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一种新型苯并恶嗪通过促进细胞凋亡和抑制DNA修复的放射增敏活性。

Radiosensitizing activity of a novel Benzoxazine through the promotion of apoptosis and inhibition of DNA repair.

作者信息

Radhamani Suraj, Bradley Christopher, Meehan-Andrews Terri, Ihmaid Saleh K, Al-Rawi Jasim

机构信息

School of Pharmacy and Applied Science, La Trobe Institute of Molecular Sciences, La Trobe University, P.O. Box 199, Bendigo, VIC, 3552, Australia.

出版信息

Invest New Drugs. 2014 Jun;32(3):424-35. doi: 10.1007/s10637-014-0079-4. Epub 2014 Mar 14.

Abstract

The DNA dependant protein kinase (DNA-PK) enzyme plays a major part in the repair of double stranded breaks induced by radiation and hence in the radio-resistance of tumour cells. Inhibitors of DNA-PK have been tested successfully in the past for their ability to sensitize cancer cells to the effects of radiation. Here we present a novel benzoxazine, 8-methyl-2-(morpholine-4yl)-7-(pyridine-3-methoxy)-4H-1,3-benzoxacine-4-one (LTU27) and analyse its ability to cause sensitization of lung cancer and colon cancer cells to radiation. There was a significant reduction in survival rate, increase in apoptosis and inhibition in autophosphorylation of DNA-PK and AKT1 after treating them concomitantly with both radiation and LTU27. The mechanism of action appears to be through inhibition of DNA-PK leading to delayed DNA repair and promotion of apoptosis.

摘要

DNA依赖性蛋白激酶(DNA-PK)在修复辐射诱导的双链断裂中起主要作用,因此在肿瘤细胞的放射抗性中也起主要作用。过去已经成功测试了DNA-PK抑制剂使癌细胞对辐射作用敏感的能力。在此,我们展示了一种新型苯并恶嗪,8-甲基-2-(吗啉-4-基)-7-(吡啶-3-甲氧基)-4H-1,3-苯并恶嗪-4-酮(LTU27),并分析了其使肺癌和结肠癌细胞对辐射敏感的能力。在用辐射和LTU27同时处理后,细胞存活率显著降低,细胞凋亡增加,DNA-PK和AKT1的自磷酸化受到抑制。其作用机制似乎是通过抑制DNA-PK导致DNA修复延迟并促进细胞凋亡。

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