Evidence map›Paper›PMID 42644214›Full record

ArticleJournal of food science2026

Enzymatically Hydrolyzed Eggshell Membrane Promotes Keratinocyte Differentiation Associated With PKC and Akt Signaling Pathways.

Kyohei Furukawa, Chika Ando, Tetsuro Kataoka, Yukio Hasebe, Hisanori Kato, Huijuan Jia

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Article in Journal of food science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

5 · Who and what money

Authors and funding

6 authors.

Kyohei FurukawaGraduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0226-1277
Chika AndoGraduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
Tetsuro KataokaGraduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
Yukio HasebeALMADO Inc., Tokyo, Japan.
Hisanori KatoGraduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
Huijuan JiaGraduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9920-8340

Funding

Kieikai Research Foundation
6 · The paper itself

Abstract

Skin aging is characterized by physiological and morphological changes, and nutritional interventions are key strategies to mitigate this process. Eggshell membrane (ESM), a natural byproduct of egg processing, is typically discarded as industrial waste; however, recent studies have revealed its health benefits, including antiobesity and anti-inflammatory effects. We previously reported that enzymatically hydrolyzed ESM (eESM) promotes keratinocyte differentiation in NHEK-Neo cells, although the underlying mechanisms remain unclear. In this study, we show that treatment of NHEK-Neo cells with varying concentrations of eESM upregulated keratinocyte differentiation markers (KRT1, KRT10, IVL, FLG, KRT13) and induced dose-dependent morphological changes. Calcium, a key regulator of keratinocyte differentiation, is present in eESM. Supplementation of calcium significantly increased transcription of early differentiation markers (KRT1, KRT10) but had little effect on late markers (IVL, FLG, KRT13), suggesting that additional bioactive components in eESM contribute to differentiation. Furthermore, eESM enhanced the expression of PKC-related genes (IRF6, GRHL3, OVOL1) and increased phosphorylation of Akt and ERK2. Pharmacological inhibition of PKC and Akt signaling suppressed keratinocyte differentiation. Ultra-high-performance liquid chromatography analysis further suggested that eESM may contain components with a molecular weight of approximately 1000 Da, although further characterization is required. Collectively, these findings indicate that eESM promotes keratinocyte differentiation associated with PKC and Akt signaling pathways, likely through the coordinated action of calcium and other bioactive molecules, and that the observed effects cannot be attributed to calcium alone. eESM may, therefore, represent a potential food-derived functional ingredient for skin health.

Indexed as

Cell DifferentiationEgg ShellKeratinocytesProtein Kinase CProto-Oncogene Proteins c-aktAnimalsCalciumCell LineFilaggrin ProteinsHumansHydrolysisPhosphorylationSignal TransductionCalciumFilaggrin ProteinsFLG protein, humanProtein Kinase CProto-Oncogene Proteins c-akt

Identifiers

PMID42644214
PMCPMC13507864

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.