Role of CXCL12 and CXCR4 in normal cerebellar development and medulloblastoma

被引:25
作者
Murobushi Ozawa, Patricia Midori [1 ]
Ariza, Carolina Batista [1 ]
Ishibashi, Cintya Mayumi [1 ]
Fujita, Thiago Cezar [1 ]
Banin-Hirata, Bruna Karina [1 ]
Maeda Oda, Julie Massayo [2 ]
Ehara Watanabe, Maria Angelica [1 ]
机构
[1] Univ Estadual Londrina, Ctr Biol Sci, Dept Pathol Sci, Lab Study & Applicat DNA Polymorphisms, Londrina, PR, Brazil
[2] Univ Fed Mato Grosso do Sul, Tres Lagoas, Brazil
关键词
chemokines; cerebellum; CXCL12; CXCR4; childhood cancer; CHEMOKINE RECEPTOR CXCR4; CELL-DERIVED FACTOR-1; PRECURSOR CELLS; BREAST-CANCER; HUMAN BRAIN; STEM-CELLS; C-MYC; EXPRESSION; MIGRATION; SYSTEM;
D O I
10.1002/ijc.29333
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemokines and its receptors have significant impact on physiological and pathological processes and studies concerning their association with tumor biology are subject of great interest in scientific community. CXCL12/CXCR4 axis has been widely studied due to its significant role in tumor microenvironment, but it is also important to development and maintenance of tissues and organs, for example, in the brain and cerebellum. Studies have demonstrated that CXCL12 and CXCR4 are required for normal cerebellar development and that dysfunction in this pathway may be involved with medulloblastoma pathogenesis. In this context, a new molecular subgroup has been suggested based on the importance of the association between CXCR4 overexpression and sonic hedgehog subgroup. Treatment using CXCR4 antagonists showed significant results, evidencing the important role and possible therapeutic capacity of CXCR4 in MB. This review summarizes studies on MB cell biology, focusing on a chemokine-receptor axis, CXCL12/CXCR4, that may have implications for treatment strategies once it can improve life expectancy and reduce neurocognitive sequelae of patients with this neoplasia.
引用
收藏
页码:10 / 13
页数:4
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