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Nanoencapsulated anti-CK2 small molecule drug or siRNA specifically targets malignant cancer but not benign cells.

Janeen H Trembley | Gretchen M Unger | Vicci L Korman | Diane K Tobolt | Zygmunt Kazimierczuk | Lorenzo A Pinna | Betsy T Kren | Khalil Ahmed
Cancer letters | 2012

CK2, a pleiotropic Ser/Thr kinase, is an important target for cancer therapy. We tested our novel tenfibgen-based nanocapsule for delivery of the inhibitor 2-dimethylamino-4,5,6,7-tetrabromo-1H-benzimidazole (DMAT) and an siRNA directed against both CK2α and α' catalytic subunits to prostate cancer cells. We present data on the TBG nanocapsule itself and on CK2 inhibition or downregulation in treated cells, including effects on Nuclear Factor-kappa B (NF-κB) p65. By direct comparison of two CK2-directed cargos, our data provide proof that the TBG encapsulation design for delivery of drugs specifically to cancer cells has strong potential for small molecule- and nucleic acid-based cancer therapy.

Pubmed ID: 22050909

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Associated grants

  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK067436
  • Agency: NCI NIH HHS, United States
    Id: U01 CA015062
  • Agency: NCI NIH HHS, United States
    Id: UO1-CA15062
  • Agency: NCI NIH HHS, United States
    Id: U01 CA015062-33
  • Agency: NIDDK NIH HHS, United States
    Id: R01-DK067436
  • Agency: NCI NIH HHS, United States
    Id: R01 CA150182-01A1
  • Agency: NCI NIH HHS, United States
    Id: R01-CA150182
  • Agency: NCI NIH HHS, United States
    Id: R01 CA150182

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