Association between decreased WWOX protein expression and thyroid cancer development

Thyroid. 2007 Nov;17(11):1055-9. doi: 10.1089/thy.2007.0232.

Abstract

Context: Chromosomal fragile sites are often related to cancer development. The WW domain-containing oxidoreductase gene (WWOX) spans the second most common chromosomal fragile site (FRA16D) and encodes an important proapoptotic protein.

Objective: To verify our hypothesis that underexpression of WWOX could contribute to malignant transformation of the thyroid cells.

Method: We compared WWOX expression among follicular adenomas (FAs) and differentiated thyroid carcinomas [follicular thyroid carcinomas (FTCs) and papillary thyroid carcinomas (PTCs)] in 53 thyroid tumors resected from patients submitted to total thyroidectomy.

Design: Multiple fields of tumor areas of FAs, FTCs, and PTCs as well as normal thyroid tissue were stained with WWOX antiserum, and classified by the extent of staining (percentage of cells staining) and staining intensity.

Main outcome: PTCs showed a significantly decreased expression of WWOX when compared to FAs and FTCs. Further, using a unique model of comparison in patients in whom FAs and PTCs were concomitantly present, we detected the same result (i.e., no expression in PTCs).

Conclusion: We conclude that WWOX underexpression is an important step that might increase the vulnerability to the carcinogenesis process in PTCs.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma, Follicular / metabolism
  • Carcinoma, Papillary / metabolism
  • Cell Transformation, Neoplastic / metabolism
  • Chromosome Fragile Sites / physiology
  • Humans
  • Oxidoreductases / biosynthesis*
  • Thyroid Neoplasms / etiology*
  • Thyroid Neoplasms / physiopathology
  • Tumor Suppressor Proteins / biosynthesis*
  • WW Domain-Containing Oxidoreductase

Substances

  • Tumor Suppressor Proteins
  • Oxidoreductases
  • WW Domain-Containing Oxidoreductase
  • WWOX protein, human