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KSHV genotypes A and C are more frequent in Kaposi sarcoma lesions from Brazilian patients with and without HIV infection, respectively
Authors:Ramos da Silva Suzane  Ferraz da Silva Ana Paula  Bacchi Maura Moscardi  Bacchi Carlos Eduardo  Elgui de Oliveira Deilson
Institution:Department of Pathophysiology, Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China.
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 LXA(4) 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 LXA(4), effectively inhibited the proliferation, invasion and angiogenesis of tumor in H22 hepatocarcinoma cell bearing mice. These results showed that LXA(4) could be a possible candidate for liver cancer therapy, and blocking the activation of macrophages would be an effective drug target.
Keywords:BSA  bovine serum albumin  ACM  activated macrophage-conditioned media  CCM  control macrophage-conditioned media  DMSO  dimethyl sulfoxide  ECL  enhanced chemiluminescence  ELISA  enzyme-linked immunosorbent assay  FBS  fetal bovine serum  HepG2  human hepatocarcinoma cell line  U937  human monocyte-derived cell line  THP-1  human acute monocytic leukemia cell line  RAW264  7  mouse macrophage-like cell line  H22  mouse hepatocarcinoma cell line  LPS  lipopolysaccharide  PMA  phorbol myristate acetate  LXs  lipoxins  LOXs  lipoxygenases  LXA4  lipoxin A4  NSAIDs  non-steroidal anti-inflammatory drugs  VEGF  vascular endothelial growth factor  PBS  phosphate-buffered saline  TAM  tumor-associated macrophage  TBS  tris-buffered saline  FPRL1  formyl peptide receptor 1
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