Evidence map›Paper›PMID 41581037›Full record

ArticleIndian journal of ophthalmology2026

Differential expression of transcription factors in moderate and severe Fuchs endothelial corneal dystrophy.

Srividya Gurumurthy, Prema Padmanabhan, Narayanasamy Angayarkanni

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Article in Indian journal of ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Srividya GurumurthyR. S. Mehta Jain Department of Biochemistry and Cell Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu.
Prema PadmanabhanCJ Shah Cornea Services, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India.
Narayanasamy AngayarkanniR. S. Mehta Jain Department of Biochemistry and Cell Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeFuchs endothelial corneal dystrophy (FECD) results in the death of the nonproliferative endothelial cells of the posterior corneal surface, leading to corneal swelling, clouding, and potential blindness. Few studies have suggested the potential role of transcription factors in the endothelial to mesenchymal transition (EnMT) during disease progression. This study aimed to evaluate the expression of selected transcription factors in the corneal endothelium of FECD patients to understand their role in disease pathogenesis.

designThis is a prospective, pilot, case-control study for studying the gene expression in patients with FECD. Transcription factors ZEB1, TCF4, smad proteins (SMAD3, SMAD4), zinc finger proteins SNAI1 and SNAI2, lymphoid enhancer binding factor 1 (LEF1), N-cadherin (CDH2), claudin 10 (CLDN10), and nuclear factor (erythroid-derived 2)-like 2 (NFE2L2/NRF2), which are involved in the EnMT, were selected for the study. Fourteen FECD endothelia were compared with 15 control endothelia for the gene expression analyses using quantitative real-time PCR.

resultsSignificant differential expressions were seen in the levels of SMAD3 (P = 0.0251) in moderate cases compared to control tissues. Further, TCF4 and NFE2L2 showed significantly different expressions among the moderate and severe cases (P = 0.0262 and P = 0.0350, respectively), with expressions decreasing with severity, indicating their possible role in disease progression.

conclusionsOur pilot study on transcription factor gene expressions in FECD patients' tissue samples suggests NRF2 and TCF4 to play an important role in the disease pathogenesis and progression.

Indexed as

DNAEndothelium, CornealFuchs' Endothelial DystrophyGene Expression RegulationRNATranscription FactorsAgedCase-Control StudiesEndothelial-Mesenchymal TransitionFemaleHumansMaleMiddle AgedPilot ProjectsProspective StudiesReal-Time Polymerase Chain ReactionDNARNATranscription FactorsDifferential gene expressionepithelial to mesenchymal transitionoxidative stresstranscription factors

Identifiers

PMID41581037
PMCPMC12947105

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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.