Molecular Pathways: Targeting Phosphoinositide 3-Kinase p110-Delta in Chronic Lymphocytic Leukemia
被引:42
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作者:
Herman, Sarah E. M.
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NHLBI, Hematol Branch, NIH, Bethesda, MD 20892 USAOhio State Univ, Coll Pharm, Div Hematol, Dept Internal Med, Columbus, OH 43210 USA
Herman, Sarah E. M.
[2
]
Johnson, Amy J.
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Ohio State Univ, Coll Pharm, Div Hematol, Dept Internal Med, Columbus, OH 43210 USA
Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USAOhio State Univ, Coll Pharm, Div Hematol, Dept Internal Med, Columbus, OH 43210 USA
Johnson, Amy J.
[1
,3
]
机构:
[1] Ohio State Univ, Coll Pharm, Div Hematol, Dept Internal Med, Columbus, OH 43210 USA
[2] NHLBI, Hematol Branch, NIH, Bethesda, MD 20892 USA
[3] Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA
The advent of targeted therapy, specifically to the B-cell receptor (BCR), has changed the convention for the treatment of chronic lymphocytic leukemia (CLL). The phosphoinositide 3-kinase (PI3K) pathway, activated upstream by the BCR, receptor tyrosine kinases, and cytokine receptors, has been a potential target for a multitude of cancers, but until the recent introduction of isoform-specific inhibitors has not been widely used. In this review, we focus on describing the intricate upstream and downstream signaling, leading to cell survival mediated by PI3K in B cells with a specific focus on the impact and importance of the p110 delta isoform (which is localized to hematopoietic cells and regulates distinct cellular functions in B cells). In addition, the clinical advances from targeting p110 delta are described, with a focus on clinical outcome, toxicities, and rational combination therapies. The experiences with p110 delta in CLL have led to a more fundamental understanding of CLL signaling defects and may be predictive of other BCR-directed therapeutics. Clin Cancer Res; 18(15); 4013-8. (C)2012 AACR.
机构:
Northwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
Northwestern Univ, Sch Med, Div Hematol Oncol, Chicago, IL 60611 USA
Virginia Med Ctr, Chicago, IL USANorthwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
Goussetis, Dennis J.
Platanias, Leonidas C.
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Northwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
Northwestern Univ, Sch Med, Div Hematol Oncol, Chicago, IL 60611 USA
Virginia Med Ctr, Chicago, IL USANorthwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
机构:
Univ Auckland, Fac Med & Hlth Sci, Auckland Canc Soc Res Ctr, Auckland 1042, New Zealand
Univ Auckland, Maurice Wilkins Ctr Mol Biodiscovery, Auckland 1042, New ZealandUniv Auckland, Fac Med & Hlth Sci, Auckland Canc Soc Res Ctr, Auckland 1042, New Zealand
Flanagan, Jack U.
Shepherd, Peter R.
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Univ Auckland, Fac Med & Hlth Sci, Auckland Canc Soc Res Ctr, Auckland 1042, New Zealand
Univ Auckland, Maurice Wilkins Ctr Mol Biodiscovery, Auckland 1042, New Zealand
Univ Auckland, Sch Med, Dept Mol Med & Pathol, Auckland 1042, New ZealandUniv Auckland, Fac Med & Hlth Sci, Auckland Canc Soc Res Ctr, Auckland 1042, New Zealand
机构:
Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol,CLL Ctr, Boston, MA 02215 USAHarvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol,CLL Ctr, Boston, MA 02215 USA
Davids, Matthew S.
Brown, Jennifer R.
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Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol,CLL Ctr, Boston, MA 02215 USAHarvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol,CLL Ctr, Boston, MA 02215 USA
机构:
Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan
Tamura, Namiko
Hazeki, Kaoru
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Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan
Hazeki, Kaoru
Okazaki, Natsumi
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Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan
Okazaki, Natsumi
Kametani, Yukiko
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Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan
Kametani, Yukiko
Murakami, Hiroki
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Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan
Murakami, Hiroki
Takaba, Yuki
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Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan
Takaba, Yuki
Ishikawa, Yuki
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Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan
Ishikawa, Yuki
Nigorikawa, Kiyomi
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Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan
Nigorikawa, Kiyomi
Hazeki, Osamu
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Hiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, JapanHiroshima Univ, Div Mol Med Sci, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348553, Japan