Literature DB >> 3343982

Cytotoxic and mutagenic effects of emodin on cultured mouse carcinoma FM3A cells.

H Morita1, M Umeda, T Masuda, Y Ueno.   

Abstract

Employing a suspension culture of a mouse mammary carcinoma cell line, FM3A cells, the cytotoxicity and induced mutagenicity of emodin (EM) were examined and compared with those of 2-hydroxy-emodin (2-OH-EM), which was identified as an active form of EM in the Ames/microsomes assay. EM was cytotoxic to FM3A cells in concentrations of 1-10 micrograms/ml, and induced 6-thioguanine-resistant (6TGr) mutation. 2-OH-EM was a little more toxic than EM, but induced little mutation.

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Year:  1988        PMID: 3343982     DOI: 10.1016/0165-1218(88)90107-3

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  3 in total

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Authors:  Birgit Dietz; Judy L Bolton
Journal:  Chem Res Toxicol       Date:  2007-03-16       Impact factor: 3.739

Review 2.  Unconventional therapies for cancer: 1. Essiac. The Task Force on Alternative Therapies of the Canadian Breast Cancer Research Initiative.

Authors:  E Kaegi
Journal:  CMAJ       Date:  1998-04-07       Impact factor: 8.262

3.  Species and gender differences affect the metabolism of emodin via glucuronidation.

Authors:  Wei Liu; Lan Tang; Ling Ye; Zheng Cai; Bijun Xia; Jiajie Zhang; Ming Hu; Zhongqiu Liu
Journal:  AAPS J       Date:  2010-05-14       Impact factor: 4.009

  3 in total

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