Correlation Engine 2.0
Clear Search sequence regions


  • adenoid (6)
  • breast cancer (1)
  • cell movement (1)
  • chromatin (1)
  • factors (6)
  • family (2)
  • gene (1)
  • glioma (1)
  • human (2)
  • plicamycin (2)
  • plicamycin (6)
  • protein human (2)
  • SNAI1 (6)
  • SP1 (4)
  • Sizes of these terms reflect their relevance to your search.

    Mithramycin exhibits certain anticancer effects in glioma, metastatic cerebral carcinoma, malignant lymphoma, chorionic carcinoma and breast cancer. However, its effects on salivary adenoid cystic carcinoma remain unclear. Here, we report that mithramycin significantly inhibited epithelial-to-mesenchymal transition and invasion in human salivary adenoid cystic carcinoma cell lines. The underlying mechanism for this activity was further demonstrated to involve decreasing the expression of the transcription factors specificity protein 1 and SNAI1. Specificity protein 1 is a pro-tumourigenic transcription factor that is overexpressed in SACC-LM and SACC-83 cells, and its expression is inhibited by mithramycin. Moreover, chromatin immunoprecipitation assays showed that specificity protein 1 induced SNAI1 transcription through direct binding to the SNAI1 promoter. In summary, this study uncovered the mechanism through which mithramycin inhibits epithelial-to-mesenchymal transition and invasion in salivary adenoid cystic carcinoma cell lines, namely, via downregulating specificity protein 1 and SNAI1 expression, which suggests mithramycin may be a promising therapeutic option for salivary adenoid cystic carcinoma.

    Citation

    Jiasu Li, Hongmei Gao, Lingxu Meng, Lin Yin. Mithramycin inhibits epithelial-to-mesenchymal transition and invasion by downregulating SP1 and SNAI1 in salivary adenoid cystic carcinoma. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 2017 Jun;39(6):1010428317708697

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 28631560

    View Full Text