VEGF and angiopoietin signaling in tumor angiogenesis and metastasis

被引:432
|
作者
Saharinen, Pipsa [1 ,2 ]
Eklund, Lauri [3 ,4 ]
Pulkki, Kristina [1 ,6 ,7 ,8 ]
Bono, Petri [5 ]
Alitalo, Kari [1 ,6 ,7 ,8 ]
机构
[1] Univ Helsinki, Res Programs Unit, Biomedicum Helsinki, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Dept Virol, FIN-00014 Helsinki, Finland
[3] Univ Oulu, Oulu Ctr Cell Matrix Res, Bioctr Oulu, Oulu 90014, Finland
[4] Univ Oulu, Dept Med Biochem & Mol Biol, Oulu 90014, Finland
[5] Univ Helsinki, Cent Hosp, Dept Oncol, FIN-00029 Helsinki, Finland
[6] Univ Helsinki, Dept Pathol, Haartman Inst, FIN-00014 Helsinki, Finland
[7] Univ Helsinki, Inst Mol Med Finland, FIN-00014 Helsinki, Finland
[8] Univ Helsinki, Cent Hosp, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
ENDOTHELIAL-GROWTH-FACTOR; RECEPTOR TYROSINE KINASE; LYMPH-NODE LYMPHANGIOGENESIS; INTERSTITIAL FLUID PRESSURE; RENAL-CELL CARCINOMA; ANTI-VEGF; FACTOR-C; TIE2-EXPRESSING MONOCYTES; VASCULAR NORMALIZATION; VESSEL DEVELOPMENT;
D O I
10.1016/j.molmed.2011.01.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Solid tumors require blood vessels for growth and dissemination, and lymphatic vessels as additional conduits for metastatic spread. The identification of growth factor receptor pathways regulating angiogenesis has led to the clinical approval of the first antiangiogenic molecules targeted against the vascular endothelial growth factor (VEGF)-VEGF receptor (VEGFR)-2 pathway. However, in many cases resistance to anti-VEGF-VEGFR therapy occurs, and thus far the clinical benefit has been limited to only modest improvements in overall survival. Therefore, novel treatment modalities are required. Here, we discuss the) members of the VEGF VEGFR family as well as the angiopoietin growth factors and their Tie receptors as potential novel targets for antiangiogenic and antilymphangiogenic therapies.
引用
收藏
页码:347 / 362
页数:16
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