
As tumor angiogenesis is one of the hallmarks of cancer, the inhibition of vascular endothelial growth factor signaling has become an attractive anticancer approach. Apatinib, a small-molecule inhibitor of vascular endothelial growth factor receptor-2, has demonstrated encouraging anticancer activity across a broad range of malignancies, including gastric cancer, non-small-cell lung cancer, breast cancer, and hepatocellular carcinoma. In this up-to-date review, focus is not only on the structure, mechanisms, and pharmacokinetics of apatinib, but also on summarizing clinical trials and making recommendations of apatinib for patients with advanced solid tumors.
Drug Design, Development and Therapy, Molecular Structure, Neovascularization, Pathologic, Pyridines, Angiogenesis Inhibitors, RM1-950, Review, Vascular Endothelial Growth Factor Receptor-2, Treatment Outcome, Neoplasms, Animals, Humans, Therapeutics. Pharmacology, Molecular Targeted Therapy, Signal Transduction
Drug Design, Development and Therapy, Molecular Structure, Neovascularization, Pathologic, Pyridines, Angiogenesis Inhibitors, RM1-950, Review, Vascular Endothelial Growth Factor Receptor-2, Treatment Outcome, Neoplasms, Animals, Humans, Therapeutics. Pharmacology, Molecular Targeted Therapy, Signal Transduction
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 189 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 1% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 1% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
