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首页> 外文期刊>Minerva biotecnologica >Induction of apoptosis of human osteoclasts by the transcription factor decoy approach: relevance for the treatment of rheumatoid arthritis
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Induction of apoptosis of human osteoclasts by the transcription factor decoy approach: relevance for the treatment of rheumatoid arthritis

机译:转录因子诱饵方法诱导人破骨细胞凋亡:与类风湿关节炎的治疗相关性

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摘要

Rheumatoid arthritis (RA) is characterised by the presence of an inflammatory synovitis accompanied by destruction of joint cartilage and bone. Several evidences, both in vitro and hi animal models, indicate that osteoclasts (OCs) are key mediators of all forms of bone erosions and loss hi RA. Interestingly, transcription factor decoy (TFD) oligonucleotid.es targeting nuclear factor KB (NF-kB) are able to induce apoptosis of human primary OCs. This effect is associated with an increase of caspase-3 and a decrease of interleukin-6 production. Therefore, the effects of NF-kB decoys on OCs may be relevant for the development of treatments of RA. Accordingly, several evidences suggest apoptosis as a target for therapy of this inflammatory disease.
机译:类风湿关节炎(RA)的特征是存在炎性滑膜炎,伴有关节软骨和骨骼的破坏。体外和动物模型的一些证据表明,破骨细胞(OCs)是所有形式的骨侵蚀和RA丧失的关键介质。有趣的是,靶向核因子KB(NF-kB)的转录因子诱饵(TFD)寡核苷酸能够诱导人原代OC的凋亡。这种作用与caspase-3的增加和白介素6的产生减少有关。因此,NF-kB诱饵对OC的影响可能与RA治疗的发展有关。因此,一些证据表明凋亡是治疗该炎性疾病的靶标。

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