Advances in the development of Rho GTPase inhibitors
Bioorganic & Medicinal Chemistry, ISSN: 0968-0896, Vol: 90, Page: 117337
2023
- 8Citations
- 9Captures
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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
- Citations8
- Citation Indexes8
- CrossRef2
- Captures9
- Readers9
Review Description
Rho guanosine triphosphatases (Rho GTPases), as members of the Ras superfamily, are GDP/GTP binding proteins that behave as molecular switches for the transduction of signals from external stimuli. Rho GTPases play essential roles in a number of cellular processes including cell cycle, cell polarity as well as cell migration. The dysregulations of Rho GTPases are related with various diseases, especially with cancers. Accumulating evidence supports that Rho GTPases play important roles in cancer development and progression. Rho GTPases become potential therapeutic targets for cancer therapy. And a number of inhibitors targeting Rho GTPases have been developed. In this review, we discuss their structural features, summarize their roles in cancer, and focus on the recent progress of their inhibitors, which are beneficial for the drug discovery targeting Rho GTPases.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0968089623001852; http://dx.doi.org/10.1016/j.bmc.2023.117337; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85160323884&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37253305; https://linkinghub.elsevier.com/retrieve/pii/S0968089623001852; https://dx.doi.org/10.1016/j.bmc.2023.117337
Elsevier BV
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