Sun S Y, Yue P, Shroot B, Hong W K, Lotan R
Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston 77030, USA.
Oncogene. 1999 Jul 1;18(26):3894-901. doi: 10.1038/sj.onc.1202771.
The novel synthetic retinoid 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid (CD437) has been recently identified to be a potent inducer of apoptosis in human non-small cell lung carcinoma (NSCLC) cells through a nuclear retinoic acid receptor independent mechanism. To approach the mechanism by which CD437 induces apoptosis in NSCLC cells, we investigated the involvement of c-Myc in CD437-induced apoptosis. CD437 (1 microM) up-regulated the expression of c-Myc and of its downstream target genes ornithine decarboxylase (ODC) and cdc25A in all three NSCLC cell lines (i.e., H460, SK-MES-1 and H1792) used. These effects were correlated with cellular susceptibilities to induction of apoptosis by CD437. Furthermore, CD437-induced apoptosis could be blocked by the ODC inhibitor difluoromethylornithine, the caspase inhibitors Z-VAD FMK and Z-DEVD FMK, and c-Myc antisense oligodeoxynucleotide, respectively. These data indicate that c-Myc gene plays an important role in mediating CD437-induced apoptosis in human NSCLC cells.
新型合成视黄酸6-[3-(1-金刚烷基)-4-羟基苯基]-2-萘甲酸(CD437)最近被确定为通过一种不依赖核视黄酸受体的机制,在人非小细胞肺癌(NSCLC)细胞中诱导凋亡的有效诱导剂。为了探究CD437在NSCLC细胞中诱导凋亡的机制,我们研究了c-Myc在CD437诱导凋亡中的作用。在所用的所有三种NSCLC细胞系(即H460、SK-MES-1和H1792)中,CD437(1 microM)上调了c-Myc及其下游靶基因鸟氨酸脱羧酶(ODC)和细胞周期蛋白依赖性激酶25A(cdc25A)的表达。这些效应与细胞对CD437诱导凋亡的敏感性相关。此外,CD437诱导的凋亡分别可被ODC抑制剂二氟甲基鸟氨酸、半胱天冬酶抑制剂Z-VAD FMK和Z-DEVD FMK以及c-Myc反义寡脱氧核苷酸阻断。这些数据表明,c-Myc基因在介导CD437诱导人NSCLC细胞凋亡中起重要作用。