Evidence map›Paper›PMID 42064974›Full record

ArticleJID innovations : skin science from molecules to population health2026

The human Flower isoform hFWE4 facilitates cornification in cutaneous squamous cell carcinoma.

Justin C Rudd, Patrick T Kuwong, Rachel E Johnson, Louise N Monga-Wells, Meghan Vo, Julia Russolillo, Shreya Reddy, Mallory Jacob, Hunter Litz, Changzhao Li and 3 more

Abstract read
In one paragraph

Article in JID innovations : skin science from molecules to population health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

13 authors.

Justin C RuddDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Patrick T KuwongDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Rachel E JohnsonDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Louise N Monga-WellsDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Meghan VoDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Julia RussolilloDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Shreya ReddyDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Mallory JacobDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Hunter LitzDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Changzhao LiDepartment of Pathology, Creighton University School of Medicine, Omaha, Nebraska, USA.
Andrew SirefDepartment of Pathology, Creighton University School of Medicine, Omaha, Nebraska, USA.
James A GrunkemeyerDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.
Laura A HansenDepartment of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arising from epidermal keratinocytes, cutaneous squamous cell carcinoma (cSCC) is the second most common human tumor. Transformed keratinocytes in cSCC retain partial ability to execute terminal-differentiation, forming keratinized, cyst-like structures called 'keratin pearls' rather than normal stratified epidermis. It is readily appreciated that well-differentiated tumors have better prognosis than poorly differentiated ones; however, molecular mechanisms governing terminal differentiation in cSCC remain incompletely understood. Delineating these mechanisms promises to identify additional differentiation-associated molecules that could serve as histologic markers for prognostic stratification. In this study, we demonstrate that FWE (Flower), a newly described regulator of lamellar body trafficking in normal epidermis, is specifically expressed in highly differentiated cSCC layers. Genetic knockout of FWE dysregulates cornification and lamellar body-related gene expression, causing abnormal keratinization, whereas ectopic hFWE4 expression drives G1 arrest and exit from the proliferative basal keratinocyte population. Poorly differentiated human cSCC exhibit minimal FWE positivity, whereas well-differentiated regions show readily detectable FWE. We propose that, as in normal epidermis, FWE facilitates late stages of cornification in cSCC and represents a differentiation marker that can classify differentiation status to improve prognostic stratification of these tumors.

Indexed as

CornificationcSCCDifferentiationKeratinocyte

Identifiers

PMID42064974
PMCPMC13125993

What OpenQuestion holds

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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.