Zhao Yan, Zhao Xiujuan, Yang Baofeng, Neuzil Jiri, Wu Kun
Department of Nutrition and Food, Harbin Medical University, Harbin, Heilongjiang Province, China.
Cancer Lett. 2007 Mar 18;247(2):345-52. doi: 10.1016/j.canlet.2006.05.015. Epub 2006 Jul 12.
Gastric neoplastic disease is one of the most frequent causes of cancer-associated deaths with poor prognosis. Here we studied the effect of the redox-silent analogue alpha-tocopheryl succinate (alpha-TOS), a strong apoptogen and anti-cancer agent, on the gastric cancer cell line SGC-7901. alpha-TOS inhibited proliferation of the cells and induced their apoptosis in a concentration- and time-dependent manner, while succinate or alpha-tocopherol showed no effect. The effect of alpha-TOS was modulated by components of the MAPK signaling network, including ERK1/2 and c-Jun N-terminal kinase (JNK), but not p38. Activation of ERK1/2 occurred early and increased until 12h, coinciding with an in crease in apoptosis in the cells, after which it dropped abruptly, while activation of JNK rose steadily, reaching a plateau at 12h of alpha-TOS treatment. The effects of ERK1/2 and JNK on the apoptosis outcome are transmitted via c-Jun, since transfection of the cells with c-Jun antisense oligodeoxynucleotide inhibited alpha-TOS-induced apoptosis. We conclude that ERK1/2 and JNK positively regulate apoptosis induced in gastric cancer cells by alpha-TOS.
胃癌性疾病是癌症相关死亡的最常见原因之一,预后较差。在此,我们研究了氧化还原沉默类似物琥珀酸生育酚(α-TOS),一种强效凋亡原和抗癌剂,对胃癌细胞系SGC-7901的影响。α-TOS以浓度和时间依赖性方式抑制细胞增殖并诱导其凋亡,而琥珀酸或生育酚则无此作用。α-TOS的作用受丝裂原活化蛋白激酶(MAPK)信号网络成分的调节,包括细胞外信号调节激酶1/2(ERK1/2)和c-Jun氨基末端激酶(JNK),但不受p38的调节。ERK1/2的激活发生较早,并持续增加至12小时,这与细胞凋亡增加相吻合,之后其突然下降,而JNK的激活则稳步上升,在α-TOS处理12小时时达到平台期。ERK1/2和JNK对凋亡结果的影响通过c-Jun传递,因为用c-Jun反义寡脱氧核苷酸转染细胞可抑制α-TOS诱导的凋亡。我们得出结论,ERK1/2和JNK正向调节α-TOS诱导的胃癌细胞凋亡。