» Articles » PMID: 23257828

Autocrine Functions of VEGF in Breast Tumor Cells: Adhesion, Survival, Migration and Invasion

Overview
Journal Cell Adh Migr
Specialty Cell Biology
Date 2012 Dec 22
PMID 23257828
Citations 75
Authors
Affiliations
Soon will be listed here.
Abstract

Vascular endothelial growth factor A (VEGF-A) is well known for its key roles in blood vessel growth. Although most studies on VEGF and VEGF receptors have been focused on their functions in angiogenesis and in endothelial cells, the role of VEGF in cancer biology appears as an emerging area of importance. In this context, the presence of VEGF receptors in tumor cells strongly suggests that VEGF-A also promotes a wide range of functions, both in vitro and in vivo, all autocrine functions on tumor cells, including adhesion, survival, migration and invasion. Ultimately, refining our knowledge of VEGF signaling pathways in tumor cells should help us to understand why the current used treatments targeting the VEGF pathway in cancer are not universally effective in inhibiting metastasis tumors, and it should also provide new avenues for future therapies.

Citing Articles

Plasma levels of progranulin, a tumorigenic protein, are persistently elevated during the first month after minimally invasive colorectal cancer resection.

Shantha Kumara H, Hedjar Y, Mitra N, Miyagaki H, Yan X, Cekic V J Gastrointest Oncol. 2024; 15(5):2157-2165.

PMID: 39554587 PMC: 11565126. DOI: 10.21037/jgo-24-114.


Biophysical and Biological Mechanisms of Tumor Treating Fields in Glioblastoma.

Pan J, Eskandar T, Ahmed Z, Agrawal D J Cancer Sci Clin Ther. 2024; 8(3):265-270.

PMID: 39364266 PMC: 11448370. DOI: 10.26502/jcsct.5079249.


The angiogenic role of the alpha 9-nicotinic acetylcholine receptor in triple-negative breast cancers.

Ochirbat S, Kan T, Hsu C, Huang T, Chuang K, Chen M Angiogenesis. 2024; 27(4):827-843.

PMID: 39177676 DOI: 10.1007/s10456-024-09944-6.


FOXK2 amplification promotes breast cancer development and chemoresistance.

Yu Y, Cao W, Cheng F, Shi Z, Han L, Yi J Cancer Lett. 2024; 597:217074.

PMID: 38901667 PMC: 11290987. DOI: 10.1016/j.canlet.2024.217074.


TAD border deletion at the Kit locus causes tissue-specific ectopic activation of a neighboring gene.

Kabirova E, Ryzhkova A, Lukyanchikova V, Khabarova A, Korablev A, Shnaider T Nat Commun. 2024; 15(1):4521.

PMID: 38806452 PMC: 11133455. DOI: 10.1038/s41467-024-48523-7.


References
1.
Wang L, Lau J, Ranjan Patra C, Cao Y, Bhattacharya S, Dutta S . RGS-GAIP-interacting protein controls breast cancer progression. Mol Cancer Res. 2010; 8(12):1591-600. PMC: 3850212. DOI: 10.1158/1541-7786.MCR-10-0209. View

2.
Parker M, Hellman L, Xu P, Fried M, Vander Kooi C . Furin processing of semaphorin 3F determines its anti-angiogenic activity by regulating direct binding and competition for neuropilin. Biochemistry. 2010; 49(19):4068-75. PMC: 2868107. DOI: 10.1021/bi100327r. View

3.
Lee S, Jilani S, Nikolova G, Carpizo D, Iruela-Arispe M . Processing of VEGF-A by matrix metalloproteinases regulates bioavailability and vascular patterning in tumors. J Cell Biol. 2005; 169(4):681-91. PMC: 2171712. DOI: 10.1083/jcb.200409115. View

4.
Rizzolio S, Tamagnone L . Multifaceted role of neuropilins in cancer. Curr Med Chem. 2011; 18(23):3563-75. DOI: 10.2174/092986711796642544. View

5.
Cai H, Reed R . Cloning and characterization of neuropilin-1-interacting protein: a PSD-95/Dlg/ZO-1 domain-containing protein that interacts with the cytoplasmic domain of neuropilin-1. J Neurosci. 1999; 19(15):6519-27. PMC: 6782790. View