Robert H. Lurie Comprehensive Cancer Center, Division of Hematology-Oncology, Northwestern University, Medical School, Jesse Brown VA Medical Center, Chicago, IL 60611, USA.
Biochem Biophys Res Commun. 2010 Jul 16;398(1):135-9. doi: 10.1016/j.bbrc.2010.06.052. Epub 2010 Jun 17.
Extensive studies over the years have shown that the AMP-activated kinase (AMPK) exhibits negative regulatory effects on the activation of the mammalian target of rapamycin (mTOR) signaling cascade. We examined the potential involvement of AMPK in the regulation of growth and survival of malignant melanoma cells. In studies using the AMPK activators AICAR or metformin, we found potent inhibitory effects of AMPK activity on the growth of SK-MEL-2 and SK-MEL-28 malignant melanoma cells. Induction of AMPK activity was also associated with inhibition of the ability of melanoma cells to form colonies in an anchorage-independent manner in soft agar, suggesting an important role of the pathway in the control of malignant melanoma tumorigenesis. Furthermore, AICAR-treatment resulted in malignant melanoma cell death and such induction of apoptosis was further enhanced by concomitant statin-treatment. Taken together, our results provide evidence for potent inhibitory effects of AMPK on malignant melanoma cell growth and survival and raise the potential of AMPK manipulation as a novel future approach for the treatment of malignant melanoma.
多年来的广泛研究表明,AMP 激活的蛋白激酶 (AMPK) 对哺乳动物雷帕霉素靶蛋白 (mTOR) 信号级联的激活表现出负向调节作用。我们研究了 AMPK 是否参与调节恶性黑素瘤细胞的生长和存活。在使用 AMPK 激活剂 AICAR 或二甲双胍的研究中,我们发现 AMPK 活性对 SK-MEL-2 和 SK-MEL-28 恶性黑素瘤细胞的生长具有强烈的抑制作用。AMPK 活性的诱导也与抑制黑素瘤细胞在软琼脂中以非锚定方式形成集落的能力有关,这表明该途径在控制恶性黑素瘤肿瘤发生中起着重要作用。此外,AICAR 处理导致恶性黑素瘤细胞死亡,并且这种细胞凋亡的诱导通过伴随的他汀类药物处理进一步增强。总之,我们的结果提供了 AMPK 对恶性黑素瘤细胞生长和存活的强烈抑制作用的证据,并提出了操纵 AMPK 的可能性,作为治疗恶性黑素瘤的一种新的未来方法。