Key Laboratory of Tumor Molecular Biology in Binzhou Medical University, Department of Biochemistry and Molecular Biology, Binzhou Medical University, YanTai, ShanDong 264003, PR China; The Key Laboratory of Traditional Chinese Medicine Prescription Effect and Clinical Evaluation of State Administration of Traditional Chinese Medicine, School of Pharmacy, Binzhou Medical University, YanTai, ShanDong 264003, PR China.
Yantai Institute of Coastal Zone Research Chinese Academy of Sciences, Yantai 264003, PR China.
Free Radic Biol Med. 2018 Dec;129:177-185. doi: 10.1016/j.freeradbiomed.2018.09.016. Epub 2018 Sep 15.
Previous studies have confirmed that protein tyrosine phosphatase 1B (PTP1B) can promote tumour progression in non-small cell lung cancer (NSCLC). Vanadyl alginate oligosaccharides (VAOS) is a new coordination compounds that possesses a good PTP1B inhibitory activity. However, the potent anticancer efficacy of VAOS in human NSCLC requires further study. In this study, VAOS exhibited effective inhibitory effects in NSCLC both in cultured cells and in a xenograft mouse model. VAOS was further identified to induce NSCLC cell apoptosis through activating protein kinase B (AKT) to elevate intracellular reactive oxygen species (ROS) levels by increasing in oxygen consumption and impairing the ROS-scavenging system. Neither silencing of PTP1B by siRNA nor transient overexpression of PTP1B had an effect on the AKT phosphorylation triggered by VAOS, indicating that PTP1B inhibition was not involved in VAOS-induced apoptosis. Through phosphorus colorimetric assay, we demonstrated that VAOS notably inhibited phosphatase and tensin homologue deleted on chromosome 10 (PTEN) dephosphorylation activity, another member of the protein tyrosine phosphatases (PTPases)-upstream factor of AKT. Interestingly, PTEN knockdown sensitized cells to VAOS, whereas ectopic expression of PTEN markedly rescued VAOS-mediated lethality. In vivo, VAOS treatment markedly reduced PTEN activity and tumour cell burden with low systemic toxicity. Thus, our data not only provided a new therapeutic drug candidate for NSCLC, but presented new understanding into the pharmacological research of VAOS.
先前的研究已经证实,蛋白酪氨酸磷酸酶 1B(PTP1B)可以促进非小细胞肺癌(NSCLC)的肿瘤进展。海藻酸钠寡糖钒(VAOS)是一种新的配位化合物,具有良好的 PTP1B 抑制活性。然而,VAOS 在人 NSCLC 中的强大抗癌疗效需要进一步研究。在这项研究中,VAOS 在培养的细胞和异种移植小鼠模型中均显示出对 NSCLC 的有效抑制作用。VAOS 进一步被鉴定为通过激活蛋白激酶 B(AKT)来诱导 NSCLC 细胞凋亡,通过增加耗氧量和损害 ROS 清除系统来提高细胞内活性氧(ROS)水平。用 siRNA 沉默 PTP1B 或瞬时过表达 PTP1B 均对 VAOS 触发的 AKT 磷酸化没有影响,这表明 PTP1B 抑制不参与 VAOS 诱导的细胞凋亡。通过磷比色法测定,我们证明 VAOS 显著抑制了磷酸酶和张力蛋白同源物缺失于染色体 10(PTEN)的去磷酸化活性,AKT 的另一个蛋白酪氨酸磷酸酶(PTPases)-上游因子。有趣的是,PTEN 敲低使细胞对 VAOS 敏感,而外源性表达 PTEN 则显著挽救了 VAOS 介导的致死性。在体内,VAOS 处理显著降低了 PTEN 活性和肿瘤细胞负荷,同时具有低系统毒性。因此,我们的数据不仅为 NSCLC 提供了一种新的治疗药物候选物,还为 VAOS 的药理学研究提供了新的认识。