The anti-tumor activity and molecular mechanisms of an Aurora kinase inhibitor ZLJ213 in suppressing colon cancer growth / 药学学报
Yao Xue Xue Bao
; (12): 854-860, 2015.
Article
in Zh
| WPRIM
| ID: wpr-257056
Responsible library:
WPRO
ABSTRACT
The aim of this study is to evaluate anti-tumor activities and mechanism of a novel kinase inhibitor ZLJ213 which targeted Aurora A and vascular endothelial growth factor receptor (VEGFR) in vitro and in vivo against human colon cancer. Results showed that ZLJ213 inhibited cell proliferation and induced cell cycle arrest and apoptosis of HCT1 16 and SW48 cell lines. In HCT116-derived xenograft, ZLJ213 dosed at 100 mg · kg(-1) inhibited tumor growth by 73.24%. The IC50 of ZLJ213 on the expression of p-Aurora A was 0.258 µmol · L(-1) analyzed by ELISA. Under the concentration of 0.08 µmol · L(-1), ZLJ213 could inhibit the activities of Aurora A, Histone H3 and VEGFR of HCT116 and SW48 cell lines. Simultaneously, ZLJ213 induced activation of Caspase 3 and PARP cleavage. Above data suggested that ZLJ213 had the ability to inhibit cell proliferation and induce cell apoptosis both in vitro and in vivo in colon cancer, and down-regulate the expression of p-Aurora A and p-VEGFR. ZLJ213 might be a potential therapeutic agent against colon cancer.
Full text:
1
Database:
WPRIM
Main subject:
Pathology
/
Pharmacology
/
Apoptosis
/
Colonic Neoplasms
/
Xenograft Model Antitumor Assays
/
Receptors, Vascular Endothelial Growth Factor
/
Cell Line, Tumor
/
Protein Kinase Inhibitors
/
Cell Proliferation
/
Cell Cycle Checkpoints
Type of study:
Prognostic_studies
Limits:
Animals
/
Humans
Language:
Zh
Journal:
Yao Xue Xue Bao
Year:
2015
Document type:
Article