaushal RegeCenter for Biomaterials Innovation and Translation, The Biodesign Institute, Arizona State University, Tempe, AZ 85281.

Funding

Bioengineered Skin SealantsR01AR074627 · NIAMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI REGE, KAUSHAL · 2020 to 2023
$1.5M
Inflammasome-modulating Polymeric Biomaterials to Augment Tissue RepairK01EB031984 · NIBIB · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI YARON, JORDAN ROBIN · 2021 to 2023
$303k
ADHS | Arizona Biomedical Research Commission (ABRC) RFGA2022-010-03HHS | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R01AR074627HHS | NIH | National Institute of Biomedical Imaging and Bioengineering (NIBIB) K01EB031984NIAMS NIH HHS R01 AR074627NIBIB NIH HHS K01 EB031984Wound Healing Foundation (WHF) 2022 WHF-3 M Fellowship
6 · The paper itself

Abstract

The squamous cell carcinoma antigen SerpinB3 is a serum-circulating biomarker of epithelial cancers associated with high metastasis, treatment resistance, and poor prognosis. Despite its clinical significance, the endogenous role of SerpinB3 has remained undefined. Here, we identify SerpinB3 as a mediator of epithelial wound healing. Injury induces SerpinB3 expression in vitro and in vivo in the migrating epidermal tongue; overexpression of the protein promotes epithelial-to-mesenchymal transition-like changes. Recombinant Serpinb3a, the mouse ortholog, enhances re-epithelialization in vitro and accelerates wound closure and collagen remodeling in vivo. These findings reveal a physiological function for SerpinB3 in epithelial repair and suggest that its expression in cancer, chronic wounds, and inflammatory diseases may reflect reactivation of a conserved wound response program-positioning SerpinB3 as a compelling therapeutic target.

Indexed as

Antigens, NeoplasmSerpinsSkinWound HealingAnimalsEpithelial-Mesenchymal TransitionHumansMiceAntigens, NeoplasmSerpinssquamous cell carcinoma-related antigenepithelializationepithelial–mesenchymal transitionserpinskin injurywound

Identifiers

PMID41129230
PMCPMC12582253

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.