Gene expression profiling to identify genes associated with high-invasiveness in human squamous cell carcinoma with

Koichiro Higashikawa1, Shingo Yoneda, Masayuki Taki

  • 1Department of Oral and Maxillofacial Surgery, Division of Cervico-Gnathostomatology, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3, Kasimi, Minami-ku, Hiroshima 734-8553, Japan. khigashi@hiroshima-u.ac.jp

Cancer Letters
|March 11, 2008
PubMed

Insights

The study identified 61 genes linked to tumor invasion during epithelial-to-mesenchymal transition (EMT). Snail, a key regulator, influences these genes, impacting squamous cell carcinoma (SCC) progression and invasiveness.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • Epithelial-to-mesenchymal transition (EMT) is crucial for tumor invasiveness.
  • Snail is a transcription factor that induces EMT by repressing target genes.

Purpose of the Study:

  • To define gene expression signatures associated with EMT in squamous cell carcinoma (SCC).
  • To identify invasion-associated genes regulated by Snail in SCC.

Main Methods:

  • cDNA microarray analysis was performed on human SCC cell lines with spontaneous and Snail-induced EMT.
  • Differential gene expression analysis identified 61 shared genes between EMT phenotypes.

Main Results:

  • 61 differentially expressed genes (>2- or <0.5-fold) were identified and shared across EMT cell lines.
  • These genes are implicated in development, differentiation, metabolism, apoptosis, angiogenesis, and cell adhesion.
  • Snail was confirmed to regulate pathways critical for EMT and SCC invasiveness.

Conclusions:

  • Snail plays a significant role in regulating molecular pathways that establish EMT and enhance SCC cell invasiveness.
  • The identified gene signatures provide insight into SCC progression and potential therapeutic targets.