Journal
PLOS ONE
Volume 7, Issue 6, Pages -Publisher
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0038996
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Funding
- National Institutes of Health [R01 CA140654-01A1]
- Natural Science Foundation of Guangdong Province, P.R.C. [9451008901003072]
- Kazan, McClain, Abrams, Fernandez, Lyons, Greenwood, Harley & Oberman Foundation, Inc
- Estate of Robert Griffiths
- Jeffrey and Karen Peterson Family Foundation
- Paul and Michelle Zygielbaum
- Estate of Norman Mancini
- Barbara Isackson Lung Cancer Research Fund
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Protein kinase CK2 is frequently elevated in a variety of human cancers. The Hedgehog (Hh) signaling pathway has been implicated in stem cell maintenance, and its aberrant activation has been indicated in several types of cancer, including lung cancer. In this study, we show that CK2 is positively involved in Hh/Gli signaling in lung cancer cell lines A549 and H1299. First, we found a correlation between CK2 alpha and Gli1 mRNA levels in 100 primary lung cancer tissues. Down-regulation of Gli1 expression and transcriptional activity were demonstrated after the silencing of CK2 alpha in lung cancer cells. In addition, CK2 alpha siRNA down-regulated the expression of Hh target genes. Furthermore, two small-molecule CK2 alpha inhibitors led to a dose-dependent inhibition of Gli1 expression and transcriptional activity in lung cancer cells. Reversely, forced overexpression of CK2 alpha resulted in an increase both in Gli1 expression and transcriptional activity in A549 cells. Finally, the inhibition of Hh/Gli by CK2 alpha siRNA led to a reduction of a cancer stem cell-like side population that shows higher ABCG2 expression level. Thus, we report that the inhibition of CK2 alpha down-regulates Hh/Gli signaling and subsequently reduces stem-like side population in human lung cancer cells.
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