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GENES & DEVELOPMENT 17:2481-2495, 2003
©2003 by Cold Spring Harbor Laboratory Press; ISSN 0890-9369/ $5.00
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REVIEW

Ways of dying: multiple pathways to apoptosis

Jerry M. Adams1

The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia

The first 100 words of the full text of this article appear below.

In order to eliminate cells that are redundant, damaged, or infected, metazoan organisms have evolved the cell suicide mechanism termed apoptosis (Kerr et al. 1972Go). This genetic program is vital for normal development, for maintenance of tissue homeostasis, and for an effective immune system. Not surprisingly therefore, its disturbance is implicated in numerous pathological conditions, ranging from degenerative disorders to autoimmunity and cancer (Cory and Adams 2002Go; Cory et al. 2003Go).

The cell's death throes are choreographed by a set of previously dormant proteases, the caspases, which cleave several hundred cellular substrates (Thornberry and Lazebnik 1998Go). . . . [Full Text of this Article]


    The demolition machinery
 

    The Bcl-2 family of apoptotic regulators
 

    The mitochondrial `poison cabinet'
 

    Amplification role of the apoptosome
 

    Potential role of the ER in apoptosis
 

    Potential apoptotic roles of initiator caspases other than caspase-9
 

Caspase-12


Caspase-2


Caspase-1 and caspase-11


Caspase-8


    Interplay of Bcl-2 family members in commitment to apoptosis
 

    How might the Bcl-2 family control the activation of caspases?
 

    Conclusions and conundrums
 

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