Unknown

Dataset Information

0

The FGFR Family Inhibitor AZD4547 Exerts an Antitumor Effect in Ovarian Cancer Cells.


ABSTRACT: The dysregulation of fibroblast growth factor (FGF) signaling has been implicated in tumorigenesis, tumor progression, angiogenesis, and chemoresistance. The small-molecule AZD4547 is a potent inhibitor of FGF receptors. This study was performed to investigate the antitumor effects and determine the mechanistic details of AZD4547 in ovarian cancer cells. AZD4547 markedly inhibited the proliferation and increased the apoptosis of ovarian cancer cells. AZD4547 also suppressed the migration and invasion of ovarian cancer cells under nontoxic conditions. Furthermore, it attenuated the formation of spheroids and the self-renewal capacities of ovarian cancer stem cells and exerted an antiangiogenic effect. It also suppressed in vivo tumor growth in mice. Collectively, this study demonstrated the antitumor effect of AZD4547 in ovarian cancer cells and suggests that it is a promising agent for ovarian cancer therapy.

SUBMITTER: Na YR 

PROVIDER: S-EPMC8509426 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

The FGFR Family Inhibitor AZD4547 Exerts an Antitumor Effect in Ovarian Cancer Cells.

Na Yu Ran YR   Kim Jin Young JY   Song Chang Ho CH   Kim Mikyung M   Do Yen Thi YT   Vo Tam Thuy Lu TTL   Choi Eunsom E   Ha Eunyoung E   Seo Ji Hae JH   Shin So-Jin SJ  

International journal of molecular sciences 20211006 19


The dysregulation of fibroblast growth factor (FGF) signaling has been implicated in tumorigenesis, tumor progression, angiogenesis, and chemoresistance. The small-molecule AZD4547 is a potent inhibitor of FGF receptors. This study was performed to investigate the antitumor effects and determine the mechanistic details of AZD4547 in ovarian cancer cells. AZD4547 markedly inhibited the proliferation and increased the apoptosis of ovarian cancer cells. AZD4547 also suppressed the migration and inv  ...[more]

Similar Datasets

| S-EPMC4824600 | biostudies-literature
| S-EPMC9187670 | biostudies-literature
| S-EPMC10042809 | biostudies-literature
| S-EPMC5595825 | biostudies-literature
| S-EPMC6782013 | biostudies-literature
| S-EPMC6766871 | biostudies-literature
| S-EPMC6584658 | biostudies-literature
| S-EPMC7907049 | biostudies-literature
2024-11-17 | GSE267537 | GEO
| S-EPMC5546507 | biostudies-literature