Aberrant activation of hedgehog pathway in nasopharyngeal carcinoma

Clin Exp Med. 2013 Nov;13(4):315-22. doi: 10.1007/s10238-012-0198-1. Epub 2012 Jul 20.

Abstract

Nasopharyngeal carcinoma (NPC) is a very common head and neck cancer in southern china. Despite advances in surgical and chemotherapeutic approaches, its prognosis is still not promising. Hedgehog signaling pathway was reported to be involved in a number of cancers including head and neck. However, it remains unclear regarding the role of this pathway in NPC. By real-time PCR, we found Ptch1, Smo, and Gli-1 were expressed in all human nasopharyngeal epithelial tissues and cell lines. Compared with nasopharyngeal normal epithelial tissues, the mRNA expression level of Gli-1 was higher in carcinoma and nasopharyngitis (NPI) epithelial tissues. While compared with nasopharyngitis epithelia, the mRNA expression level of Ptch1 was lower in carcinoma epithelia and normal epithelia. The expressions of Smo mRNA were not significantly different among these epithelial tissues. Immunohistochemistry analysis revealed that the expression level of Gli-1 was higher in NPC than NPI. Thus, our data indicated that aberrant activation of hedgehog pathway in NPC. Furthermore, blocking the pathway with cyclopamine inhibited the proliferation of NPC epithelia cell lines. In addition, blockade of the pathway in three NPC cell lines with cyclopamine-induced tumor cell apoptosis. The transcription of hedgehog target genes also is inhibited by cyclopamine. These data suggested that hedgehog pathway may sustain nasopharyngeal tumor growth. Our data demonstrated that hedgehog signaling pathway was involved in NPC pathogenesis and might be a novel therapeutic target for NPC.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / metabolism
  • Apoptosis
  • Biomarkers / analysis*
  • Carcinoma
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • China
  • Female
  • Gene Expression Profiling
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Nasopharyngeal Carcinoma
  • Nasopharyngeal Neoplasms / physiopathology*
  • Patched Receptors
  • Patched-1 Receptor
  • Receptors, Cell Surface / analysis*
  • Receptors, G-Protein-Coupled / analysis*
  • Signal Transduction*
  • Smoothened Receptor
  • Transcription Factors / analysis*
  • Veratrum Alkaloids / metabolism
  • Young Adult
  • Zinc Finger Protein GLI1

Substances

  • Antineoplastic Agents
  • Biomarkers
  • GLI1 protein, human
  • PTCH1 protein, human
  • Patched Receptors
  • Patched-1 Receptor
  • Receptors, Cell Surface
  • Receptors, G-Protein-Coupled
  • SMO protein, human
  • Smoothened Receptor
  • Transcription Factors
  • Veratrum Alkaloids
  • Zinc Finger Protein GLI1
  • cyclopamine