The role of human achaete-scute homolog-1 in medullary thyroid cancer cells

Surgery. 2003 Dec;134(6):866-71; discussion 871-3. doi: 10.1016/s0039-6060(03)00418-5.

Abstract

Background: Human achaete-scute homolog-1 (hASH1) is a transcription factor that is expressed highly in neuroendocrine tumors such as medullary thyroid cancer (MTC). Thyroid C-cells do not develop in hASH1 knockout mice, which suggests that hASH1 is essential for normal C-cell development.

Methods: To determine the effect of raf-1 induction on hASH1 and hormone production, we used an estrogen inducible raf-1 construct in MTC cell line (TT) cells (TT-raf cells). TT or TT-raf cells were treated with control or 1 microM estradiol. After 48 hours, the cells were analyzed for levels of hASH1 and chromogranin A by Western blotting and for calcitonin production by enzyme-linked immunosorbent assay.

Results: Activation of raf-1 in the TT-raf cells resulted in high levels of phosphorylated MEK and ERK1/2, a morphologic transdifferentiation, and a decrease in chromogranin A and calcitonin levels that are associated with a reduction in hASH1 production. Furthermore, using MEK inhibitors, we demonstrated that these raf-1-mediated changes are dependent on MEK but not ERK1/2 activation.

Conclusion: hASH1 down-regulation by raf-1 in MTC cells is associated with a significant decrease in hormone production. Thus, hASH1 appears to be important in the endocrine phenotype of MTC tumors and may serve as a molecular target for the treatment of patients with MTC.

Publication types

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

MeSH terms

  • Basic Helix-Loop-Helix Transcription Factors
  • Calcitonin / metabolism
  • Carcinoma, Medullary / metabolism*
  • Carcinoma, Medullary / pathology
  • Cell Differentiation
  • Cell Line, Tumor
  • DNA-Binding Proteins / physiology*
  • Down-Regulation
  • Humans
  • Phenotype
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins c-raf / metabolism*
  • Thyroid Neoplasms / metabolism*
  • Thyroid Neoplasms / pathology
  • Transcription Factors / physiology*

Substances

  • ASCL1 protein, human
  • Basic Helix-Loop-Helix Transcription Factors
  • DNA-Binding Proteins
  • Transcription Factors
  • Calcitonin
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-raf