Mucin 1 downregulation associates with corticosteroid resistance in chronic rhinosinusitis with nasal polyps

J Allergy Clin Immunol. 2015 Feb;135(2):470-6. doi: 10.1016/j.jaci.2014.07.011. Epub 2014 Aug 23.

Abstract

Background: A number of patients with chronic rhinosinusitis with nasal polyps (CRSwNP) are resistant to oral corticosteroids. Mucin 1 (MUC1) shows anti-inflammatory properties, and its cytoplasmic tail (CT) interacts with transcription factors, facilitating their nuclear translocation. Because glucocorticoid receptor (GR) nuclear translocation is key to the anti-inflammatory effect of corticosteroids, we hypothesized that MUC1 is involved in the effectiveness of corticosteroids.

Objective: To analyze the role of MUC1 in corticosteroid effectiveness in different cohorts of patients with CRSwNP and elucidate the possible mechanisms involved.

Methods: Seventy-three patients with CRSwNP took oral corticosteroids for 15 days. Corticosteroid resistance was evaluated by nasal endoscopy. The expression of MUC1 and MUC1 CT was evaluated by real-time PCR, Western blotting, and immunohistochemistry. Beas-2B knockdown with RNA interference for MUC1 (siRNA-MUC1) was used to analyze the role of MUC1 in the anti-inflammatory effects of dexamethasone.

Results: Nineteen patients had nasal polyps that were resistant to oral corticosteroids (NP-CR). MUC1 expression was downregulated in these patients. Primary epithelial cells from patients with NP-CR were insensitive to the anti-inflammatory effects of dexamethasone. In siRNA-MUC1 Beas-2B, dexamethasone showed weaker anti-inflammatory effects, a reduced inhibition of phospho-extracellular-signal-regulated kinases 1/2, a less severe mitogen-activated protein kinase phosphatase 1 increase, and a reduced GR nuclear translocation. Immunoprecipitation experiments revealed that MUC1-CT and GRα form protein complexes and translocate to the nucleus in response to dexamethasone. MUC1-CT-GRα complex was downregulated in NP-CR tissue.

Conclusion: MUC1-CT participates in the corticosteroid response that mediates GRα nuclear translocation. The low expression of MUC1 in patients with CRSwNP may participate in corticosteroid resistance.

Keywords: MUC1; chronic rhinosinusitis; corticosteroid resistance; glucocorticoid receptor; nasal polyp.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use*
  • Anti-Inflammatory Agents / therapeutic use
  • Chronic Disease
  • Down-Regulation
  • Drug Resistance / genetics*
  • Gene Expression Regulation*
  • Humans
  • Mucin-1 / genetics*
  • Nasal Mucosa / drug effects
  • Nasal Mucosa / metabolism
  • Nasal Polyps / complications
  • Receptors, Glucocorticoid / genetics
  • Receptors, Glucocorticoid / metabolism
  • Rhinitis / complications
  • Rhinitis / drug therapy*
  • Rhinitis / genetics*
  • Rhinitis / metabolism
  • Signal Transduction
  • Sinusitis / complications
  • Sinusitis / drug therapy*
  • Sinusitis / genetics*
  • Sinusitis / metabolism
  • Toll-Like Receptors / genetics

Substances

  • Adrenal Cortex Hormones
  • Anti-Inflammatory Agents
  • Mucin-1
  • Receptors, Glucocorticoid
  • Toll-Like Receptors
  • glucocorticoid receptor alpha