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

Sydney E Parks, Jason T Yustein
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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.

PAK1和PAK4作为尤文氏肉瘤治疗靶点的研究进展
尤文氏肉瘤(ES)是一种易发生转移的侵袭性儿童骨肿瘤。由于5年生存率低,转移性疾病的治疗选择有限,临床迫切需要改进ES治疗。靶向p21活化激酶(PAKs)可能是关键。PAK1和PAK4与侵袭性ES和不良患者预后相关,尽管它们在该疾病中的分子机制在很大程度上尚未明确。本评论旨在强调Qasim等人在“p21活化激酶作为治疗高风险Ewing肉瘤的可行治疗靶点”一文中对ES中PAK1和PAK4的理解的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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