Relationship between clinicopathological characteristics and CYLD expression in patients with cholesteatoma

PLoS One. 2020 Oct 8;15(10):e0240216. doi: 10.1371/journal.pone.0240216. eCollection 2020.

Abstract

Middle ear cholesteatoma is a destructive disease in which inflammation plays an important role in development and progression, and there are currently no biomarkers predicting prognosis or recurrence. Cylindromatosis (CYLD), a tumor suppressor deubiquitinase, serves as a negative regulator of inflammation expressed in tissues including the middle ear. To determine the clinical significance of CYLD in acquired cholesteatoma, we evaluated CYLD expression in acquired cholesteatoma tissue by immunostaining and analyzed its correlation with clinicopathological characteristics. Our immunohistochemical analysis revealed that CYLD expression levels were varied in the tissues of acquired cholesteatoma patients. The relative expression levels of CYLD in cholesteatoma exhibited a significant correlation with the grade of otorrhea (R = 0.532, p = 0.039). Moreover, the period of epithelialization was also significantly associated with the relative expression levels of CYLD (R = 0.720, p = 0.002). In addition, CYLD expression tended to be lower in the group with recurrence. These results suggest that low CYLD expression correlates with postoperative recovery of acquired cholesteatoma, while potentially affecting the induction of recurrence. This is the first report showing that low CYLD expression correlates with accelerated disease recovery, and suggests a new aspect of CYLD as a prognostic predictor of acquired cholesteatoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Cholesteatoma / diagnosis
  • Cholesteatoma / metabolism*
  • Cholesteatoma / pathology*
  • Deubiquitinating Enzyme CYLD / metabolism*
  • Female
  • Gene Expression Regulation, Enzymologic*
  • Humans
  • Male
  • Middle Aged
  • Prognosis

Substances

  • Deubiquitinating Enzyme CYLD

Grants and funding

This work was supported by Grants‐in‐Aid for Scientific Research (B) 18H02591 (to HJ) and by a Grant‐in‐Aid for Young Scientists (A) 26713006 (to HJ) from MEXT KAKENHI the Ministry of Education, Culture, Sports, Science and Technology of Japan.