Chronic Inflammation and Colorectal Cancer: The Role of Vascular Endothelial Growth Factor

被引:46
作者
Hu, Tao [1 ]
Li, Long Fei [1 ]
Shen, Jing [1 ]
Zhang, Lin [1 ]
Cho, Chi Hin [1 ]
机构
[1] Chinese Univ Hong Kong, Fac Med, Sch Biomed Sci, Hong Kong, Hong Kong, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Chronic inflammation; colorectal cancer; vascular endothelial growth factor; LYMPH-NODE METASTASIS; NF-KAPPA-B; HYPOXIA-INDUCIBLE FACTOR; COLON-CARCINOMA CELLS; DNA METHYLATION; CHEMOKINE RECEPTOR; SIGNAL-TRANSDUCTION; ULCERATIVE-COLITIS; NECROSIS-FACTOR; FACTOR THERAPY;
D O I
10.2174/1381612821666150514104244
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Colorectal cancer (CRC) is the third most frequently diagnosed cancer in males and the second in females worldwide. Accumulating evidence has demonstrated that patients with chronic inflammation in bowels have an increased risk to develop CRC. Various inflammatory cells and mediators produced during chronic inflammation are orchestrated through different molecular signaling pathways and lead to the formation of a micro-environment in favor of tumorigenesis. Vascular endothelial growth factor (VEGF), which can be induced by chronic inflammation, plays a pivotal role in tumor angiogenesis as well as tumor growth and metastasis. Anti-angiogenic therapy targeting VEGF and its signaling pathways represents a promising strategy to inhibit colorectal tumorigenesis. Indeed, anti-angiogenic agents modulating VEGF ligands and their receptors have already exhibited great potential in treating patients with CRC, especially when combined with conventional chemotherapeutic agents. This review discusses the promoting role of chronic inflammation in colorectal tumorigenesis at different stages including tumor initiation, promotion, progression and metastasis, highlighting the contributory role of VEGF in angiogenesis during the development from chronic inflammation to CRC. It also describes the clinical significance of anti-VEGF therapy in the treatment of such disease.
引用
收藏
页码:2960 / 2967
页数:8
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