Regulation of Fas mediated apoptosis by CD44
Date Issued
2005
Author(s)
Mielgo Iza, Ainhoa
DOI
10.5451/unibas-003683391
Abstract
Over the last decade, apoptosis has grown from an obscure process to a complex and
interesting scientific field, and many players have been identified. One of the basic
features of malignant transformation and autoimmunity is the acquisition of resistance to
apoptosis. Many reports suggest that CD44 variant isoforms exhibit an anti-apoptotic
effect leading to the progression of cancer and inflammatory diseases. However the
molecular mechanisms of CD44s and CD44v actions have so far not been elucidated.
Moreover literature about CD44 is controversial, some researchers describe CD44 as a
survival molecule, others as a pro-apoptotic protein. Probably, this controversy is due to
the presence of several isoforms and it might be possible that isoforms exhibit different
and/or even opposite functions.
The aims of this study were to elucidate the following questions:
1) Are CD44 standard and/or variant isoforms regulating Fas-mediated apoptosis
and how? (Chapter I and II).
2) Which is the in vivo implication of CD44 variant isoforms in autoimmune
diseases such as multiple sclerosis and experimental autoimmune
encephalomyelitis? (Chapter III).
To find an answer to these questions will improve our understanding of the pathogenesis
of life threatening diseases such as cancer and autoimmunity, and may open new
treatment strategies.
interesting scientific field, and many players have been identified. One of the basic
features of malignant transformation and autoimmunity is the acquisition of resistance to
apoptosis. Many reports suggest that CD44 variant isoforms exhibit an anti-apoptotic
effect leading to the progression of cancer and inflammatory diseases. However the
molecular mechanisms of CD44s and CD44v actions have so far not been elucidated.
Moreover literature about CD44 is controversial, some researchers describe CD44 as a
survival molecule, others as a pro-apoptotic protein. Probably, this controversy is due to
the presence of several isoforms and it might be possible that isoforms exhibit different
and/or even opposite functions.
The aims of this study were to elucidate the following questions:
1) Are CD44 standard and/or variant isoforms regulating Fas-mediated apoptosis
and how? (Chapter I and II).
2) Which is the in vivo implication of CD44 variant isoforms in autoimmune
diseases such as multiple sclerosis and experimental autoimmune
encephalomyelitis? (Chapter III).
To find an answer to these questions will improve our understanding of the pathogenesis
of life threatening diseases such as cancer and autoimmunity, and may open new
treatment strategies.
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