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p53抑制剂pifithrin-α在体内和体外均能抑制萤火虫荧光素酶的活性。

The p53-inhibitor pifithrin-alpha inhibits firefly luciferase activity in vivo and in vitro.

作者信息

Rocha Sonia, Campbell Kirsteen J, Roche Kevin C, Perkins Neil D

机构信息

School of Life Sciences, Division of Gene Regulation and Expression MSI/WTB, Complex Dow Street University of Dundee Dundee, DD1 5EH, Scotland, United Kingdom.

出版信息

BMC Mol Biol. 2003 Sep 11;4:9. doi: 10.1186/1471-2199-4-9.

Abstract

BACKGROUND

Pifithrin-alpha is a small molecule inhibitor of p53 transcriptional activity. It has been proposed that the use of pifithrin-alpha in conjunction with chemotherapeutic and radiation therapies for cancer will reduce the side effects of these treatments in normal tissue that still contains wild type p53. In addition, pifithrin-alpha provides a useful tool in the laboratory to investigate the function of p53 in model systems.

RESULTS

While investigating the effects of pifithrin-alpha on the transcriptional activity of NF-kappaB, we observed a strong inhibition of reporter plasmids containing the firefly luciferase gene. Firefly luciferase is one of the most commonly used enzymes in reporter gene assays. In contrast, no inhibition of reporter plasmids containing Renilla luciferase or chloramphenicol acetyltransferase was observed. The inhibition of firefly luciferase activity by pifithrin-alpha was observed both in vivo and in vitro. Pifithrin-alpha did not inhibit firefly luciferase protein expression, but rather suppressed light production/emission, since addition of exogenous pifithrin-alpha to active extracts inhibited this activity. Furthermore, pifithrin-alpha also inhibited recombinant firefly luciferase protein activity.

CONCLUSIONS

Among its other biological activities, pifithrin-alpha is an inhibitor of firefly luciferase activity. Caution must therefore be taken when using this compound, which has been characterised as an inhibitor of p53 transcriptional activity, to investigate effects on gene expression using transiently transfected reporter plasmids. Furthermore, these results demonstrate that when using novel compounds, the choice of vectors used in the experimental procedures might be of great importance for the correct conclusions to be made.

摘要

背景

Pifithrin-α是一种p53转录活性的小分子抑制剂。有人提出,将Pifithrin-α与癌症的化疗和放疗联合使用,将减少这些治疗对仍含有野生型p53的正常组织产生的副作用。此外,Pifithrin-α为实验室研究p53在模型系统中的功能提供了一个有用的工具。

结果

在研究Pifithrin-α对NF-κB转录活性的影响时,我们观察到对含有萤火虫荧光素酶基因的报告质粒有强烈抑制作用。萤火虫荧光素酶是报告基因检测中最常用的酶之一。相比之下,未观察到对含有海肾荧光素酶或氯霉素乙酰转移酶的报告质粒有抑制作用。在体内和体外均观察到Pifithrin-α对萤火虫荧光素酶活性的抑制作用。Pifithrin-α不抑制萤火虫荧光素酶蛋白表达,而是抑制光的产生/发射,因为向活性提取物中添加外源性Pifithrin-α会抑制这种活性。此外,Pifithrin-α还抑制重组萤火虫荧光素酶蛋白活性。

结论

在其其他生物学活性中,Pifithrin-α是萤火虫荧光素酶活性的抑制剂。因此,在使用这种已被表征为p53转录活性抑制剂的化合物,通过瞬时转染报告质粒来研究对基因表达的影响时,必须谨慎。此外,这些结果表明,在使用新型化合物时,实验过程中所用载体的选择对于得出正确结论可能非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23e2/212280/3b76574844f1/1471-2199-4-9-1.jpg

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