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Commentary Open Access
Volume 2 | Issue 4 | DOI: https://doi.org/10.46439/cancerbiology.2.032

PAK1 and PAK4 as therapeutic targets for Ewing sarcoma: a commentary

  • 1Texas Children’s Cancer and Hematology Centers and The Faris D. Virani Ewing Sarcoma Center, Baylor College of Medicine, Houston, TX 77030, USA
  • 2Cancer and Cell Biology Program, Baylor College of Medicine, Houston, TX 77030, USA
  • 3Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA
  • 4Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA
+ Affiliations - Affiliations

Corresponding Author

Jason T. Yustein, yustein@bcm.edu

Received Date: September 02, 2021

Accepted Date: September 28, 2021

Abstract

Ewing sarcoma (ES) is an aggressive pediatric bone tumor that is prone to metastasis. Due to low five-year survival rates and limited therapeutic options for metastatic disease, there is a dire clinical need for improved ES treatments. Targeting p21-activated kinases (PAKs) may be key. PAK1 and PAK4 are associated with aggressive ES and poor patient outcomes, although their molecular mechanisms remain largely uncharacterized in this disease. This commentary aims to highlight the recent advancements made to the understanding of PAK1 and PAK4 in ES in the paper “p21-activated kinases as viable therapeutic targets for the treatment of high-risk Ewing sarcoma” by Qasim et al.

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