Title of article :
Lipoxin A4 and its analog suppress hepatocellular carcinoma via remodeling tumor microenvironment
Author/Authors :
Hao، نويسنده , , Hua and Liu، نويسنده , , Miao and Wu، نويسنده , , Ping and Cai، نويسنده , , Lei and Tang، نويسنده , , Ke and Yi، نويسنده , , Pan and Li، نويسنده , , Li Yongsheng and Chen Qingyi، نويسنده , , Ying and Ye، نويسنده , , Duyun، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
10
From page :
85
To page :
94
Abstract :
Macrophages play an important role in tumor inflammatory microenvironment, lipoxin (LX), the ‘stop signal’ for inflammation, has been extensively studied preclinically for its anti-inflammatory or inflammatory pro-resolving effect. Here, we showed that LXA4 could promote the apoptosis and inhibit the proliferation, migration and angiogenesis of HepG2 hepatocarcinoma cells stimulated by lipopolysaccharide (LPS) or activated macrophage-conditioned media (ACM). Moreover, BML-111, the analog of LXA4, effectively inhibited the proliferation, invasion and angiogenesis of tumor in H22 hepatocarcinoma cell bearing mice. These results showed that LXA4 could be a possible candidate for liver cancer therapy, and blocking the activation of macrophages would be an effective drug target.
Keywords :
Hepatocarcinoma , Lipoxin , C23 , NF-?B , Nucleostemin
Journal title :
Cancer Letters
Serial Year :
2011
Journal title :
Cancer Letters
Record number :
1820227
Link To Document :
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