Inhibition of CK2α down-regulates Notch1 signalling in lung cancer cells

J Cell Mol Med. 2013 Jul;17(7):854-62. doi: 10.1111/jcmm.12068. Epub 2013 May 8.

Abstract

Protein kinase CK2 is frequently elevated in a variety of human cancers. The Notch1 signalling pathway has been implicated in stem cell maintenance and its aberrant activation has been shown in several types of cancer including lung cancer. Here, we show, for the first time, that CK2α is a positive regulator of Notch1 signalling in lung cancer cell lines A549 and H1299. We found that Notch1 protein level was reduced after CK2α silencing. Down-regulation of Notch1 transcriptional activity was demonstrated after the silencing of CK2α in lung cancer cells. Furthermore, small-molecule CK2α inhibitor CX-4945 led to a dose-dependent inhibition of Notch1 transcriptional activity. Conversely, forced overexpression of CK2α resulted in an increase in Notch1 transcriptional activity. Finally, the inhibition of CK2α led to a reduced proportion of stem-like CD44 + /CD24- cell population. Thus, we report that the inhibition of CK2α down-regulates Notch1 signalling and subsequently reduces a cancer stem-like cell population in human lung cancer cells. Our data suggest that CK2α inhibitors may be beneficial to the lung cancer patients with activated Notch1 signalling.

Keywords: CD44 + /CD24−; CK2α; Notch1; cancer stem cell; lung cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD24 Antigen / metabolism
  • Casein Kinase II / antagonists & inhibitors*
  • Casein Kinase II / metabolism
  • Cell Line, Tumor
  • DNA / metabolism
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Flow Cytometry
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Hyaluronan Receptors / metabolism
  • Immunohistochemistry
  • Lung Neoplasms / metabolism*
  • Naphthyridines / pharmacology
  • Neoplastic Stem Cells / cytology
  • Phenazines
  • Phenotype
  • RNA, Small Interfering / metabolism
  • Receptor, Notch1 / metabolism*
  • Signal Transduction*
  • Transcription, Genetic

Substances

  • CD24 Antigen
  • Hyaluronan Receptors
  • NOTCH1 protein, human
  • Naphthyridines
  • Phenazines
  • RNA, Small Interfering
  • Receptor, Notch1
  • DNA
  • silmitasertib
  • Casein Kinase II