Susan Lehman Cullman Laboratory for Cancer Research, Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.
Int J Mol Sci. 2024 Sep 21;25(18):10138. doi: 10.3390/ijms251810138.
The serine/threonine kinase PAK4 plays a crucial role in regulating cell proliferation, survival, migration, and invasion. Overexpression of PAK4 correlates with poor prognosis in some cancers. KPT-9274, a PAK4 inhibitor, significantly reduces the growth of triple-negative breast cancer cells and mammary tumors in mouse models, and it also inhibits the growth of several other types of cancer cells. Interestingly, although it was first identified as a PAK4 inhibitor, KPT-9274 was also found to inhibit the enzyme NAMPT (nicotinamide phosphoribosyltransferase), which is crucial for NAD (nicotinamide adenine dinucleotide) synthesis and vital for cellular energy and growth. These results made us question whether growth inhibition in response to KPT-9274 was due to PAK4 inhibition, NAMPT inhibition, or both. To address this, we tested several other PAK4 inhibitors that also inhibit cell growth, to determine whether they also inhibit NAMPT activity. Our findings confirm that multiple PAK4 inhibitors also inhibit NAMPT activity. This was assessed both in cell-free assays and in a breast cancer cell line. Molecular docking studies were also used to help us better understand the mechanism by which PAK4 inhibitors block PAK4 and NAMPT activity, and we identified specific residues on the PAK4 inhibitors that interact with NAMPT and PAK4. Our results suggest that PAK4 inhibitors may have a more complex mechanism of action than previously understood, necessitating further exploration of how they influence cancer cell growth.
丝氨酸/苏氨酸激酶 PAK4 在调节细胞增殖、存活、迁移和侵袭方面发挥着关键作用。PAK4 的过表达与一些癌症的不良预后相关。PAK4 抑制剂 KPT-9274 显著降低了三阴性乳腺癌细胞和小鼠模型中乳腺肿瘤的生长,并且还抑制了几种其他类型的癌细胞的生长。有趣的是,尽管它最初被鉴定为 PAK4 抑制剂,但 KPT-9274 也被发现抑制了酶 NAMPT(烟酰胺磷酸核糖基转移酶),该酶对 NAD(烟酰胺腺嘌呤二核苷酸)的合成至关重要,对细胞能量和生长也至关重要。这些结果使我们质疑对 KPT-9274 的生长抑制是否是由于 PAK4 抑制、NAMPT 抑制还是两者共同作用。为了解决这个问题,我们测试了几种其他也抑制细胞生长的 PAK4 抑制剂,以确定它们是否也抑制 NAMPT 活性。我们的研究结果证实,多种 PAK4 抑制剂也抑制 NAMPT 活性。这在无细胞测定和乳腺癌细胞系中都得到了评估。分子对接研究也被用于帮助我们更好地理解 PAK4 抑制剂阻断 PAK4 和 NAMPT 活性的机制,并且我们确定了 PAK4 抑制剂上与 NAMPT 和 PAK4 相互作用的特定残基。我们的研究结果表明,PAK4 抑制剂的作用机制可能比以前理解的更为复杂,需要进一步探索它们如何影响癌细胞的生长。