cxcl17 expression by tumor cells recruits cd11b+gr1highf480? cells and promotes tumor progressioncxcl17肿瘤细胞表达的新兵cd11b + gr1highf480 细胞和促进肿瘤的进展.pdfVIP
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cxcl17expressionbytumorcellsrecruitscd11bgr1highf480?cellsandpromotestumorprogressioncxcl17肿瘤细胞表达的新兵cd11bgr1highf480细胞和促进肿瘤的进展
CXCL17 Expression by Tumor Cells Recruits
CD11b+Gr1highF4/802 Cells and Promotes Tumor
Progression
1,2 3 4 4 2
Aya Matsui , Hideaki Yokoo , Yoichi Negishi , Yoko Endo-Takahashi , Nicole A. L. Chun ,
2 5 5 5 6 7
Ichiro Kadouchi , Ryo Suzuki , Kazuo Maruyama , Yukihiko Aramaki , Kentaro Semba , Eiji Kobayashi ,
2 1
Masafumi Takahashi , Takashi Murakami *
1 Laboratory of Tumor Biology, Takasaki University of Health and Welfare, Takasaki, Gunma, Japan, 2 Division of Bioimaging Sciences, Center for Molecular Medicine, Jichi
Medical University, Shimotsuke, Tochigi, Japan, 3 Department of Human Pathology, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan,
4 Department of Drug and Gene Delivery Systems, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan, 5 Department of Biopharmaceutics,
School of Pharmaceutical Sciences, Teikyo University, Sagamihara, Kanagawa, Japan, 6 Department of Life Science and Medical Bio-Science, Waseda University,
Wakamatsu, Shinjuku, Tokyo, Japan, 7 Division of Development for Advanced Medical Technology, Jichi Medical University, Shimotsuke, Tochigi, Japan
Abstract
Background: Chemokines are involved in multiple aspects of pathogenesis and cellular trafficking in tumorigenesis. In this
study, we report that the latest member of the C-X-C-type chemokines, CXCL17 (DMC/VCC-1), recruits immature myeloid-
derived cells and enhances early tumor progression.
Methodology/Principal Findings: CXCL17 was preferentially expressed in some aggre
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