ErbB receptors in the biology and pathology of the aerodigestive tract

Exp Cell Res. 2009 Feb 15;315(4):572-82. doi: 10.1016/j.yexcr.2008.08.009. Epub 2008 Aug 23.

Abstract

The most common sites of malignancies in the aerodigestive tract include the lung, head and neck and the esophagus. Esophageal adenocarcinomas (EA), esophageal squamous cell carcinomas (ESCC), and squamous cell carcinomas of the head and neck (SCCHN) are the primary focus of this review. Traditional treatment for aerodigestive tract cancers includes primary chemoradiotherapy (CRT) or surgical resection followed by radiation (or CRT). Recent developments in treatment have focused increasingly on molecular targeting strategies including cetuximab (a monoclonal antibody against epidermal growth factor receptor (EGFR)). Cetuximab was FDA approved in 2006 for treatment of SCCHN, underscoring the importance of understanding the biology of these malignancies. EGFR is a member of the ErbB family of growth factor receptor tyrosine kinases. The major pathways activated by ErbB receptors include Ras/Raf/MAPK; PI3K/AKT; PLCgamma and STATs, all of which lead to the transcription of target genes that may contribute to aerodigestive tumor progression. This review explores the expression of ErbB receptors in EA, ESCC and SCCHN and the signaling pathways of EGFR in SCCHN.

Publication types

  • Review

MeSH terms

  • Drug Delivery Systems
  • ErbB Receptors / metabolism
  • Esophageal Neoplasms / drug therapy
  • Esophageal Neoplasms / physiopathology
  • Gene Expression Regulation, Neoplastic
  • Head and Neck Neoplasms / drug therapy
  • Head and Neck Neoplasms / physiopathology*
  • Humans
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / physiopathology
  • Oncogene Proteins v-erbB / classification
  • Oncogene Proteins v-erbB / metabolism*
  • STAT Transcription Factors / metabolism
  • Signal Transduction
  • src-Family Kinases / metabolism

Substances

  • Oncogene Proteins v-erbB
  • STAT Transcription Factors
  • ErbB Receptors
  • src-Family Kinases