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Necroptosis: Biochemical, Physiological and Pathological Aspects

Journal

PATHOLOGY & ONCOLOGY RESEARCH
Volume 17, Issue 4, Pages 791-800

Publisher

SPRINGER
DOI: 10.1007/s12253-011-9433-4

Keywords

Necrosis; Necroptosis; Programmed cell death; RIPK1; RIPK3; TNF; Death receptor

Funding

  1. [ETT 016/2008]

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Programmed cell death is a key component of tissue homeostasis, normal development and wide variety of diseases. Conventional view refers to programmed cell death form as caspase-mediated apoptosis while necrosis is considered as an accidental and unwanted cell demise, carried out in a non-regulated manner and caused by extreme conditions. However, accumulating evidences indicate that necrotic cell death can also be a regulated process. The term necroptosis has been introduced to describe a cell death receptor-induced, caspase-independent, highly regulated type of programmed cell death process with morphological resemblance of necrosis. Necroptosis recently has been found to contribute to a wide range of pathologic cell death forms including ischemic brain injury, neurodegenerative diseases and viral infection, therefore a better understanding of the necroptotic signaling machinery has clinical relevance.

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