Immunohistochemistry of thymic epithelial tumors as a tool in translational research

Thorac Surg Clin. 2011 Feb;21(1):33-46, vi. doi: 10.1016/j.thorsurg.2010.08.014.

Abstract

Due to their heterogeneity and infrequency, thymic epithelial cell tumors (TET) represent a diagnostic as well as a therapeutic problem. In the early stage of disease TET are usually cured by performing radical resections, whereas in advanced stages of disease they are usually radically unresectable from the beginning, and often show multiple relapses and/or intra- or extrathoracic metastases. Trained pathologists are required in TET diagnostics; awareness of the complexity of the mediastinum and of the differential diagnostic possibilities is mandatory. Immunohistochemical (IHC) studies play a fundamental role in oncologic surgical pathology. Among the many uses of IHC in cancer research, studies on a possible association between biomarker expression and treatment outcomes dominate the clinical translational research applications. This article reports on and discusses the role of IHC in diagnostic and translational research of TET.

Publication types

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

MeSH terms

  • Apoptosis / physiology
  • ErbB Receptors / physiology
  • Gene Expression Regulation, Neoplastic / physiology
  • Genes, p53 / physiology
  • High-Throughput Screening Assays
  • Humans
  • Immunohistochemistry
  • Neoplasm Staging
  • Neoplasms, Glandular and Epithelial* / classification
  • Neoplasms, Glandular and Epithelial* / metabolism
  • Neoplasms, Glandular and Epithelial* / pathology
  • Neovascularization, Physiologic / physiology
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Receptors, Vascular Endothelial Growth Factor / physiology
  • Thymus Neoplasms* / classification
  • Thymus Neoplasms* / metabolism
  • Thymus Neoplasms* / pathology
  • Translational Research, Biomedical / methods
  • Tumor Suppressor Protein p53 / metabolism
  • Vascular Endothelial Growth Factor A / physiology

Substances

  • Proto-Oncogene Proteins c-bcl-2
  • Tumor Suppressor Protein p53
  • Vascular Endothelial Growth Factor A
  • ErbB Receptors
  • Receptors, Vascular Endothelial Growth Factor

Supplementary concepts

  • Thymic epithelial tumor