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Discovery of a Potential HER2 Inhibitor from Natural Products for the Treatment of HER2-Positive Breast Cancer.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2016 Jul 01; Vol. 17 (7). Date of Electronic Publication: 2016 Jul 01. - Publication Year :
- 2016
-
Abstract
- Breast cancer is one of the most lethal types of cancer in women worldwide due to the late stage detection and resistance to traditional chemotherapy. The human epidermal growth factor receptor 2 (HER2) is considered as a validated target in breast cancer therapy. Even though a substantial effort has been made to develop HER2 inhibitors, only lapatinib has been approved by the U.S. Food and Drug Administration (FDA). Side effects were observed in a majority of the patients within one year of treatment initiation. Here, we took advantage of bioinformatics tools to identify novel effective HER2 inhibitors. The structure-based virtual screening combined with ADMET (absorption, distribution, metabolism, excretion and toxicity) prediction was explored. In total, 11,247 natural compounds were screened. The top hits were evaluated by an in vitro HER2 kinase inhibition assay. The cell proliferation inhibition effect of identified inhibitors was evaluated in HER2-overexpressing SKBR3 and BT474 cell lines. We found that ZINC15122021 showed favorable ADMET properties and attained high binding affinity against HER2. Moreover, ZINC15122021 showed high kinase inhibition activity against HER2 and presented outstanding cell proliferation inhibition activity against both SKBR3 and BT474 cell lines. Results reveal that ZINC15122021 can be a potential HER2 inhibitor.
- Subjects :
- Acetanilides metabolism
Acetanilides pharmacokinetics
Acetanilides pharmacology
Area Under Curve
Binding Sites
Biological Products metabolism
Biological Products pharmacokinetics
Breast Neoplasms metabolism
Breast Neoplasms pathology
Cell Line, Tumor
Cell Survival drug effects
Female
Half-Life
Humans
Lapatinib
Molecular Docking Simulation
Protein Kinase Inhibitors pharmacokinetics
Protein Kinase Inhibitors pharmacology
Protein Structure, Tertiary
Quinazolines metabolism
Quinazolines pharmacokinetics
ROC Curve
Receptor, ErbB-2 metabolism
Thiazolidinediones metabolism
Thiazolidinediones pharmacokinetics
Thiazolidinediones pharmacology
Biological Products pharmacology
Cell Proliferation drug effects
Receptor, ErbB-2 antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 17
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 27376283
- Full Text :
- https://doi.org/10.3390/ijms17071055