(–)-Xanthatin as a Killer of Human Breast Cancer MCF-7 Mammosphere Cells: A Comparative Study with Salinomycin
Experimental evidence accumulated by our research group and others strongly suggests that (–)-xanthatin, a xanthanolide sesquiterpene lactone, exhibits anti-proliferative effects on human breast cancer cells (in vitro) as well as anti-tumor effects in experimental animals (in vivo). In cancer biolog...
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Published in: | Current issues in molecular biology Vol. 44; no. 9; pp. 3849 - 3858 |
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Abstract | Experimental evidence accumulated by our research group and others strongly suggests that (–)-xanthatin, a xanthanolide sesquiterpene lactone, exhibits anti-proliferative effects on human breast cancer cells (in vitro) as well as anti-tumor effects in experimental animals (in vivo). In cancer biology, it is now critically important for anti-cancer agents to selectively target cancer stem cells (CSCs) in order to overcome cancer therapeutic resistance and recurrence. However, it has not yet been established whether (–)-xanthatin abrogates the formation of breast CSCs. In the present study, we utilized chemically synthesized pure (–)-xanthatin and a culture system to obtain mammospheres from human breast cancer MCF-7 cells, which are a CSC-enriched population. We herein demonstrated for the first time that (–)-xanthatin exhibited the ability to kill mammospheres, similar to salinomycin, an established selective killer of CSCs. A possible anti-proliferative mechanism toward mammospheres by (–)-xanthatin is discussed. |
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AbstractList | Experimental evidence accumulated by our research group and others strongly suggests that (–)-xanthatin, a xanthanolide sesquiterpene lactone, exhibits anti-proliferative effects on human breast cancer cells (in vitro) as well as anti-tumor effects in experimental animals (in vivo). In cancer biology, it is now critically important for anti-cancer agents to selectively target cancer stem cells (CSCs) in order to overcome cancer therapeutic resistance and recurrence. However, it has not yet been established whether (–)-xanthatin abrogates the formation of breast CSCs. In the present study, we utilized chemically synthesized pure (–)-xanthatin and a culture system to obtain mammospheres from human breast cancer MCF-7 cells, which are a CSC-enriched population. We herein demonstrated for the first time that (–)-xanthatin exhibited the ability to kill mammospheres, similar to salinomycin, an established selective killer of CSCs. A possible anti-proliferative mechanism toward mammospheres by (–)-xanthatin is discussed. |
Author | Shindo, Mitsuru Hirao-Suzuki, Masayo Takeda, Shuso Aramaki, Hironori |
AuthorAffiliation | 3 Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-koen, Kasuga 816-8580, Japan 4 Department of Molecular Biology, Daiichi University of Pharmacy, 22-1 Tamagawa-cho, Fukuoka 815-8511, Japan 1 Laboratory of Molecular Life Sciences, Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Sanzou 1, Hiroshima 729-0292, Japan 2 Laboratory of Xenobiotic Metabolism and Environmental Toxicology, Faculty of Pharmaceutical Sciences, Hiroshima International University, 5-1-1 Hiro-koshingai, Hiroshima 737-0112, Japan |
AuthorAffiliation_xml | – name: 1 Laboratory of Molecular Life Sciences, Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Sanzou 1, Hiroshima 729-0292, Japan – name: 2 Laboratory of Xenobiotic Metabolism and Environmental Toxicology, Faculty of Pharmaceutical Sciences, Hiroshima International University, 5-1-1 Hiro-koshingai, Hiroshima 737-0112, Japan – name: 3 Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-koen, Kasuga 816-8580, Japan – name: 4 Department of Molecular Biology, Daiichi University of Pharmacy, 22-1 Tamagawa-cho, Fukuoka 815-8511, Japan |
Author_xml | – sequence: 1 givenname: Shuso orcidid: 0000-0003-2193-1421 surname: Takeda fullname: Takeda, Shuso – sequence: 2 givenname: Masayo orcidid: 0000-0002-5626-1950 surname: Hirao-Suzuki fullname: Hirao-Suzuki, Masayo – sequence: 3 givenname: Mitsuru orcidid: 0000-0002-0588-8075 surname: Shindo fullname: Shindo, Mitsuru – sequence: 4 givenname: Hironori orcidid: 0000-0003-0499-0868 surname: Aramaki fullname: Aramaki, Hironori |
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Cites_doi | 10.1016/j.phymed.2013.03.006 10.1016/j.cell.2008.03.027 10.1055/s-0031-1298481 10.1182/blood-2004-10-4135 10.1073/pnas.0706728104 10.1055/s-2006-959537 10.1016/j.cell.2009.06.034 10.1016/j.bcp.2016.06.009 10.21873/anticanres.11507 10.1016/j.bbrc.2020.07.043 10.1007/s00018-016-2362-3 10.1186/bcr2111 10.4161/cc.4.1.1363 10.3727/105221611X13176664479241 10.1073/pnas.0402069101 10.1073/pnas.0530291100 10.1021/tx200046s 10.1038/sj.onc.1206755 10.1016/j.tox.2012.12.019 10.1007/978-3-030-94804-7_1 10.1038/ncb2293 10.2131/jts.38.547 10.1016/j.tet.2012.11.077 10.2131/fts.3.115 10.1248/bpb.b13-00757 10.1038/nrc3920 10.1016/j.tet.2010.08.061 10.2131/fts.2.233 10.1158/0008-5472.CAN-10-0732 10.1139/Y07-104 10.1371/journal.pone.0077281 10.1038/s41420-021-00667-x 10.1111/j.1476-5381.2010.01089.x 10.4103/0973-8258.69154 10.3390/molecules24020359 |
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Title | (–)-Xanthatin as a Killer of Human Breast Cancer MCF-7 Mammosphere Cells: A Comparative Study with Salinomycin |
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