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
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan
Department of Pathology and Experimental Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558, Japan.
Cancers (Basel). 2019 Feb 3;11(2):177. doi: 10.3390/cancers11020177.
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 , , , , and , 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.
铁过载会引发癌症,并且被认为与包括干性在内的肿瘤发生和癌症进展有关,但具体细节仍不清楚。在此,我们假设癌症中的干性与铁代谢有关,并且调节癌症干细胞(CSCs)中的铁代谢可能是一种新的治疗方法。在本研究中,我们使用了表达特定干细胞基因如 、 、 、 、 和 的小鼠诱导多能干细胞,以及两种具有相似干细胞基因表达的人类癌细胞系。地拉罗司,一种口服可用的铁螯合剂,在体外抑制了干性标志物的表达以及高干性状态细胞的成球作用。与单独使用地拉罗司或顺铂相比,联合治疗具有显著的抗肿瘤效果。铁代谢对于维持癌症干细胞的干性似乎很重要。铁螯合剂与化疗联合可能是一种通过抑制干性进行癌症干细胞靶向治疗的新方法。