Novel Pathways for Targeting Tumor Angiogenesis in Metastatic Breast Cancer

被引:32
作者
Harry, Jordan A. [1 ]
Ormiston, Mark L. [1 ,2 ,3 ]
机构
[1] Queens Univ, Dept Med, Kingston, ON, Canada
[2] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON, Canada
[3] Queens Univ, Dept Surg, Kingston, ON, Canada
基金
加拿大健康研究院;
关键词
angiogenesis; breast cancer; vascular endothelial growth factor; bone morphogenetic protein 9; notch signaling; ENDOTHELIAL GROWTH-FACTOR; BONE MORPHOGENETIC PROTEIN; RECEPTOR-LIKE KINASE-1; STEM-CELL CHARACTERISTICS; P38 MAPK INHIBITOR; VESSEL CO-OPTION; VASCULOGENIC MIMICRY; COLORECTAL-CANCER; VASCULAR NORMALIZATION; LY2228820; DIMESYLATE;
D O I
10.3389/fonc.2021.772305
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer is the most common cancer affecting women and is the second leading cause of cancer related death worldwide. Angiogenesis, the process of new blood vessel development from pre-existing vasculature, has been implicated in the growth, progression, and metastasis of cancer. Tumor angiogenesis has been explored as a key therapeutic target for decades, as the blockade of this process holds the potential to reduce the oxygen and nutrient supplies that are required for tumor growth. However, many existing anti-angiogenic approaches, such as those targeting Vascular Endothelial Growth Factor, Notch, and Angiopoietin signaling, have been associated with severe side-effects, limited survival advantage, and enhanced cancer regrowth rates. To address these setbacks, alternative pathways involved in the regulation of tumor angiogenesis are being explored, including those involving Bone Morphogenetic Protein-9 signaling, the Sonic Hedgehog pathway, Cyclooxygenase-2, p38-mitogen-activated protein kinase, and Chemokine Ligand 18. This review article will introduce the concept of tumor angiogenesis in the context of breast cancer, followed by an overview of current anti-angiogenic therapies, associated resistance mechanisms and novel therapeutic targets.
引用
收藏
页数:16
相关论文
共 203 条
[1]   An Autocrine VEGF/VEGFR2 and p38 Signaling Loop Confers Resistance to 4-Hydroxytamoxifen in MCF-7 Breast Cancer Cells [J].
Aesoy, Reidun ;
Sanchez, Betzabe Chavez ;
Norum, Jens Henrik ;
Lewensohn, Rolf ;
Viktorsson, Kristina ;
Linderholm, Barbro .
MOLECULAR CANCER RESEARCH, 2008, 6 (10) :1630-1638
[2]  
Alahmari AK, 2016, AM HEALTH DRUG BENEF, V9, P221
[3]   Phase III Trial Assessing Bevacizumab in Stages II and III Carcinoma of the Colon: Results of NSABP Protocol C-08 [J].
Allegra, Carmen J. ;
Yothers, Greg ;
O'Connell, Michael J. ;
Sharif, Saima ;
Petrelli, Nicholas J. ;
Colangelo, Linda H. ;
Atkins, James N. ;
Seay, Thomas E. ;
Fehrenbacher, Louis ;
Goldberg, Richard M. ;
O'Reilly, Seamus ;
Chu, Luis ;
Azar, Catherine A. ;
Lopa, Samia ;
Wolmark, Norman .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (01) :11-16
[4]   Avastin's commercial march suffers setback [J].
Allison, Malorye .
NATURE BIOTECHNOLOGY, 2010, 28 (09) :879-880
[5]   Incidence and risk of significantly raised blood pressure in cancer patients treated with bevacizumab: an updated meta-analysis [J].
An, Mao Mao ;
Zou, Zui ;
Shen, Hui ;
Liu, Ping ;
Chen, Meng Li ;
Cao, Yong Bing ;
Jiang, Yuan Ying .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2010, 66 (08) :813-821
[6]   Notch signaling: simplicity in design, versatility in function [J].
Andersson, Emma R. ;
Sandberg, Rickard ;
Lendahl, Urban .
DEVELOPMENT, 2011, 138 (17) :3593-3612
[7]  
Arriaga Yull, 2006, Support Cancer Ther, V3, P247, DOI 10.3816/SCT.2006.n.023
[8]   Notch signalling in T-cell lymphoblastic leukaemia/lymphoma and other haematological malignancies [J].
Aster, Jon C. ;
Blacklow, Stephen C. ;
Pear, Warren S. .
JOURNAL OF PATHOLOGY, 2011, 223 (02) :262-273
[9]   Vascular Permeability and Drug Delivery in Cancers [J].
Azzi, Sandy ;
Hebda, Jagoda K. ;
Gavard, Julie .
FRONTIERS IN ONCOLOGY, 2013, 3
[10]   Defective fluid shear stress mechanotransduction mediates hereditary hemorrhagic telangiectasia [J].
Baeyens, Nicolas ;
Larrivee, Bruno ;
Ola, Roxana ;
Hayward-Piatkowskyi, Brielle ;
Dubrac, Alexandre ;
Huang, Billy ;
Ross, Tyler D. ;
Coon, Brian G. ;
Min, Elizabeth ;
Tsarfati, Maya ;
Tong, Haibin ;
Eichmann, Anne ;
Schwartz, Martin A. .
JOURNAL OF CELL BIOLOGY, 2016, 214 (07) :807-816