Boron-Based Inhibitors of Acyl Protein Thioesterases 1 and 2

Ras proteins are of importance in cell proliferation, and hence their mutated forms play causative roles in many kinds of cancer in different tissues. Inhibition of the Ras‐depalmitoylating enzyme acyl protein thioesterases APT1 and ‐2 is a new approach to modulating the Ras cycle. Here we present b...

Full description

Saved in:
Bibliographic Details
Published inChembiochem : a European journal of chemical biology Vol. 14; no. 1; pp. 115 - 122
Main Authors Zimmermann, Tobias J., Bürger, Marco, Tashiro, Etsu, Kondoh, Yasumitsu, Martinez, Nancy E., Görmer, Kristina, Rosin-Steiner, Sigrid, Shimizu, Takeshi, Ozaki, Shoichiro, Mikoshiba, Katsuhiko, Watanabe, Nobumoto, Hall, Dennis, Vetter, Ingrid R., Osada, Hiroyuki, Hedberg, Christian, Waldmann, Herbert
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 02.01.2013
WILEY‐VCH Verlag
Wiley
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text
ISSN1439-4227
1439-7633
1439-7633
DOI10.1002/cbic.201200571

Cover

More Information
Summary:Ras proteins are of importance in cell proliferation, and hence their mutated forms play causative roles in many kinds of cancer in different tissues. Inhibition of the Ras‐depalmitoylating enzyme acyl protein thioesterases APT1 and ‐2 is a new approach to modulating the Ras cycle. Here we present boronic and borinic acid derivatives as a new class of potent and nontoxic APT inhibitors. These compounds were detected by extensive library screening using chemical arrays and turned out to inhibit human APT1 and ‐2 in a competitive mode. Furthermore, one of the molecules was demonstrated to inhibit Erk1/2 phosphorylation significantly. Ras depalmitoylation inhibitors: Different boronic and boronic acid inhibitors were found to target acyl protein thioesterases on a microarray screening chip. Individual inhibitors also display appreciable isoenzymatic specificity for APT2; this makes these boronic acids a class of APT inhibitors with specificity for one of the APTs.
Bibliography:istex:C68A9D505DC9899ADF62CE261982BB8CFE0738C7
ArticleID:CBIC201200571
Deutsche Forschungsgemeinschaft
ark:/67375/WNG-K2MCMQ5R-X
Fonds der Chemischen Industrie
These authors contributed equally to this work.
KAKEN
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:1439-4227
1439-7633
1439-7633
DOI:10.1002/cbic.201200571