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首页> 外文期刊>FEBS Open Bio >Mycoplasma hyorhinis-encoded cytidine deaminase efficiently inactivates cytosine-based anticancer drugs
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Mycoplasma hyorhinis-encoded cytidine deaminase efficiently inactivates cytosine-based anticancer drugs

机译:支原体编码的胞苷脱氨酶可有效灭活基于胞嘧啶的抗癌药

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Mycoplasmas may colonize tumor tissue in patients. The cytostatic activity of gemcitabine was dramatically decreased in Mycoplasma hyorhinis-infected tumor cell cultures compared with non-infected tumor cell cultures. This mycoplasma-driven drug deamination could be prevented by exogenous administration of the cytidine deaminase (CDA) inhibitor tetrahydrouridine, but also by the natural nucleosides or by a purine nucleoside phosphorylase inhibitor. The M. hyorhinis-encoded CDA"H"y"o"r gene was cloned, expressed as a recombinant protein and purified. CDA"H"y"o"r was found to be more catalytically active than its human equivalent and efficiently deaminates (inactivates) cytosine-based anticancer drugs. CDA"H"y"o"r expression at the tumor site may result in selective drug inactivation and suboptimal therapeutic efficiency.
机译:支原体可能定植在患者的肿瘤组织中。与未感染的肿瘤细胞培养物相比,吉西他滨在支原体感染的肿瘤细胞培养物中的细胞抑制活性显着降低。可通过外源给予胞苷脱氨酶(CDA)抑制剂四氢尿苷来预防这种支原体驱动的药物脱氨反应,也可通过天然核苷或嘌呤核苷磷酸化酶抑制剂来预防。克隆了猪肺炎支原体编码的CDA“ H” y” o” r基因,表达为重组蛋白并纯化。发现CDA“ H” y“ o” r比其人类等效物更具催化活性,并有效地使基于胞嘧啶的抗癌药脱氨(失活)。在肿瘤部位的CDA“ H” y” o”表达可能导致选择性的药物失活和次佳的治疗效率。

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