Department of Cell Biology, China Medical University, Key Laboratory of Cell Biology, Ministry of Public Health, Shenyang, Liaoning 110001, P. R. China.
Expert Opin Ther Targets. 2010 Apr;14(4):419-33. doi: 10.1517/14728221003642019.
Gastric cancer is one of the most common causes of cancer death worldwide. P21-activated kinases (PAKs), regulators of cancer-cell signalling networks, play fundamental roles in a range of cellular processes through their binding partners or kinase substrates.
The complex regulation of PAKs through their upstream or downstream effectors in human cancers, especially in gastric cancer, are described and the identified inhibitors of PAKs are summarized.
The structural differences and activation mechanisms between two subgroups of PAK are described. Both groups of PAKs play complicated and important roles in human gastric cancer, which indicated a possible way for us to identify the specific inhibitors targeting PAKs for gastric cancer.
PAKs play important roles in progression of many cancer types, the full mechanisms of PAKs in gastric cancer are still unclear. It seems there are different roles for two groups of PAKs in cancers. Group I PAKs play their functions mostly through their specific substrates, however, many binding partners that are independent of phosphorylation by group II PAKs were identified. Finding specific inhibitors of PAKs will help us discover the roles of PAKs and target these kinases in human gastric cancer.
胃癌是全球癌症死亡的最常见原因之一。P21 激活激酶(PAKs)是癌细胞信号网络的调节剂,通过其结合伴侣或激酶底物,在一系列细胞过程中发挥着基本作用。
描述了 PAK 在人类癌症中的上游或下游效应物的复杂调节,特别是在胃癌中,并总结了已鉴定的 PAK 抑制剂。
描述了 PAK 两个亚群之间的结构差异和激活机制。两组 PAK 在人类胃癌中发挥着复杂而重要的作用,这为我们识别针对 PAK 的特异性抑制剂以治疗胃癌提供了可能的途径。
PAKs 在许多癌症类型的进展中发挥重要作用,PAKs 在胃癌中的完整机制尚不清楚。两组 PAK 在癌症中似乎发挥着不同的作用。I 组 PAK 主要通过其特定的底物发挥功能,然而,已经鉴定出许多与 II 组 PAK 的磷酸化无关的结合伴侣。寻找 PAK 的特异性抑制剂将有助于我们发现 PAK 的作用,并将这些激酶作为靶点用于人类胃癌的治疗。