Altered expression of autophagy-related molecules and β-catenin in different subtypes of thyroid cancer: co-localization in intranuclear cytoplasmic inclusions

  • 0Department of Tumor and Diagnostic Pathology, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8523, Japan.

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Summary

This summary is machine-generated.

Autophagy molecules p62, LC3B, and β-catenin show varied expression in thyroid carcinoma (TC) subtypes. Their co-localization, especially p62 with β-catenin and LC3B, correlates with BRAF<sup>V600E</sup> mutations and may indicate autophagy dysfunction in papillary thyroid cancer.

Area Of Science

  • Oncology
  • Cell Biology
  • Molecular Pathology

Background

  • Thyroid carcinoma (TC) encompasses diverse histological types with varying prognoses.
  • Autophagy, a cellular degradation process, and its related molecules are implicated in cancer development.
  • Specific expression patterns of autophagy markers like p62, LC3B, and β-catenin in different TC subtypes remain unclear.

Purpose Of The Study

  • To investigate the expression levels and co-localization of autophagy-related molecules (β-catenin, LC3B, p62) in various thyroid carcinoma histological types.
  • To determine the association of these molecules with clinicopathological characteristics, including BRAF<sup>V600E</sup>/TERT promoter mutations and Ki-67 index.
  • To explore the potential role of these molecules in thyroid carcinogenesis and tumor aggressiveness.

Main Methods

  • Dual-color immunofluorescence analysis of β-catenin, LC3B, and p62 on 70 surgically resected thyroid nodules.
  • Inclusion of various TC types: papillary (PTC), follicular (FTC), poorly differentiated (PDTC), anaplastic (ATC), and benign controls (FA, HTT).
  • Statistical analysis to correlate marker expression and co-localization with mutations and clinicopathological features.

Main Results

  • p62 immunoreactivity was highest in papillary thyroid carcinoma (PTC), particularly classical and tall cell subtypes, co-localizing with LC3B and β-catenin within intranuclear cytoplasmic inclusions (INIs).
  • p62 expression was infrequent in follicular TC (FTC) and poorly differentiated TC (PDTC).
  • Co-localization of p62, β-catenin, and LC3B significantly correlated with BRAF<sup>V600E</sup> mutations; abnormal β-catenin expression was noted in tall cell PTC.

Conclusions

  • Distinct expression patterns of β-catenin, LC3B, and p62 exist across different thyroid carcinoma types.
  • Abnormal β-catenin expression may indicate autophagy dysfunction, potentially driving genomic instability and tumor aggressiveness.
  • These autophagy-related molecules might cooperatively contribute to INI formation during papillary thyroid carcinoma development.

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