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c-Jun knockdown sensitizes osteosarcoma to doxorubicin.

机译:c-Jun抑制使骨肉瘤对阿霉素敏感。

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摘要

The oncogene c-Jun has been found to be up-regulated in a variety of cancers, including osteosarcoma. Doxorubicin is a frontline chemotherapeutic against osteosarcoma, but is limited by toxicity. DNAzymes are oligonucleotides capable of specific catalysis of target mRNA. A biocompatible c-Jun DNAzyme nanoparticle formulated from chitosan regressed the growth and metastasis of pre-established tumors, especially in combination with doxorubicin. In vitro data confirmed that c-Jun knockdown chemosensitized these cells to doxorubicin treatment. c-Jun down-regulation-mediated tumor inhibition also led to concomitant decreased osteolysis. Clinically, knockdown of c-Jun with chitosan nanobiotechnology may proffer an improved treatment outcome for osteosarcoma.
机译:已发现癌基因c-Jun在包括骨肉瘤在内的多种癌症中被上调。阿霉素是针对骨肉瘤的一线化疗药物,但受到毒性的限制。 DNA核酶是能够特异性催化靶mRNA的寡核苷酸。由壳聚糖配制的具有生物相容性的c-Jun DNAzyme纳米粒子可逆转预先建立的肿瘤的生长和转移,特别是与阿霉素联用时。体外数据证实,c-Jun敲低可使这些细胞对阿霉素治疗产生化学敏感性。 c-Jun下调介导的肿瘤抑制作用还导致骨溶解减少。在临床上,用壳聚糖纳米生物技术敲除c-Jun可能会改善骨肉瘤的治疗效果。

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