Characterization of selective and potent PI3Kδ inhibitor (PI3KD-IN-015) for B-Cell malignances

نویسندگان

  • Xiaochuan Liu
  • Aoli Wang
  • Xiaofei Liang
  • Cheng Chen
  • Juanjuan Liu
  • Zheng Zhao
  • Hong Wu
  • Yuanxin Deng
  • Li Wang
  • Beilei Wang
  • Jiaxin Wu
  • Feiyang Liu
  • Stacey M. Fernandes
  • Sophia Adamia
  • Richard M. Stone
  • Ilene A. Galinsky
  • Jennifer R. Brown
  • James D. Griffin
  • Shanchun Zhang
  • Teckpeng Loh
  • Xin Zhang
  • Wenchao Wang
  • Ellen L. Weisberg
  • Jing Liu
  • Qingsong Liu
چکیده

PI3Kδ is predominately expressed in leukocytes and has been found overexpressed in B-cell related malignances such as CLL and AML. We have discovered a highly selective ATP competitive PI3Kd inhibitor PI3KD-IN-015, which exhibits a high selectivity among other PI3K isoforms in both biochemical assays and cellular assay, meanwhile did not inhibit most of other protein kinases in the kinome. PI3KD-IN-015 demonstrates moderately anti-proliferation efficacies against a variety of B-cell related cancer cell lines through down-regulate the PI3K signaling significantly. It induced both apoptosis and autophagy in B-cell malignant cell lines. In addition, combination of autophagy inhibitor Bafilomycin could potentiate the moderate anti-proliferation effect of PI3KD-IN-015. PI3KD-IN-015 shows anti-proliferation efficacy against CLL and AML patient primary cells. Collectively, these results indicate that PI3KD-IN-015 may be useful drug candidate for further development of anti-B-cell related malignances therapies.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2016