Biomarkers of aggressive pituitary adenomas

J Mol Endocrinol. 2012 Aug 30;49(2):R69-78. doi: 10.1530/JME-12-0113. Print 2012 Oct.

Abstract

Pituitary adenomas exhibit a wide range of behaviors. The prediction of aggressive or malignant behavior in pituitary adenomas remains challenging; however, the utility of biomarkers is rapidly evolving. In this review, we discuss potential biomarkers as they relate to aggressive behavior in pituitary adenomas. While detailed histological subtyping remains the best independent predictor of aggressive behavior in the majority of cases, evidence suggests that the additional analyses of FGFR4, MMP, PTTG, Ki-67, p53, and deletions in chromosome 11 may contribute to decisions concerning management of aggressive pituitary adenomas.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenoma / genetics*
  • Adenoma / metabolism
  • Adenoma / pathology*
  • Biomarkers, Tumor / analysis*
  • Biomarkers, Tumor / genetics
  • Carrier Proteins / genetics
  • Chromosome Deletion
  • Chromosomes, Human, Pair 11
  • Genes, p53
  • Humans
  • Ki-67 Antigen / analysis
  • Matrix Metalloproteinases / analysis
  • Matrix Metalloproteinases / genetics
  • MicroRNAs
  • Mutation
  • Neoplasm Proteins / genetics
  • Pituitary Neoplasms / genetics*
  • Pituitary Neoplasms / metabolism
  • Pituitary Neoplasms / pathology*
  • Receptor, Fibroblast Growth Factor, Type 4 / analysis
  • Receptor, Fibroblast Growth Factor, Type 4 / genetics
  • Securin

Substances

  • Biomarkers, Tumor
  • Carrier Proteins
  • Ki-67 Antigen
  • MicroRNAs
  • Neoplasm Proteins
  • Securin
  • pituitary tumor-transforming protein 1, human
  • FGFR4 protein, human
  • Receptor, Fibroblast Growth Factor, Type 4
  • Matrix Metalloproteinases
  • somatotropin-binding protein