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首页> 外文期刊>FEBS Open Bio >Anti-apoptotic role of peroxiredoxin III in cervical cancer cells ☆
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Anti-apoptotic role of peroxiredoxin III in cervical cancer cells ☆

机译:过氧化物酶毒素III在宫颈癌细胞中的抗凋亡作用☆

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As a member of peroxiredoxin (Prx) family, PrxIII is predominantly located in mitochondria and plays an important role as a scavenger of reactive oxygen species (ROS). Since previous reports demonstrated over-expression of PrxIII in cervical cancer, we conducted the present study to investigate the significance of PrxIII in cervical cancer development and/or progression.Cervical cancer cells were cultured from tissues derived from cervical cancer patients. After successful knockdown of PrxIII expression by small interfering RNA, we evaluated ROS level, viable cell number, and apoptosis of cervical cancer cells along with the culture time.The production of ROS was increased in cervical cancer cells as compared with normal cervical epithelia. Knockdown of PrxIII expression induced up-regulation of other Prx members including PrxI, PrxII, and PrxV. ROS level was higher in down-regulated cervical cancer cells than in controls and the difference was increasing with culture time. We also observed increased apoptosis and decreased viable cell number in down-regulated cervical cancer cells.Our results suggest that PrxIII is an indispensable ROS scavenger, which protects tumor cells against oxidative damage and subsequent apoptosis.Highlights? ROS production was increased in cervical cancer cells as compared with normal cervical epithelia. ? Knockdown of peroxiredoxin III (PrxIII) expression induced up-regulation of other Prx members. ? Down-regulation of PrxIII further increased ROS and subsequent apoptosis in cancer cells. ? PrxIII is an indispensable ROS scavenger and plays an important role in apoptotic inhibition.
机译:作为过氧化物酶(Prx)家族的成员,PrxIII主要位于线粒体中,并作为清除活性氧(ROS)的重要角色。由于先前的报道表明PrxIII在子宫颈癌中过表达,因此我们进行了本研究,以研究PrxIII在子宫颈癌的发展和/或进展中的意义。从子宫颈癌患者的组织中培养子宫颈癌细胞。通过小干扰RNA成功敲低PrxIII表达后,我们评估了ROS水平,存活细胞数和宫颈癌细胞的凋亡以及培养时间。与正常宫颈上皮细胞相比,宫颈癌细胞中ROS的产生增加了。抑制PrxIII表达可诱导其他Prx成员(包括PrxI,PrxII和PrxV)上调。下调的宫颈癌细胞中的ROS水平高于对照组,并且随着培养时间的增加而增加。我们还观察到在下调的宫颈癌细胞中凋亡增加,而活细胞数量减少。我们的结果表明PrxIII是必不可少的ROS清除剂,可保护肿瘤细胞免受氧化损伤和随后的凋亡。与正常宫颈上皮细胞相比,宫颈癌细胞中的ROS产量增加。 ?减少过氧化物酶III(PrxIII)表达诱导其他Prx成员的上调。 ? PrxIII的下调进一步增加了ROS和随后的癌细胞凋亡。 ? PrxIII是必不可少的ROS清除剂,并且在凋亡抑制中起重要作用。

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