# The Role of Mucins in Esophageal Inflammatory Diseases

**Authors:** Laura Arias-González, Alfredo J. Lucendo

PMC · DOI: 10.3390/jpm16020093 · Journal of Personalized Medicine · 2026-02-05

## TL;DR

This paper reviews how mucins in the esophagus contribute to inflammation and disease, highlighting their role in protecting and maintaining the mucosal lining.

## Contribution

The paper provides an integrated overview of mucin-driven inflammatory mechanisms in esophageal diseases.

## Key findings

- Mucins protect epithelial surfaces and maintain mucosal homeostasis by preventing pathogen adhesion.
- Aberrant mucin expression or glycosylation is linked to inflammatory disorders and cancers.
- Esophageal mucins play a key role in conditions like Barrett’s esophagus and eosinophilic esophagitis.

## Abstract

Mucins are high-molecular-weight glycoproteins that form the main structural component of the mucus covering epithelial surfaces in the gastrointestinal, respiratory, and urogenital tracts. They support epithelial integrity by protecting against microbial invasion, dehydration, and mechanical or chemical insults, while facilitating the transit of luminal contents. Beyond their structural function, mucins play key roles in molecular recognition. Their extensive glycosylation enables interactions with a wide range of molecules and allows the discrimination between pathogenic and commensal microorganisms at mucosal surfaces. Mucins help maintain mucosal homeostasis by preventing pathogen adhesion and colonization, while simultaneously providing nutrients to commensal species, supporting their stability, and maintaining spatial segregation from epithelial surfaces. Aberrant expression of mucin subtypes or alterations in their glycosylation patterns are associated with numerous diseases, including a wide spectrum of cancers and inflammatory disorders. The immunological relevance of the esophageal mucosa has only recently been recognized. Advances in the study of the esophageal mucosa-associated immune surveillance system and its interactions with structural components of this organ’s surface, including mucins, have shed light on unique pathological processes in the esophagus, such as Barrett’s esophagus, gastroesophageal reflux disease, and eosinophilic esophagitis. This review focuses on the role of esophageal mucins in inflammation, compiling current evidence to provide an integrated overview of mucin-driven inflammatory mechanisms.

## Linked entities

- **Diseases:** Barrett’s esophagus (MONDO:0013662), gastroesophageal reflux disease (MONDO:0007186), eosinophilic esophagitis (MONDO:0005361)

## Full-text entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, MUC12 (mucin 12, cell surface associated) [NCBI Gene 10071] {aka MUC-11, MUC-12, MUC11}, MUC3A (mucin 3A, cell surface associated) [NCBI Gene 4584] {aka MUC-3A, MUC3}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, MUC17 (mucin 17, cell surface associated) [NCBI Gene 140453] {aka MUC-17, MUC-3, MUC3}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, MUC1 (mucin 1, cell surface associated) [NCBI Gene 4582] {aka ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3}, ALS3 (amyotrophic lateral sclerosis 3 (autosomal dominant)) [NCBI Gene 253] {aka ALS6}, MUC6 (mucin 6, oligomeric mucus/gel-forming (gene/pseudogene)) [NCBI Gene 4588] {aka MUC-6}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, MUC5AC (mucin 5AC, oligomeric mucus/gel-forming) [NCBI Gene 4586] {aka MUC5, TBM, leB, mucin}, IL7 (interleukin 7) [NCBI Gene 3574] {aka IL-7, IMD130}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, GZMA (granzyme A) [NCBI Gene 3001] {aka CTLA3, HFSP}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, ISYNA1 (inositol-3-phosphate synthase 1) [NCBI Gene 51477] {aka INO1, INOS, IPS, IPS 1, IPS-1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, MUC20 (mucin 20, cell surface associated) [NCBI Gene 200958] {aka MUC-20}, MUC13 (mucin 13, cell surface associated) [NCBI Gene 56667] {aka DRCC1, MUC-13}, KLRK1 (killer cell lectin like receptor K1) [NCBI Gene 22914] {aka CD314, D12S2489E, KLR, NKG2-D, NKG2D}, SIGLEC8 (sialic acid binding Ig like lectin 8) [NCBI Gene 27181] {aka SAF2, SIGLEC-8, SIGLEC8L}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}, PER1 (period circadian regulator 1) [NCBI Gene 5187] {aka PER, RIGUI, hPER}, MUC21 (mucin 21, cell surface associated) [NCBI Gene 394263] {aka C6orf205, KMQK697, MUC-21}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, SIGLEC9 (sialic acid binding Ig like lectin 9) [NCBI Gene 27180] {aka CD329, CDw329, FOAP-9, OBBP-LIKE, siglec-9}, MUCIN [NCBI Gene 100508689], STAT1 (signal transducer and activator of transcription 1) [NCBI Gene 6772] {aka CANDF7, IMD31A, IMD31B, IMD31C, ISGF-3, STAT91}, MUC19 (mucin 19, oligomeric (gene/pseudogene)) [NCBI Gene 283463] {aka MUC-19}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, MICB (MHC class I polypeptide-related sequence B) [NCBI Gene 4277] {aka PERB11.2}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, MUC4 (mucin 4, cell surface associated) [NCBI Gene 4585] {aka ASGP, HSA276359, MUC-4}, MUC22 (mucin 22) [NCBI Gene 100507679] {aka PBMUCL1}, MUC3B (mucin 3B, cell surface associated) [NCBI Gene 57876] {aka MUC-3B}, MUC15 (mucin 15, cell surface associated) [NCBI Gene 143662] {aka MUC-15, PAS3, PASIII}, STAT6 (signal transducer and activator of transcription 6) [NCBI Gene 6778] {aka D12S1644, HIES6, IL-4-STAT, STAT6B, STAT6C}, MUC7 (mucin 7, secreted) [NCBI Gene 4589] {aka MG2}, MUC3 [NCBI Gene 100133790], IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, MUC2 (mucin 2, oligomeric mucus/gel-forming) [NCBI Gene 4583] {aka MLP, MUC-2, SMUC}, JAK3 (Janus kinase 3) [NCBI Gene 3718] {aka JAK-3, JAK3_HUMAN, JAKL, L-JAK, LJAK}, MUC5B (mucin 5B, oligomeric mucus/gel-forming) [NCBI Gene 727897] {aka MG1, MUC-5B, MUC5, MUC9}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** Esophageal Carcinoma (MESH:D004938), gastrointestinal, urinary tract, and joint inflammation (MESH:D014570), fungal (MESH:D009181), chronic gastritis (MESH:D005756), HIV infection (MESH:D015658), Infectious Esophagitis (MESH:D003141), chronic (MESH:D002908), aphthous stomatitis (MESH:D013281), IBD (MESH:D015212), mucosal injury (MESH:D052016), Xerostomia (MESH:D014987), bacterial infection (MESH:D001424), oral, (MESH:D020820), reflux hypersensitivity (MESH:D004342), HGD (MESH:D008228), heartburn (MESH:D006356), COVID-19 (MESH:D000086382), Esophageal Disease (MESH:D004935), infection (MESH:D007239), Crohn's disease (MESH:D003424), food allergies (MESH:D005512), NERD (MESH:D014077), polymyositis (MESH:D017285), dysphagia (MESH:D003680), rheumatoid arthritis (MESH:D001172), tumorigenic (MESH:D002471), peptic esophagitis (MESH:D004942), pyelonephritis (MESH:D011704), metabolic disease (MESH:D008659), dermatomyositis (MESH:D003882), Autoimmune Esophagitis (MESH:D004941), systemic sclerosis (MESH:D012595), systemic lupus erythematosus (MESH:D008180), HNSCC (MESH:D000077195), celiac disease (MESH:D002446), squamous cell carcinoma (MESH:D002294), regurgitation (MESH:D008944), chronic graft-versus-host disease (MESH:D000092122), autoimmune diseases (MESH:D001327), carcinogenesis (MESH:D063646), COPD (MESH:D029424), Cancer (MESH:D009369), Sjogren's syndrome (MESH:D012859), adenocarcinoma (MESH:D000230), lung cancer (MESH:D008175), intraepithelial neoplasia (MESH:D002578), asthma (MESH:D001249), head and neck or thoracic malignancies (MESH:D006258), Barrett's (MESH:D001471), fibrosis (MESH:D005355), EBV) infections (MESH:D020031), EoE (MESH:D057765), Esophageal Inflammation (MESH:D007249), enterovirus infections (MESH:D004769), GERD (MESH:D005764), injury to (MESH:D014947), dysplasia (MESH:D015792), retrosternal pain (MESH:D010146), Helicobacter pylori infection (MESH:D016481)
- **Chemicals:** alcohol (MESH:D000438), LPS (MESH:D008070), Conjugated bile acids (-), caffeine (MESH:D002110), hydrochloric acid (MESH:D006851), luminal (MESH:D010634), PGE2 (MESH:D015232), glycan (MESH:D011134), sialic acid (MESH:D019158), sugars (MESH:D000073893)
- **Species:** Aspergillus (genus) [taxon 5052], Blastomyces (genus) [taxon 229219], Cytomegalovirus (genus) [taxon 10358], Cryptococcus (genus) [taxon 79213], Mycobacterium tuberculosis (species) [taxon 1773], Helicobacter pylori (species) [taxon 210], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Homo sapiens (human, species) [taxon 9606], Streptococcus viridans (species) [taxon 78535], Solanum lycopersicum (tomato, species) [taxon 4081], Human alphaherpesvirus 3 (Varicella-zoster virus, no rank) [taxon 10335], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Human papillomavirus (species) [taxon 10566], Candida albicans (species) [taxon 5476]

## Full text

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## Figures

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## References

87 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942614/full.md

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Source: https://tomesphere.com/paper/PMC12942614