首页 | 本学科首页   官方微博 | 高级检索  
     


RHAMM marks proliferative subpopulation of human colorectal cancer stem cells
Authors:Michitaka Nakano  Ryosuke Taguchi  Yoshikane Kikushige  Taichi Isobe  Kohta Miyawaki  Shinichi Mizuno  Nobuhiro Tsuruta  Fumiyasu Hanamura  Kyoko Yamaguchi  Takuji Yamauchi  Hiroshi Ariyama  Hitoshi Kusaba  Masafumi Nakamura  Takahiro Maeda  Calvin J. Kuo  Eishi Baba  Koichi Akashi
Affiliation:1. Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan;2. Department of Health Sciences, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan;3. Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan;4. Division of Precision Medicine, Kyushu University Hospital, Fukuoka, Japan;5. Department of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, California, USA;6. Department of Oncology and Social Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
Abstract:The cancer stem cell (CSC) theory features typically rare self-renewing subpopulations that reconstitute the heterogeneous tumor. Identification of molecules that characterize the features of CSCs is a key imperative for further understanding tumor heterogeneity and for the development of novel therapeutic strategies. However, the use of conventional markers of CSCs is still insufficient for the isolation of bona fide CSCs. We investigated organoids that are miniature forms of tumor tissues by reconstructing cellular diversity to identify specific markers to characterize CSCs in heterogeneous tumors. Here, we report that the receptor for hyaluronan-mediated motility (RHAMM) expresses in a subpopulation of CD44+ conventional human colorectal CSC fraction. Single-cell transcriptomics of organoids highlighted RHAMM-positive proliferative cells that revealed distinct characteristics among the various cell types. Prospectively isolated RHAMM+CD44+ cells from the human colorectal cancer tissues showed highly proliferative characteristics with a self-renewal ability in comparison with the other cancer cells. Furthermore, inhibition of RHAMM strongly suppressed organoid formation in vitro and inhibited tumor growth in vivo. Our findings suggest that RHAMM is a potential therapeutic target because it is a specific marker of the proliferative subpopulation within the conventional CSC fraction.
Keywords:cancer stem cells  colorectal cancer  organoid  CD44  RHAMM
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号