INCB040093 Is a Novel PI3Kδ Inhibitor for the Treatment of B Cell Lymphoid Malignancies

被引:20
|
作者
Shin, Niu [1 ]
Li, Yun-Long [1 ]
Mei, Song [1 ]
Wang, Kathy He [1 ]
Hall, Leslie [1 ]
Katiyar, Kamna [1 ]
Wang, Qian [1 ]
Yang, Gengjie [1 ]
Rumberger, Beth [1 ]
Leffet, Lynn [1 ]
He, Xin [1 ]
Rupar, Mark [1 ]
Bowman, Kevin [1 ]
Favata, Margaret [1 ]
Li, Jun [1 ]
Liu, Mike [1 ]
Li, Yanlong [1 ]
Covington, Maryanne [1 ]
Koblish, Holly [1 ]
Soloviev, Maxim [1 ]
Shuey, Dana [1 ]
Burn, Timothy [1 ]
Diamond, Sharon [1 ]
Fridman, Jordan [1 ]
Combs, Andrew [1 ]
Yao, Wenqing [1 ]
Yeleswaram, Swamy [1 ]
Hollis, Gregory [1 ]
Vaddi, Kris [1 ]
Huber, Reid [1 ]
Newton, Robert [1 ]
Scherle, Peggy [1 ]
机构
[1] Incyte, Route 141 & Henry Clay Rd, Wilmington, DE 19880 USA
来源
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS | 2018年 / 364卷 / 01期
关键词
PHOSPHOINOSITIDE; 3-KINASE; PHOSPHATIDYLINOSITOL; P110-DELTA ISOFORM; ACTIVATION; CAL-101; PI3K; DIFFERENTIATION; IDELALISIB; PATHWAY; ANTIGEN;
D O I
10.1124/jpet.117.244947
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Phosphatidylinositol 3-kinase delta (PI3K delta) is a critical signaling molecule in B cells and is considered a target for development of therapies against various B cell malignancies. INCB040093 is a novel PI3Kd small-molecule inhibitor and has demonstrated promising efficacy in patients with Hodgkin's lymphoma in clinical studies. In this study, we disclose the chemical structure and the preclinical activity of the compound. In biochemical assays, INCB040093 potently inhibits the PI3K delta kinase, with 74- to >900-fold selectivity against other PI3K family members. In vitro and ex vivo studies using primary B cells, cell lines from B cell malignancies, and human whole blood show that INCB040093 inhibits PI3K delta-mediated functions, including cell signaling and proliferation. INCB040093 has no significant effect on the growth of nonlymphoid cell lines and was less potent in assays that measure human T and natural killer cell proliferation and neutrophil andmonocyte functions, suggesting that the impact of INCB040093 on the human immune system will likely be restricted to B cells. INCB040093 inhibits the production of macrophage-inflammatory protein-1 beta (MIP-1beta) and tumor necrosis factor-beta (TNF-beta) from a B cell line, suggesting a potential effect on the tumor microenvironment. In vivo, INCB040093 demonstrates single-agent activity in inhibiting tumor growth and potentiates the antitumor growth effect of the clinically relevant chemotherapeutic agent, bendamustine, in the Pfeiffer cell xenograft model of non-Hodgkin's lymphoma. INCB040093 has a favorable exposure profile in rats and an acceptable safety margin in rats and dogs. Taken together, data presented in this report support the potential utility of orally administered INCB040093 in the treatment of B cell malignancies.
引用
收藏
页码:120 / 130
页数:11
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