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

被引:5
|
作者
Liu, Xiaochuan [1 ,2 ]
Wang, Aoli [2 ,3 ]
Liang, Xiaofei [2 ,4 ]
Chen, Cheng [2 ,4 ]
Liu, Juanjuan [2 ,3 ]
Zhao, Zheng [2 ,4 ]
Wu, Hong [2 ,3 ]
Deng, Yuanxin [2 ,3 ]
Wang, Li [2 ,4 ]
Wang, Beilei [2 ,4 ]
Wu, Jiaxin [2 ,3 ]
Liu, Feiyang [2 ,3 ]
Fernandes, Stacey M. [5 ]
Adamia, Sophia [5 ]
Stone, Richard M. [5 ]
Galinsky, Ilene A. [5 ]
Brown, Jennifer R. [5 ]
Griffin, James D. [5 ]
Zhang, Shanchun [4 ,6 ]
Loh, Teckpeng [1 ]
Zhang, Xin [2 ]
Wang, Wenchao [2 ,4 ]
Weisberg, Ellen L. [5 ]
Liu, Jing [2 ,4 ]
Liu, Qingsong [2 ,4 ,7 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei 230036, Anhui, Peoples R China
[2] Chinese Acad Sci, High Field Magnet Lab, Hefei 230031, Anhui, Peoples R China
[3] Univ Sci & Technol China, Hefei 230036, Anhui, Peoples R China
[4] CHMFL HCMTC Target Therapy Joint Lab, Hefei 230031, Anhui, Peoples R China
[5] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, 44 Binney St, Boston, MA 02115 USA
[6] Hefei Cosource Med Technol Co LTD, Hefei 230031, Anhui, Peoples R China
[7] Chinese Acad Sci, Hefei Sci Ctr, Hefei 230031, Anhui, Peoples R China
关键词
PI3K delta; leukemia; B-cell malignances; PI3K; kinase inhibitors; CHRONIC LYMPHOCYTIC-LEUKEMIA; PI3K; P110-DELTA; IDELALISIB; 3-KINASES; SURVIVAL; ISOFORM; CANCER;
D O I
10.18632/oncotarget.8702
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PI3K delta 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 PI3K delta 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 antiproliferation 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.
引用
收藏
页码:32641 / 32651
页数:11
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