Jiang Zhenming, Kong Chuize, Zhang Zhe, Zhu Yuyan, Zhang Yuxi, Chen Xi
Department of Urology, The First Affiliated Hospital of China Medical University, Shenyang, China.
J Cell Mol Med. 2015 May;19(5):1085-93. doi: 10.1111/jcmm.12503. Epub 2015 Mar 5.
In clinic, we examined the expression of protein kinase C (PKC)-α and Dicer in the samples of bladder cancer patients, and found that the two proteins have a line correlation. Our study confirmed this correlation existing by clearing the decreasing expression of Dicer after the PKC-α knockdown. Treatment of bladder cancer cell lines (T24, 5637) with the PKC-α or Dicer knockdown and the PKC inhibitors (Calphostin C and Gö 6976) can promote the apoptosis. Inhibition of PKC can increase the activities of caspase-3 and PARP, however, decrease the expression of Dicer. And knockdown of the PKC-α or Dicer can also activate the caspase-3 or the PARP. Considering the reduction of PKC-α can induce the Dicer down-regulation, we make the conclusion that the reduction of PKC-α can promote the apoptosis via the down-regulation of Dicer in bladder cancer.
在临床上,我们检测了膀胱癌患者样本中蛋白激酶C(PKC)-α和Dicer的表达,发现这两种蛋白呈线性相关。我们的研究通过清除PKC-α敲低后Dicer表达的降低证实了这种相关性的存在。用PKC-α或Dicer敲低以及PKC抑制剂(Calphostin C和Gö 6976)处理膀胱癌细胞系(T24、5637)可促进细胞凋亡。抑制PKC可增加caspase-3和PARP的活性,然而,会降低Dicer的表达。敲低PKC-α或Dicer也可激活caspase-3或PARP。考虑到PKC-α的降低可诱导Dicer下调,我们得出结论:PKC-α的降低可通过下调Dicer促进膀胱癌细胞凋亡。