Unknown

Dataset Information

0

Design, synthesis, and biological evaluation of substrate-competitive inhibitors of C-terminal Binding Protein (CtBP).


ABSTRACT: C-terminal Binding Protein (CtBP) is a transcriptional co-regulator that downregulates the expression of many tumor-suppressor genes. Utilizing a crystal structure of CtBP with its substrate 4-methylthio-2-oxobutyric acid (MTOB) and NAD(+) as a guide, we have designed, synthesized, and tested a series of small molecule inhibitors of CtBP. From our first round of compounds, we identified 2-(hydroxyimino)-3-phenylpropanoic acid as a potent CtBP inhibitor (IC50=0.24?M). A structure-activity relationship study of this compound further identified the 4-chloro- (IC50=0.18?M) and 3-chloro- (IC50=0.17?M) analogues as additional potent CtBP inhibitors. Evaluation of the hydroxyimine analogues in a short-term cell growth/viability assay showed that the 4-chloro- and 3-chloro-analogues are 2-fold and 4-fold more potent, respectively, than the MTOB control. A functional cellular assay using a CtBP-specific transcriptional readout revealed that the 4-chloro- and 3-chloro-hydroxyimine analogues were able to block CtBP transcriptional repression activity. This data suggests that substrate-competitive inhibition of CtBP dehydrogenase activity is a potential mechanism to reactivate tumor-suppressor gene expression as a therapeutic strategy for cancer.

SUBMITTER: Korwar S 

PROVIDER: S-EPMC4993153 | biostudies-literature | 2016 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Design, synthesis, and biological evaluation of substrate-competitive inhibitors of C-terminal Binding Protein (CtBP).

Korwar Sudha S   Morris Benjamin L BL   Parikh Hardik I HI   Coover Robert A RA   Doughty Tyler W TW   Love Ian M IM   Hilbert Brendan J BJ   Royer William E WE   Kellogg Glen E GE   Grossman Steven R SR   Ellis Keith C KC  

Bioorganic & medicinal chemistry 20160420 12


C-terminal Binding Protein (CtBP) is a transcriptional co-regulator that downregulates the expression of many tumor-suppressor genes. Utilizing a crystal structure of CtBP with its substrate 4-methylthio-2-oxobutyric acid (MTOB) and NAD(+) as a guide, we have designed, synthesized, and tested a series of small molecule inhibitors of CtBP. From our first round of compounds, we identified 2-(hydroxyimino)-3-phenylpropanoic acid as a potent CtBP inhibitor (IC50=0.24μM). A structure-activity relatio  ...[more]

Similar Datasets

| S-EPMC4406240 | biostudies-literature
| S-EPMC5214847 | biostudies-literature
| S-EPMC4329597 | biostudies-literature
| S-EPMC4161160 | biostudies-literature
| S-EPMC5892432 | biostudies-literature
| S-EPMC4349528 | biostudies-literature
| S-EPMC3244726 | biostudies-literature
| S-EPMC6274369 | biostudies-literature
| S-EPMC3049263 | biostudies-literature
| S-EPMC2667321 | biostudies-literature