CK2 pro-survival role in prostate cancer is mediated via maintenance and promotion of androgen receptor and NFκB p65 expression

Janeen H. Trembley, Betsy T. Kren, Md J. Abedin, Daniel P. Shaughnessy, Yingming Li, Scott M. Dehm, Khalil Ahmed

Research output: Contribution to journalArticlepeer-review

11 Scopus citations


The prosurvival protein kinase CK2, androgen receptor (AR), and nuclear factor kappa B (NFκB) interact in the function of prostate cells, and there is evidence of crosstalk between these signals in the pathobiology of prostate cancer (PCa). As CK2 is elevated in PCa, and AR and NFκB are involved in the development and progression of prostate cancer, we investigated their interaction in benign and malignant prostate cells in the presence of altered CK2 expression. Our results show that elevation of CK2 levels caused increased levels of AR and NFκB p65 in prostate cells of different phenotypes. Analysis of TCGA PCa data indicated that AR and CK2α RNA expression are strongly correlated. Small molecule inhibition or molecular down-regulation of CK2 caused reduction in AR mRNA expression and protein levels in PCa cells and in orthotopic xenograft tumors by various pathways. Among these, regulation of AR protein stability plays a unifying role in CK2 maintenance of AR protein levels. Our results show induction of various endoplasmic reticulum stress signals after CK2 inhibition, which may play a role in the PCa cell death response. Of note, CK2 inhibition caused loss of cell viability in both parental and enzalutamide-resistant castrate-resistant PCa cells. The present work elucidates the specific link of CK2 to the pathogenesis of PCa in association with AR and NFκB expression; further, the observation that inhibition of CK2 can exert a growth inhibitory effect on therapy-resistant PCa cells emphasizes the potential utility of CK2 inhibition in patients who are on enzalutamide treatment for advanced cancer.

Original languageEnglish (US)
Article number89
Issue number2
StatePublished - Jun 2019

Bibliographical note

Funding Information:
Funding: This work was supported by Merit Review research funds BX003282 awarded by the Department of Veterans Affairs (K.A.), and research grant R01CA150182 awarded by the National Cancer Institute, NIH, Department of Health and Human Services (K.A.).

Publisher Copyright:
© 2019 by the authors. Licensee MDPI, Basel, Switzerland.


  • AR
  • CK2
  • CRPC
  • Cell death
  • In vivo delivery
  • Mitochondria
  • Nanocapsule
  • Nanoparticle
  • Prostate
  • Survival
  • Tenfibgen
  • Xenograft


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