Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 Mar;14(3):183-202.
doi: 10.1038/nrd4534. Epub 2015 Feb 20.

Unleashing the therapeutic potential of human kallikrein-related serine proteases

Affiliations
Review

Unleashing the therapeutic potential of human kallikrein-related serine proteases

Ioannis Prassas et al. Nat Rev Drug Discov. 2015 Mar.

Erratum in

  • Nat Rev Drug Discov. 2015 Oct;14(10):732

Abstract

Tissue kallikreins are a family of fifteen secreted serine proteases encoded by the largest protease gene cluster in the human genome. In the past decade, substantial progress has been made in characterizing the natural substrates, endogenous inhibitors and in vivo functions of kallikreins, and studies have delineated important pathophysiological roles for these proteases in a variety of tissues. Thus, kallikreins are now considered attractive targets for the development of novel therapeutics for airway, cardiovascular, tooth, brain, skin and neoplastic diseases. In this Review, we discuss recent advances in our understanding of the physiological functions and pathological implications of kallikrein proteases, and highlight progress in the identification of kallikrein inhibitors, which together are bringing us closer to therapeutically targeting kallikreins in selected disease settings.

PubMed Disclaimer

References

    1. Clin Genitourin Cancer. 2010 Dec 1;8(1):10-6 - PubMed
    1. Int Arch Allergy Immunol. 2008;147(4):299-304 - PubMed
    1. Neurosci Lett. 2006 Sep 25;405(3):175-80 - PubMed
    1. Am J Physiol Cell Physiol. 2012 Nov 1;303(9):C936-46 - PubMed
    1. Eur J Neurosci. 2000 Apr;12(4):1479-86 - PubMed

Publication types

MeSH terms

LinkOut - more resources