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HSP9O regulates cell survival via inositol hexakisphosphate kinase-2
by
Patterson, Randen L
, Sixt, Katherine M
, Koldobskiy, Michael A
, Mustafa, Asif K
, Rossum, Damian B van
, Chakraborty, Anutosh
, Juluri, Krishna R
, Snyder, Solomon H
, Snowman, Adele M
in
Apoptosis
/ Biochemistry
/ Cells
/ Chemotherapy
/ Kinases
/ Mutation
/ Proteins
2008
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HSP9O regulates cell survival via inositol hexakisphosphate kinase-2
by
Patterson, Randen L
, Sixt, Katherine M
, Koldobskiy, Michael A
, Mustafa, Asif K
, Rossum, Damian B van
, Chakraborty, Anutosh
, Juluri, Krishna R
, Snyder, Solomon H
, Snowman, Adele M
in
Apoptosis
/ Biochemistry
/ Cells
/ Chemotherapy
/ Kinases
/ Mutation
/ Proteins
2008
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Do you wish to request the book?
HSP9O regulates cell survival via inositol hexakisphosphate kinase-2
by
Patterson, Randen L
, Sixt, Katherine M
, Koldobskiy, Michael A
, Mustafa, Asif K
, Rossum, Damian B van
, Chakraborty, Anutosh
, Juluri, Krishna R
, Snyder, Solomon H
, Snowman, Adele M
in
Apoptosis
/ Biochemistry
/ Cells
/ Chemotherapy
/ Kinases
/ Mutation
/ Proteins
2008
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HSP9O regulates cell survival via inositol hexakisphosphate kinase-2
Journal Article
HSP9O regulates cell survival via inositol hexakisphosphate kinase-2
2008
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Overview
Heat-shock proteins (HSPs) are abundant, inducible proteins best known for their ability to maintain the conformation of proteins and to refold damaged proteins. Some HSPs, especially HSP90, can be antiapoptotic and the targets of anticancer drugs. Inositol hexakisphosphate kinase-2 (IP6K2), one of a family of enzymes generating the inositol pyrophosphate IP7 [diphosphoinositol pentakisphosphate (5-PP-IP5)], mediates apoptosis. Increased IP6K2 activity sensitizes cancer cells to stressors, whereas its depletion blocks cell death. We now show that HSP90 physiologically binds IP6K2 and inhibits its catalytic activity. Drugs and selective mutations that abolish HSP90-IP6K2 binding elicit activation of IP6K2, leading to cell death. Thus, the prosurvival actions of HSP90 reflect the inhibition of IP6K2, suggesting that selectively blocking this interaction could provide effective and safer modes of chemotherapy. [PUBLICATION ABSTRACT]
Publisher
National Academy of Sciences
Subject
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