摘要
前列腺素类是炎症与癌症的连接环节。mPGES1,前列腺素通路下游的酶,是比抑制癌症发展的COX-2更好的靶点,因为后者抑制作用与心血管及其并发症相关。尽管发现了许多抑制mPGES1的化合物,但是没有一个能作为药物进入市场,因为一些关于它的特异性和不接受的药代动力学特性的问题。炎症和缺氧环境会诱导mPGES1表达,这个表达途径受大量转录因子调控。以这些转录因子为靶点可能成为药物开发过程中的可选途径。这篇综述讨论了这些转录因子的特性和他们与mPGES1基因启动子和抑制剂相关的能力。强调了已报导抑制剂的构效关系。最后,讨论了未来药物开发与研究方向中的实践挑战。这些抑制主要转录因子新型化合物将成为未来开发mPGES1抑制剂的有希望的候选者。
关键词: 癌症,炎症,抑制剂,前列腺素E合成酶 ,转录因子
Current Drug Targets
Title:Transcriptional Regulation of mPGES1 in Cancer: An Alternative Approach to Drug Discovery?
Volume: 18 Issue: 1
Author(s): Meera Ramanan, Mukesh Doble
Affiliation:
关键词: 癌症,炎症,抑制剂,前列腺素E合成酶 ,转录因子
摘要: Prostaglandins serve as the connecting link between inflammation and cancer. mPGES1, the downstream enzyme in the prostaglandin pathway is considered a better target than COX-2 against the progression of cancer due to the cardiovascular and other complications associated with the inhibition of the latter. Despite the discovery of several compounds that inhibit mPGES1 none could enter the market as drugs because of the problems concerning specificity and unacceptable pharmacokinetic properties. Expression of mPGES1 is inducible in conditions of inflammation and hypoxia and its expression is regulated by a number of transcriptional factors. Targeting these transcription factors could be an alternative approach in the drug discovery process. In this review, the characteristics of the transcription factors, their ability to bind to the promoter of mPGES1 gene and the inhibitors against them have been discussed. The Structure Activity Relationship of the reported inhibitors is highlighted. Finally, practical challenges to further the drug development and future research directions are discussed. These novel compounds that are inhibitors of the major transcription factors are promising candidates for further development as inhibitors of mPGES1.
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Cite this article as:
Meera Ramanan, Mukesh Doble , Transcriptional Regulation of mPGES1 in Cancer: An Alternative Approach to Drug Discovery?, Current Drug Targets 2017; 18 (1) . https://dx.doi.org/10.2174/1389450117666160826093137
DOI https://dx.doi.org/10.2174/1389450117666160826093137 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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