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
. 2008 Jun;12(6):757-67.
doi: 10.1517/14728222.12.6.757.

Src inhibitors in breast cancer therapy

Affiliations
Review

Src inhibitors in breast cancer therapy

Stephen Hiscox et al. Expert Opin Ther Targets. 2008 Jun.

Abstract

Background: Recent evidence has established the non receptor tyrosine kinase, Src, as a critical component of multiple signalling pathways that regulate proliferation, survival, angiogenesis and metastasis. Increased levels of Src protein and activity are widely reported in human cancers including breast cancer, and its important role in oncogenic processes makes it a potential target for therapeutic intervention.

Objective: To review the role of Src kinase in breast cancer and discuss its potential as a therapeutic target.

Methods: Literature citing preclinical and clinical studies with Src inhibitors was reviewed.

Conclusion: Experimental data with small-molecule inhibitors of Src kinase in breast cancer are encouraging, demonstrating effective suppression in vitro of tumour growth and invasion and inhibition of disease spread in preclinical models in vivo. Recently several Src inhibitors have been tested in Phase I clinical trials where they are well tolerated and demonstrate low toxicity. Overall, these findings suggest that Src inhibitors present a future therapeutic option in the treatment of breast cancer growth and progression.

PubMed Disclaimer

Publication types

MeSH terms

LinkOut - more resources