DTIC ADA463301: AR-NcoR Interaction as a Therapeutic Target for Pro... | |
by Defense Technical Information Center | |
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Aim 1 is to determine the precise molecular basis for | |
NCoR binding to the RU486 liganded AR. Since the previous | |
report we have used chromatin immunoprecipitation to | |
demonstrate that RU486 enahnces AR NCoR recruitment to AR | |
assembled on androgen regulated genes. We have also | |
generated the additional AR and NCoR mutants to define | |
the precise amino acids mediating the interaction. Aim 2 | |
is to determine whether NCoR recruitment can suppress | |
androgen independent expression of AR regulated genes and | |
prostate cancer growth, and identify molecular markers | |
that predict whether RU486 (or related drugs) will be | |
effective in particular prostate cancers in vivo. We have | |
now used chromatin immunoprecipitation to examine the | |
functional effects of RU486 mediated NCoR recruitment, | |
and find that NCoR is not mediating deacetylation and | |
hence not suppressing gene expression. The reason for | |
this is now under investigation. These results, in | |
conjunction with our previous data, reflect further | |
progress towards determining the structural basis for AR- | |
NCoR interaction (Aim 1) and determining whether this | |
interaction can be exploited to treat prostate cancer | |
(Aim 2). | |
Date Published: 2018-06-09 20:33:48 | |
Identifier: DTIC_ADA463301 | |
Item Size: 11009255 | |
Language: english | |
Media Type: texts | |
# Topics | |
DTIC Archive; Balk, Steven P ; BETH I... | |
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@chris85 | |
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