Over the past decade, the Hippo signaling cascade has been linked to organ size regulation in mammals. Indeed, modulation of the Hippo pathway can have potent effects on cellular proliferation and/or apoptosis and a deregulation of the pathway often leads to tumor development. Importantly, emerging evidence indicates that the Hippo pathway can modulate its effects on tissue size by the regulation of stem and progenitor cell activity. This role has recently been associated with the central position of the pathway in sensing spatiotemporal or mechanical cues, and translating them into specific cellular outputs. These results provide an attractive model for how the Hippo cascade might sense and transduce cellular 'neighborhood' cues into activation of tissue-specific stem or progenitors cells. A further understanding of this process could allow the development of new therapies for various degenerative diseases and cancers. Here, we review current and emerging data linking Hippo signaling to progenitor cell function. (C) 2012 Elsevier Ltd. All rights reserved.
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Mem Sloan Kettering Canc Ctr, Mol Cytol Core Facil, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Fujisawa, Sho
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Barlas, Afsar
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Mem Sloan Kettering Canc Ctr, Mol Cytol Core Facil, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Barlas, Afsar
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Miller, Alexandria N.
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Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Miller, Alexandria N.
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Manova-Todorova, Katia
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Mem Sloan Kettering Canc Ctr, Mol Cytol Core Facil, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Manova-Todorova, Katia
;
Macias, Maria J.
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Inst Biomed Res, Struct & Computat Biol Programme, Barcelona 08028, SpainHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Macias, Maria J.
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Sapkota, Gopal
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Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Sapkota, Gopal
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Pan, Duojia
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Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Pan, Duojia
;
Massague, Joan
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Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
机构:
Mem Sloan Kettering Canc Ctr, Mol Cytol Core Facil, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Fujisawa, Sho
;
Barlas, Afsar
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h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Mol Cytol Core Facil, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Barlas, Afsar
;
Miller, Alexandria N.
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机构:
Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Miller, Alexandria N.
;
Manova-Todorova, Katia
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机构:
Mem Sloan Kettering Canc Ctr, Mol Cytol Core Facil, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Manova-Todorova, Katia
;
Macias, Maria J.
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机构:
Inst Biomed Res, Struct & Computat Biol Programme, Barcelona 08028, SpainHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Macias, Maria J.
;
Sapkota, Gopal
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h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Sapkota, Gopal
;
Pan, Duojia
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h-index: 0
机构:
Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA
Pan, Duojia
;
Massague, Joan
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h-index: 0
机构:
Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10021 USAHoward Hughes Med Inst, Chevy Chase, MD 20815 USA