Ijiri Masami, Fujiya Mikihiro, Konishi Hiroaki, Tanaka Hiroki, Ueno Nobuhiro, Kashima Shin, Moriichi Kentaro, Sasajima Junpei, Ikuta Katsuya, Okumura Toshikatsu
1 Division of Gastroenterology and Hematology/Oncology, Department of Medicine, Asahikawa Medical University, Asahikawa, Japan.
2 Department of Legal Medicine, Asahikawa Medical University, Asahikawa, Japan.
Tumour Biol. 2017 Jun;39(6):1010428317711311. doi: 10.1177/1010428317711311.
Ferrichrome is known to be a siderophore, but it was recently identified as a tumor-suppressive molecule derived from Lactobacillus casei ATCC334 ( L. casei). In the present study, we investigated the effects of ferrichrome in gastric cancer cells. Cell lines and xenograft models treated with ferrichrome demonstrated growth suppression. The expression levels of cleaved poly (adenosine diphosphate-ribose) polymerase, and cleaved caspase-9 were increased by ferrichrome treatment. Although the tumor-suppressive effects of ferrichrome were almost completely diminished by the iron chelation, the reduction in the intracellular iron by ferrichrome did not correlate with its tumor-suppressive effects. An exhaustive docking simulation indicated that iron-free ferrichrome can make stable conformations with various mammalian molecules, including transporters and receptors. In conclusion, probiotic-derived ferrichrome induced apoptosis in gastric cancer cells. The iron binding site of ferrichrome is the structure responsible for its tumor suppressive function.
高铁色素已知是一种铁载体,但最近它被鉴定为一种源自干酪乳杆菌ATCC334(干酪乳杆菌)的肿瘤抑制分子。在本研究中,我们研究了高铁色素对胃癌细胞的影响。用高铁色素处理的细胞系和异种移植模型显示出生长抑制。高铁色素处理可增加裂解的聚(二磷酸腺苷 - 核糖)聚合酶和裂解的半胱天冬酶 - 9的表达水平。尽管铁螯合几乎完全消除了高铁色素的肿瘤抑制作用,但高铁色素导致的细胞内铁减少与其肿瘤抑制作用无关。详尽的对接模拟表明,无铁的高铁色素可以与包括转运蛋白和受体在内的各种哺乳动物分子形成稳定构象。总之,益生菌衍生的高铁色素可诱导胃癌细胞凋亡。高铁色素的铁结合位点是其肿瘤抑制功能的负责结构。