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2',4'-二羟基-6'-甲氧基-3',5'-二甲基查耳酮在人实体癌异种移植模型中的体内抗肿瘤活性。

In vivo antitumor activity by 2',4'-dihydroxy-6'-methoxy-3',5'-dimethylchalcone in a solid human carcinoma xenograft model.

作者信息

Ye Chun-Lin, Liu Jian-Wen, Wei Dong-Zhi, Lu Yan-Hua, Qian Feng

机构信息

State Key Laboratory of Bioreactor Engineering, Institute of Biochemistry, East China University of Science and Technology, Shanghai 200237, People's Republic of China.

出版信息

Cancer Chemother Pharmacol. 2005 Jul;56(1):70-4. doi: 10.1007/s00280-004-0975-y. Epub 2005 Apr 2.

Abstract

Previously we have shown that 2',4'-dihydroxy-6'-methoxy-3',5'-dimethylchalcone (DMC), which is isolated from the buds of Cleistocalyx operculatus, significantly inhibits the growth of human liver cancer SMMC-7721 cells and is able to induce apoptosis of SMMC-7721 cells in vitro. Here we report the antitumor effects of DMC in vivo, using a solid human tumor xenograft mouse model using human liver cancer SMMC-7721 cells. The average tumor weights in the control group and in mice injected with 150 mg/kg DMC were 1.42+/-0.11 g and 0.59+/-0.12 g, respectively. Flow cytometric analysis of the tumor cell population demonstrated an aneuploid peak (representing 33.60+/-0.80% of the total in mice injected with 150 mg/kg DMC). To our knowledge, this is the first time that chalcone compounds have been applied to a human tumor xenograft model.

摘要

此前我们已经表明,从水翁花蕾中分离得到的2',4'-二羟基-6'-甲氧基-3',5'-二甲基查耳酮(DMC)能显著抑制人肝癌SMMC-7721细胞的生长,并在体外诱导SMMC-7721细胞凋亡。在此,我们报告DMC在体内的抗肿瘤作用,采用人肝癌SMMC-7721细胞建立的实体人肿瘤异种移植小鼠模型。对照组和注射150 mg/kg DMC的小鼠的平均肿瘤重量分别为1.42±0.11 g和0.59±0.12 g。对肿瘤细胞群体进行流式细胞术分析显示有一个非整倍体峰(在注射150 mg/kg DMC的小鼠中占总数的33.60±0.80%)。据我们所知,这是首次将查耳酮化合物应用于人类肿瘤异种移植模型。

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