Therapeutic potentials of Apatinib in cancer treatment: Possible mechanisms and clinical relevance
Life Sciences, ISSN: 0024-3205, Vol: 241, Page: 117106
2020
- 75Citations
- 43Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations75
- Citation Indexes75
- 75
- CrossRef40
- Captures43
- Readers43
- 43
Review Description
Metastasis is one of the main issues in cancer treatment and it has been documented that angiogenesis plays an important role in this process. Studies showed that vascular endothelial growth factor (VEGF) and its receptor (VEGFR) have elevated expression in tumors and are involved in tumor progression and metastasis; suggesting their potential for being a therapeutic target. In this regard, Apatinib or YN968D1, a specific inhibitor of VEGFR-2 has been suggested as a promising therapeutic agent for cancer that can prevent tumor angiogenesis and metastasis. Furthermore, this drug can sensitize resistant tumor cells to chemotherapy drugs and increase the effectiveness of conventional chemotherapy drugs. Recent studies have shown that Apatinib has beneficial implications as a post-second and third-line therapy agent in a variety of cancers. Furthermore, Apatinib has the capacity to promote the overall survival and progression-free survival of cancer patients. This review discussed about, the molecular mechanisms and clinical relevance underlying the therapeutic potential of Apatinib in cancer treatment.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0024320519310331; http://dx.doi.org/10.1016/j.lfs.2019.117106; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85076113361&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/31786193; https://linkinghub.elsevier.com/retrieve/pii/S0024320519310331; https://dx.doi.org/10.1016/j.lfs.2019.117106
Elsevier BV
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