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A Novel Combination Cancer Therapy with Iron Chelator Targeting Cancer Stem Cells via Suppressing Stemness

Excess iron causes cancer and is thought to be related to carcinogenesis and cancer progression including stemness, but the details remain unclear. Here, we hypothesized that stemness in cancer is related to iron metabolism and that regulating iron metabolism in cancer stem cells (CSCs) may be a nov...

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Autores principales: Katsura, Yuki, Ohara, Toshiaki, Noma, Kazuhiro, Ninomiya, Takayuki, Kashima, Hajime, Kato, Takuya, Sato, Hiroaki, Komoto, Satoshi, Narusaka, Toru, Tomono, Yasuko, Xing, Boyi, Chen, Yuehua, Tazawa, Hiroshi, Kagawa, Shunsuke, Shirakawa, Yasuhiro, Kasai, Tomonari, Seno, Masaharu, Matsukawa, Akihiro, Fujiwara, Toshiyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406536/
https://www.ncbi.nlm.nih.gov/pubmed/30717462
http://dx.doi.org/10.3390/cancers11020177
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author Katsura, Yuki
Ohara, Toshiaki
Noma, Kazuhiro
Ninomiya, Takayuki
Kashima, Hajime
Kato, Takuya
Sato, Hiroaki
Komoto, Satoshi
Narusaka, Toru
Tomono, Yasuko
Xing, Boyi
Chen, Yuehua
Tazawa, Hiroshi
Kagawa, Shunsuke
Shirakawa, Yasuhiro
Kasai, Tomonari
Seno, Masaharu
Matsukawa, Akihiro
Fujiwara, Toshiyoshi
author_facet Katsura, Yuki
Ohara, Toshiaki
Noma, Kazuhiro
Ninomiya, Takayuki
Kashima, Hajime
Kato, Takuya
Sato, Hiroaki
Komoto, Satoshi
Narusaka, Toru
Tomono, Yasuko
Xing, Boyi
Chen, Yuehua
Tazawa, Hiroshi
Kagawa, Shunsuke
Shirakawa, Yasuhiro
Kasai, Tomonari
Seno, Masaharu
Matsukawa, Akihiro
Fujiwara, Toshiyoshi
author_sort Katsura, Yuki
collection PubMed
description Excess iron causes cancer and is thought to be related to carcinogenesis and cancer progression including stemness, but the details remain unclear. Here, we hypothesized that stemness in cancer is related to iron metabolism and that regulating iron metabolism in cancer stem cells (CSCs) may be a novel therapy. In this study, we used murine induced pluripotent stem cells that expressed specific stem cell genes such as Nanog, Oct3/4, Sox2, Klf4, and c-Myc, and two human cancer cell lines with similar stem cell gene expression. Deferasirox, an orally available iron chelator, suppressed expression of stemness markers and spherogenesis of cells with high stemness status in vitro. Combination therapy had a marked antitumor effect compared with deferasirox or cisplatin alone. Iron metabolism appears important for maintenance of stemness in CSCs. An iron chelator combined with chemotherapy may be a novel approach via suppressing stemness for CSC targeted therapy.
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spelling pubmed-64065362019-03-21 A Novel Combination Cancer Therapy with Iron Chelator Targeting Cancer Stem Cells via Suppressing Stemness Katsura, Yuki Ohara, Toshiaki Noma, Kazuhiro Ninomiya, Takayuki Kashima, Hajime Kato, Takuya Sato, Hiroaki Komoto, Satoshi Narusaka, Toru Tomono, Yasuko Xing, Boyi Chen, Yuehua Tazawa, Hiroshi Kagawa, Shunsuke Shirakawa, Yasuhiro Kasai, Tomonari Seno, Masaharu Matsukawa, Akihiro Fujiwara, Toshiyoshi Cancers (Basel) Article Excess iron causes cancer and is thought to be related to carcinogenesis and cancer progression including stemness, but the details remain unclear. Here, we hypothesized that stemness in cancer is related to iron metabolism and that regulating iron metabolism in cancer stem cells (CSCs) may be a novel therapy. In this study, we used murine induced pluripotent stem cells that expressed specific stem cell genes such as Nanog, Oct3/4, Sox2, Klf4, and c-Myc, and two human cancer cell lines with similar stem cell gene expression. Deferasirox, an orally available iron chelator, suppressed expression of stemness markers and spherogenesis of cells with high stemness status in vitro. Combination therapy had a marked antitumor effect compared with deferasirox or cisplatin alone. Iron metabolism appears important for maintenance of stemness in CSCs. An iron chelator combined with chemotherapy may be a novel approach via suppressing stemness for CSC targeted therapy. MDPI 2019-02-03 /pmc/articles/PMC6406536/ /pubmed/30717462 http://dx.doi.org/10.3390/cancers11020177 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Katsura, Yuki
Ohara, Toshiaki
Noma, Kazuhiro
Ninomiya, Takayuki
Kashima, Hajime
Kato, Takuya
Sato, Hiroaki
Komoto, Satoshi
Narusaka, Toru
Tomono, Yasuko
Xing, Boyi
Chen, Yuehua
Tazawa, Hiroshi
Kagawa, Shunsuke
Shirakawa, Yasuhiro
Kasai, Tomonari
Seno, Masaharu
Matsukawa, Akihiro
Fujiwara, Toshiyoshi
A Novel Combination Cancer Therapy with Iron Chelator Targeting Cancer Stem Cells via Suppressing Stemness
title A Novel Combination Cancer Therapy with Iron Chelator Targeting Cancer Stem Cells via Suppressing Stemness
title_full A Novel Combination Cancer Therapy with Iron Chelator Targeting Cancer Stem Cells via Suppressing Stemness
title_fullStr A Novel Combination Cancer Therapy with Iron Chelator Targeting Cancer Stem Cells via Suppressing Stemness
title_full_unstemmed A Novel Combination Cancer Therapy with Iron Chelator Targeting Cancer Stem Cells via Suppressing Stemness
title_short A Novel Combination Cancer Therapy with Iron Chelator Targeting Cancer Stem Cells via Suppressing Stemness
title_sort novel combination cancer therapy with iron chelator targeting cancer stem cells via suppressing stemness
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406536/
https://www.ncbi.nlm.nih.gov/pubmed/30717462
http://dx.doi.org/10.3390/cancers11020177
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