论文部分内容阅读
To review the implication of CXCR4 for gastrointestinal cancer, a “Pubmed” analysis was performed in order to evaluate the relevance of CXCR4 and its ligands for gastrointestinal cancers. Search terms applied were “cancer, malignoma, esophageal, gastric, colon, colorectal, hepatic, pancreatic, CXCR4, SDF-1α, and SDF-1b”. CXCR4 expression correlated with dissemination of diverse gastrointestinal malignomas. The CXCR4 ligand SDF-1α might act as “chemorepellent” while SDF-1b might act as “chemorepellent” for CTLs, inducing tumor rejection. The paracrine expression of SDF-1α was furthermore closely associated with neoangiogenesis. CXCR4 and its ligands influence the dissemination, immune rejection, and neoangiogenesis of human gastrointestinal cancers. Inhibition of CXCR4 might be an interesting therapeutic option.
To review the implication of CXCR4 for gastrointestinal cancer, a “Pubmed” analysis was performed in order to evaluate the relevance of CXCR4 and its ligands for gastrointestinal cancers. Search terms applied were “cancer, malignoma, esophageal, gastric, colon, The CXCR4 ligand SDF-1α might act as ”chemorepellent “ while SDF-1b might act as The ”chemorepellent" for CTLs, inducing tumor rejection. The paracrine expression of SDF-1α was very closely associated with neoangiogenesis. CXCR4 and its ligands influence the dissemination, immune rejection, and neoangiogenesis of human gastrointestinal cancers. Inhibition of CXCR4 might be an interesting therapeutic option.