1-(4-甲氧基苯基)-3-(3-phenoxyphenyl) prop-2-en-1-one:一种通过上调p21基因而具有抗肿瘤活性的二苯查尔酮衍生物

Litty Joseph, Lakshmi Ps
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引用次数: 0

摘要

背景与目的:癌症是一种病因复杂的疾病,其特点是异常细胞不受控制地生长。这是一个世界性的重大健康问题。许多天然和合成查尔酮或其衍生物显示出抗癌活性。本研究的目的是评价新型查尔酮衍生物的抗癌活性,并探讨其可能的作用机制。材料与方法:一系列查尔酮3-(3-phenoxyphenyl)-1-苯丙-2-en-1-one (2a);1-(4-氯苯基)-3-(3-phenoxyphenyl) pro- 2-en-1-one (2b);1-(4-氟苯基)-3-(3-phenoxyphenyl) pro- 2-en-1-one (2c);(1 - (4-Nitro-phenyl) 3) - 3-phenoxy-phenyl prop-2-en-1-one (2 d);体外和体内评价了1-(4-甲氧基苯基)-3-(3-苯氧基)prop-2-en-1-one(2e)的细胞毒活性。在道尔顿腹水淋巴瘤诱导的实体瘤模型上测定了这些化合物的体内抗肿瘤活性。通过流式细胞仪和RT- PCR分析进一步分析了有希望的化合物的作用。结果与结论:1-(4-甲氧基苯基)-3-(3-phenoxyphenyl) prop-2-en-1和1-(4-氯苯基)-3-(3-phenoxyphenyl) prop-2-en-1具有体外细胞毒活性、DNA损伤和抗增殖活性。DLA诱导实体瘤模型显示,1-(4-甲氧基苯基)-3-(3-苯氧基苯基)prop-2-en-1-one显著减小肿瘤体积,提高肿瘤抑制率,逆转血液学参数。流式细胞术分析表明,该化合物由于p21过表达导致细胞周期阻滞在G0/G1期。1-(4-甲氧基苯基)-3-(3-苯氧基苯基)pro- 2-en-1-one可能是一种潜在的癌症治疗药物。
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1-(4-Methoxyphenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one: A Diphenyl Chalcone Derivative with Potent Antitumor Activity Via Up-Regulation of p21 Gene
Background and Aim: Cancer is a disease of complex aetiology and is characterised by uncontrolled growth of abnormal cells. It is a major worldwide health problem. Many natural and synthetic chalcone or their derivatives showed anticancer activities. The aim of the present study is to evaluate the anticancer activity of novel chalcone derivatives and also to establish possible mechanism of action. Materials and Methods: A series of chalcones 3-(3-phenoxyphenyl)-1-phenylprop-2-en-1-one (2a); 1-(4-chlorophenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one (2b); 1-(4-fluorophenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one (2c); 1-(4-Nitro-phenyl)-3-(3-phenoxy-phenyl)prop-2-en-1-one (2d); 1-(4-methoxyphenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one(2e) were evaluated for the cytotoxic activity both in vitro and in vivo. The in vivo antitumor activity of these compounds was estimated on Daltons Ascites Lymphoma induced solid tumor model. The effect of promising compound was further analysed by flow cytometer and RT- PCR analysis. Results and Conclusion: 1-(4-methoxyphenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one and 1-(4- chlorophenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one was showed in vitro cytotoxic activity, DNA damage and antiproliferative activity. DLA induced solid tumor model suggested that 1-(4-methoxyphenyl)-3-(3- phenoxy phenyl) prop-2-en-1-one significantly reduced the tumor volume, increase the percentage tumor inhibition and reverse the haematological parameters. Flow cytometry analysis concluded that the compound induces cell cycle arrest at G0/G1 phase due to the over expression of p21. 1-(4-methoxyphenyl)-3-(3- phenoxy phenyl) prop-2-en-1-one may be a potential agent for cancer treatment.
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