Evidence map›Paper›PMID 41876478›Full record

ReviewCell death discovery2026

p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials.

Yujia Cong, Zhenglin He, Hanming Hao, Haoran Chen, Anqi Chen, Chunyi Li, Yue Hu, Xianling Cong

Abstract readReview
In one paragraph

Review in Cell death discovery, 2026. 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.

Yujia CongChina-Japan Union Hospital of Jilin University, Jilin University, Changchun, China.
Zhenglin HeChina-Japan Union Hospital of Jilin University, Jilin University, Changchun, China. lioushe@126.com.ORCID http://orcid.org/0009-0004-9708-0605
Hanming HaoCollege of Basic Medical Sciences, Jilin University, Changchun, China.
Haoran ChenChina-Japan Union Hospital of Jilin University, Jilin University, Changchun, China.
Anqi ChenChina-Japan Union Hospital of Jilin University, Jilin University, Changchun, China.
Chunyi LiInstitute of Antler Science and Product Technology, Changchun Sci-Tech University, Changchun, China.ORCID http://orcid.org/0000-0001-7275-4440
Yue HuChina-Japan Union Hospital of Jilin University, Jilin University, Changchun, China. yuehu@jlu.edu.cn.
Xianling CongChina-Japan Union Hospital of Jilin University, Jilin University, Changchun, China. congxl@jlu.edu.cn.ORCID http://orcid.org/0000-0002-5790-4188

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a pivotal member of the p53 family, the p63 gene plays an indispensable role in skin homeostasis and development. The gene encodes multiple isoforms, primarily TAp63 and ΔNp63, which differentially regulate cell proliferation, differentiation, and stress responses through complementary mechanisms. This comprehensive review systematically examines the molecular mechanisms and cellular functions of p63 in cutaneous biology, with particular emphasis on its dual roles in maintaining skin integrity and contributing to disease pathogenesis. We detail the essential functions of p63 in skin development, encompassing epithelial fate determination, chromatin remodeling, cell adhesion, and barrier formation, while also exploring its involvement in skin regeneration and differentiation via metabolic reprogramming and stem cell modulation. Furthermore, we analyze how mutations in p63 underlie ectodermal dysplasia and various dermatological disorders, underscoring the gene's fundamental importance in cutaneous health. By integrating current knowledge of the diverse biological roles of p63 and its associated therapeutic potential as a target, this review highlights its central significance in both skin physiology and pathology.

Identifiers

PMID41876478
PMCPMC13039162

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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 OpenQuestion graph.