Title
Zoledronic Acid Inhibits Cancer Growth: Molecular Characterization Of Zoledronic Acid Induced Growth Inhibition In Cancer,Used
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The aminobisphosphonate zoledronic acid(ZOL) has elicited significant attention due to its remarkable antitumoral activity,though its detailed mechanism of action remains unclear. Here,we demonstrate the existence of a nuclear GSK3NFATc2 stabilization pathway that promotes cancer growth in vitro and in vivo and serves as a bonafide target of ZOL. Specifically, the serine/threonine kinase GSK3 stabilizes nuclear NFATc2 through phosphorylation of the serinerich SP2 domain, thus protecting the transcription factor from E3ubiquitin ligase HDM2 mediated proteolysis. ZOL disrupts this NFATc2 stabilization pathway through two mechanisms, namely GSK3 inhibition and induction of HDM2 activity. Upon nuclear accumulation,HDM2 targets unphosphorylated NFATc2 for ubiquitination at acceptor lysine residues K684/K897 and hence labels the factor for subsequent proteasomal degradation. Conversely, mutagenesis induced constitutive serine phosphorylation of the SP2 domain prevents NFATc2 from HDM2 mediated ubiquitination and degradation by ZOL. In conclusion, this report demonstrates a critical role of the GSK3HDM2 signaling loop in the regulation of NFATc2 protein stability.
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We provide a 2-year limited warranty, from the date of purchase for all our products.
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This warranty strictly does not cover damages that arose from negligence, misuse, wear and tear, or not in accordance with product instructions (dropping the product, etc.).
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