Freeman Ruth E, Neuzil Jiri
Apoptosis Research Group, Heart Foundation Research Centre, School of Medical Science, Griffith University, Southport, Qld 9716, Australia.
FEBS Lett. 2006 May 15;580(11):2671-6. doi: 10.1016/j.febslet.2006.04.019. Epub 2006 Apr 21.
Malignant mesothelioma (MM) is a fatal type of cancer. We studied the role of the redox-active protein thioredoxin-1 (Trx-1) in apoptosis induced in MM cells and their non-malignant counterparts (Met-5A) by alpha-tocopheryl succinate (alpha-TOS) and TNF-related apoptosis-inducing ligand (TRAIL). MM cells were susceptible to alpha-TOS and less to TRAIL, while Met-5A cells were susceptible to TRAIL and resistant to alpha-TOS. MM cells expressed very low level of the Trx-1 protein, which was high in Met-5A cells, while the level of Trx-1 mRNA was similar in all cell lines. Downregulation of Trx-1 further sensitised Met-5A cells to TRAIL but not to alpha-TOS. Our data suggest that the role of Trx-1 in apoptosis modulation is unrelated to its anti-oxidant properties.
恶性间皮瘤(MM)是一种致命的癌症类型。我们研究了氧化还原活性蛋白硫氧还蛋白-1(Trx-1)在α-生育酚琥珀酸酯(α-TOS)和肿瘤坏死因子相关凋亡诱导配体(TRAIL)诱导MM细胞及其非恶性对应物(Met-5A)凋亡中的作用。MM细胞对α-TOS敏感,对TRAIL不敏感,而Met-5A细胞对TRAIL敏感,对α-TOS有抗性。MM细胞中Trx-1蛋白表达水平极低,在Met-5A细胞中则很高,而Trx-1 mRNA水平在所有细胞系中相似。Trx-1的下调进一步使Met-5A细胞对TRAIL敏感,但对α-TOS不敏感。我们的数据表明,Trx-1在凋亡调节中的作用与其抗氧化特性无关。