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新型钒化合物 Van-7 的 DNA 结合和拓扑异构酶 I 抑制活性。

DNA-Binding and Topoisomerase-I-Suppressing Activities of Novel Vanadium Compound Van-7.

机构信息

Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, 5 Yu-Shan Road, Qingdao 266003, China ; The Department of Pharmacy, Qingdao Women and Children Hospital, 127 Liao-Yang West Road, Qingdao 266034, China.

出版信息

Bioinorg Chem Appl. 2012;2012:756374. doi: 10.1155/2012/756374. Epub 2012 Sep 30.

Abstract

Vanadium compounds were studied during recent years to be considered as a representative of a new class of nonplatinum metal anticancer agents in combination to its low toxicity. Here, we found a vanadium compound Van-7 as an inhibitor of Topo I other than Topo II using topoisomerase-mediated supercoiled DNA relaxation assay. Agarose gel electrophoresis and comet assay showed that Van-7 treatment did not produce cleavable complexes like HCPT, thereby suggesting that Topo I inhibition occurred upstream of the relegation step. Further studies revealed that Van-7 inhibited Topo I DNA binding involved in its intercalating DNA. Van-7 did not affect the catalytic activity of DNase I even up to100 μM. Van-7 significantly suppressed the growth of cancer cell lines with IC(50) at nanomolar concentrations and arrested cell cycle of A549 cells at G2/M phase. All these results indicate that Van-7 is a potential selective Topo I inhibitor with anticancer activities as a kind of Topo I suppressor, not Topo I poison.

摘要

近年来,人们研究了钒化合物,因为它具有低毒性,所以被认为是一种新型非铂类金属抗癌药物。在这里,我们发现了一种名为 Van-7 的钒化合物,它是拓扑异构酶介导的超螺旋松弛测定法中的拓扑异构酶 I 的抑制剂,而非拓扑异构酶 II 的抑制剂。琼脂糖凝胶电泳和彗星实验表明,Van-7 处理不会产生像 HCPT 那样的可切割复合物,从而表明拓扑异构酶 I 抑制发生在分离步骤之前。进一步的研究表明,Van-7 抑制拓扑异构酶 I 与它嵌入 DNA 相关的 DNA 结合。Van-7 甚至在高达 100μM 的浓度下也不会影响 DNA 酶 I 的催化活性。Van-7 能显著抑制具有纳摩尔浓度 IC50 的癌细胞系的生长,并将 A549 细胞的细胞周期阻滞在 G2/M 期。所有这些结果表明,Van-7 是一种潜在的选择性拓扑异构酶 I 抑制剂,具有抗癌活性,作为一种拓扑异构酶 I 抑制剂,而不是拓扑异构酶 I 毒物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d82a/3465879/914bb24715f7/BCA2012-756374.001.jpg

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