| 靶向抑制拓扑异构酶和端粒酶的钌配合物研究进展 |
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| 引用本文： | 陈相,巢晖,计亮年. 靶向抑制拓扑异构酶和端粒酶的钌配合物研究进展[J]. 无机化学学报, 2013, 29(18) |
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| 作者姓名： | 陈相 巢晖 计亮年 |
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| 作者单位： | 中山大学化学与化学工程学院生物无机与合成化学教育部重点实验室, 广州 510275,中山大学化学与化学工程学院生物无机与合成化学教育部重点实验室, 广州 510275,中山大学化学与化学工程学院生物无机与合成化学教育部重点实验室, 广州 510275 |
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| 基金项目： | 973项目(No.2015CB85630)、国家自然科学基金(Nos.21172273,21171177,21471164)和教育部高校博士点基金博导类课题(No.20110171110013)资助项目。 |
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| 摘 要： | 金属配合物抗肿瘤研究,尤其是铂类药物,已取得了相对令人瞩目的成功,但同时也面临着包括耐药性和毒副作用等诸多问题。近年来钌配合物作为新的抗癌药物引起了人们的注意。在非铂系药物中,金钌配合物;拓扑异构酶;G-四链体;端粒酶属钌配合物是最有前途的抗癌药物之一,国际上普遍认为钌和钌的配合物属于低毒性,容易吸收并在体内很快排泄。本文将着重介绍钌配合物与DNA结合后进一步引发的细胞内核酶活性抑制研究,从新的角度来诠释钌配合物的抗肿瘤研究最新进展。
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| 关 键 词： | 钌配合物 拓扑异构酶 G-四链体 端粒酶 |
New Trends of Ruthenium Complexes as Inhibitors Targeting Topoisomerase and Telomerase |
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| CHEN Xiang,CHAO Hui and JI Liang-Nian. New Trends of Ruthenium Complexes as Inhibitors Targeting Topoisomerase and Telomerase[J]. Chinese Journal of Inorganic Chemistry, 2013, 29(18) |
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| Authors: | CHEN Xiang CHAO Hui JI Liang-Nian |
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| Affiliation: | MOE Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China,MOE Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China and MOE Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China |
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| Abstract: | The anti-tumor study of metal complexes, especially the platinum-base drugs, has achieved remarkable success but still facing several problems such as drugs resistance and side effects. Recently, ruthenium complexes attract many scientists' interests with their brand new application of anti-tumor drugs. In the series of non-platinum drugs, ruthenium complexes are regarded as one of the most potential anti-tumor drugs for the reason not merely the metal ruthenium and its complexes exhibit low toxicity but also they can be efficiently absorbed and excreted for human body. Herein, the study of the follow-up inhibition towards nucleus enzymes induced by the binding between ruthenium complexes and DNA was expatiated, introducing the advance anti-tumor applications of ruthenium complexes in new perspectives. |
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| Keywords: | ruthenium complexes topoisomerase G-quadruplex telomerase |
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