Skip to content
2000
Volume 7, Issue 6
  • ISSN: 1871-5206
  • E-ISSN: 1875-5992

Abstract

Targeting Bruton's tyrosine kinase (BTK) with a small molecule inhibitor may be useful in treatment of BTK-expressing malignancies because of the anti-apoptotic function of BTK in cancer cells. Furthermore, BTK inhibitors also exhibit anti-thrombotic properties that may be desirable in the context of the increased risk of thromboembolic complications in cancer patients. This review will focus on the role of BTK in drug resistance in cancer, thromboembolism, and various pathologic immune responses, such as graft versus host disease. The therapeutic potential of targeting BTK is illustrated by discussion of the biologic activity profile of the rationally designed BTK inhibitor LFM-A13.

Loading

Article metrics loading...

/content/journals/acamc/10.2174/187152007784111331
2007-11-01
2025-04-01
Loading full text...

Full text loading...

/content/journals/acamc/10.2174/187152007784111331
Loading

  • Article Type:
    Research Article
Keyword(s): BTK; cancer; Rational drug design; thromboembolism; tyrosine kinases
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test