CCL21型
CCR10
CCL13型
趋化因子受体
CXCL2型
CCL5
CCR1
趋化因子受体
癌症研究
C-C趋化因子受体7型
CCL7型
CXCL16型
C-C趋化因子受体6型
趋化因子
转移
CXCL5型
CXCL9型
CCL19型
CXCL10型
CXCL11型
生物
免疫学
癌症
炎症
T细胞
免疫系统
白细胞介素2受体
遗传学
作者
Hironobu Yanagië,Tomoyuki Hisa,Minoru Ōno,Masazumi Eriguchi
出处
期刊:PubMed
日期:2010-11-01
卷期号:37 (11): 2052-7
被引量:6
摘要
The relationship has become clear between the expression of chemokine/chemokine receptors on cancer cells and the invasion, metastasis and peritoneal dissemination. Many cancer cells express chemokine receptors which are not expressed on the surface of normal tissues. Recently, it has been reported that overexpression of CXCR4/CXCL12 is related with metastasis to lung, liver, lymph nodes and bone marrow, while the overexpression of CCR7/CCL21 is mainly related with lymph node metastasis. We performed a comparative analysis of differential gene expressions related to chemokines/chemokine receptors, and cytokines in established gastric cancer cell lines by cDNA microarray. Upregulated chemokine genes were CCL21, CCL5, CXCL14, CCL2, CXCL1, CXCL8, CXCL7 and CXCL12, which the downregulated chemokines genes were MIP-1alpha and TECK. The upregulated gene of chemokine receptors was CCR-6. In the cancer microenvironment, cancer cells readily formed edematous and inflammatory conditions, easily metastasizing to other organs with the suppression of dendritic cells. The chemokines/chemokine receptors will hopefully become the new targets for cancer therapies for the regulation of metastasis.
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