Epithelial to mesenchymal transition is activated in metastatic pheochromocytomas and paragangliomas caused by SDHB gene mutations

J Clin Endocrinol Metab. 2012 Jun;97(6):E954-62. doi: 10.1210/jc.2011-3437. Epub 2012 Apr 4.

Abstract

Context: Pheochromocytoma and paraganglioma are rare neural-crest-derived tumors. They are metastatic in 15% of cases, and the identification of a germline mutation in the SDHB gene is a predictive risk factor for malignancy and poor prognosis. To date, the link between SDHB mutations and malignancy is still missing.

Objective: Epithelial to mesenchymal transition (EMT) is a developmental event, reactivated in cancer cells to promote cell mobility and invasiveness. The aim of this study was to address the participation of EMT in the metastatic evolution of pheochromocytoma/paraganglioma.

Design and patients: Transcriptomic profiling of EMT was performed on 188 tumor samples, using a set of 94 genes implicated in this pathway. Activation of EMT was further confirmed at protein level by immunohistochemistry in a second set of 93 tumors.

Results: Hierarchical unsupervised classification showed that most SDHB-metastatic samples clustered together, indicating that EMT is differently regulated in these tumors. Major actors of EMT, metalloproteases and components of cellular junctions, were either up-regulated (LOXL2, TWIST, TCF3, MMP2, and MMP1) or down-regulated (KRT19 and CDH2) in SDHB-metastatic tumors compared with nonmetastatic ones. Interestingly, within metastatic tumors, most of these genes (LOXL2, TWIST, TCF3, MMP2, and KRT19) also allowed us to discriminate SDHB-mutated from non-SDHB-related tumors. In the second set of tumors, we studied Snail1/2 expression by immunohistochemistry and observed its specific nuclear translocation in all SDHB-metastatic tumors.

Conclusion: We have identified the first pathway that distinguishes SDHB-metastatic from all other types of pheochromocytomas/paragangliomas and suggest that activation of the EMT process might play a critical role in the particularly invasive phenotype of this group of tumors.

MeSH terms

  • Adrenal Gland Neoplasms / epidemiology
  • Adrenal Gland Neoplasms / genetics*
  • Adrenal Gland Neoplasms / pathology
  • Amino Acid Oxidoreductases / genetics
  • Amino Acid Oxidoreductases / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cell Communication / physiology
  • Epithelial-Mesenchymal Transition / genetics*
  • Gene Expression Regulation, Neoplastic
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Hypoxia / epidemiology
  • Hypoxia / genetics
  • Hypoxia / pathology
  • Intercellular Junctions / physiology
  • Mutation / genetics
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Paraganglioma / epidemiology
  • Paraganglioma / genetics*
  • Paraganglioma / pathology
  • Pheochromocytoma / epidemiology
  • Pheochromocytoma / genetics*
  • Pheochromocytoma / secondary
  • Prognosis
  • Risk Factors
  • Signal Transduction / physiology
  • Snail Family Transcription Factors
  • Succinate Dehydrogenase / genetics*
  • Succinate Dehydrogenase / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcriptome
  • Twist-Related Protein 1 / genetics
  • Twist-Related Protein 1 / metabolism

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Nuclear Proteins
  • SNAI1 protein, human
  • Snail Family Transcription Factors
  • TCF3 protein, human
  • TWIST1 protein, human
  • Transcription Factors
  • Twist-Related Protein 1
  • SDHB protein, human
  • Succinate Dehydrogenase
  • Amino Acid Oxidoreductases
  • LOXL2 protein, human