Promising novel therapeutic targets for kidney disease: Emphasis on kidney-specific proteins
Drug Discovery Today, ISSN: 1359-6446, Vol: 28, Issue: 2, Page: 103466
2023
- 5Citations
- 21Captures
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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
- Citations5
- Citation Indexes5
- Captures21
- Readers21
- 21
Review Description
Worldwide, around 850 million people are diagnosed with kidney disease but the available treatment options are still limited. Preclinical studies propose a plethora of druggable targets that can attenuate kidney disease and could qualify as novel therapeutic strategies, although most of these targets still await clinical testing. Here, we review some promising candidate targets for chronic kidney disease: intermedin, periostin, sirtuin, the cannabinoid receptor, Klotho, and uromodulin. For acute kidney injury, we discuss Apelin, Elabela, growth differentiation factor-15, Fyn kinase, and Klotho. Target selection for further clinical development should consider redundancies with the standard of care, potential synergistic effects with existing treatments, as well as the potential of additional effects on the cardiovascular system as a common comorbidity in patients with kidney disease.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1359644622004597; http://dx.doi.org/10.1016/j.drudis.2022.103466; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85145602113&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/36509391; https://linkinghub.elsevier.com/retrieve/pii/S1359644622004597; https://dx.doi.org/10.1016/j.drudis.2022.103466
Elsevier BV
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