Unknown

Dataset Information

0

A chemical and genetic approach to the mode of action of fumagillin.


ABSTRACT: Previous mode of action studies identified methionine aminopeptidase 2 (MetAP-2) as the target of the antiangiogenic natural product fumagillin and its drug candidate analog, TNP-470. We report here that TNP-470-mediated MetAP-2 inhibition blocks noncanonical Wnt signaling, which plays a critical role in development, cell differentiation, and tumorigenesis. Consistent with this finding, antisense MetAP-2 morpholino oligonucleotide injection in zebrafish embryos phenocopies gastrulation defects seen in noncanonical Wnt5 loss-of-function zebrafish mutants. MetAP-2 inhibition or depletion blocks signaling downstream of the Wnt receptor Frizzled, but upstream of Calmodulin-dependent Kinase II, RhoA, and c-Jun N-terminal Kinase. Moreover, we demonstrate that TNP-470 does not block the canonical Wnt/beta-catenin pathway. Thus, TNP-470 selectively regulates noncanonical over canonical Wnt signaling and provides a unique means to explore and dissect the biological systems mediated by these pathways.

SUBMITTER: Zhang Y 

PROVIDER: S-EPMC2583369 | biostudies-literature | 2006 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications


Previous mode of action studies identified methionine aminopeptidase 2 (MetAP-2) as the target of the antiangiogenic natural product fumagillin and its drug candidate analog, TNP-470. We report here that TNP-470-mediated MetAP-2 inhibition blocks noncanonical Wnt signaling, which plays a critical role in development, cell differentiation, and tumorigenesis. Consistent with this finding, antisense MetAP-2 morpholino oligonucleotide injection in zebrafish embryos phenocopies gastrulation defects s  ...[more]

Similar Datasets

| S-EPMC6218015 | biostudies-literature
2024-02-01 | GSE239675 | GEO
| S-EPMC11375592 | biostudies-literature
2013-05-13 | E-ERAD-135 | biostudies-arrayexpress
| S-EPMC7650694 | biostudies-literature
| S-EPMC7928281 | biostudies-literature
| S-EPMC5647740 | biostudies-literature
| S-EPMC5478271 | biostudies-literature
2015-12-09 | GSE75784 | GEO
| S-EPMC6031042 | biostudies-literature