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首页> 外文期刊>Journal of neuro-oncology. >Brain derived neurotrophic factor protects human neuroblastoma cells from DNA damaging agents.
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Brain derived neurotrophic factor protects human neuroblastoma cells from DNA damaging agents.

机译:脑源性神经营养因子可保护人类神经母细胞瘤细胞免受DNA破坏剂的侵害。

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摘要

Neurotrophins are required for survival of neurons during development and may act as survival factors to cells undergoing stress. We tested whether brain derived neurotrophic factor (BDNF) protects neuroblastoma (NB) cells from cytotoxic agents using a model NB cell line, NB 1643, which expresses functional tropomyosin related kinase B (TRKB) following treatment with all-trans-retinoic acid. TRKB is the receptor for BDNF. BDNF increases the EC50 values in survival assays for cisplatin, doxorubicin, and topotecan by two to three fold. Thus, BDNF does indeed protect cells drugs that damage DNA. Cisplatin and doxorubicin are used to treat NB. Topotecan is in clinical studies for the treatment of NB. Since these drugs induce DNA damage, we also investigated whether BDNF might afford protection from gamma irradiation. BDNF also induces more than a two fold resistance to gamma irradiation. Since BDNF protects cells from agents with different mechanisms of damaging DNA and resistance, it seems likely that BDNF may alter a common signaling pathway required for cell death initiation by DNA damaging agents.
机译:神经营养蛋白是发育过程中神经元生存所必需的,并且可能是承受压力的细胞的生存因子。我们使用模型NB细胞系NB 1643测试了脑源性神经营养因子(BDNF)是否能保护神经母细胞瘤(NB)细胞免受细胞毒性剂的侵害,该细胞系在用全反式维甲酸处理后表达功能性原肌球蛋白相关激酶B(TRKB)。 TRKB是BDNF的受体。 BDNF将生存率测定中的顺铂,阿霉素和托泊替康的EC50值提高了2到3倍。因此,BDNF确实可以保护破坏DNA的细胞药物。顺铂和阿霉素用于治疗NB。托泊替康正在临床治疗NB中。由于这些药物会诱导DNA损伤,因此我们还研究了BDNF是否可以提供伽玛射线的保护。 BDNF对伽玛射线的诱导也超过两倍。由于BDNF保护细胞免受具有破坏DNA和抗药性的机制不同的作用,因此BDNF可能会改变DNA破坏剂引发细胞死亡所需的常见信号通路。

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