» Articles » PMID: 11595114

Brain Metastases: Biology and the Role of the Brain Microenvironment

Overview
Journal Curr Oncol Rep
Publisher Current Science
Specialty Oncology
Date 2001 Oct 12
PMID 11595114
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Metastatic lesions constitute the most frequently occurring malignancy in the brain, and their detection portends a grim prognosis. Efforts to treat these lesions have failed partly because the biologic processes that govern their development are poorly understood. In recent years, it has become evident that metastases occur as a result of a multistep process involving a rigorous natural selection of cells in the primary tumor that bear molecular and biologic characteristics permitting brain metastasis. In addition, recent studies have uncovered the importance of the brain microenvironment and its contribution to the metastatic process. The development of targeted therapies against brain metastases demands a better understanding of these molecular processes and the factors that influence them. This review examines the interplay between tumor cells and host brain tissue in the context of our current understanding of the role of various molecules involved in the metastatic process.

Citing Articles

Significance of Trask protein interactions in brain metastatic cohorts of lung cancers.

Wu H, Shang L, Chen R, Yang S, Wang S, Wang J Tumour Biol. 2015; 36(6):4181-7.

PMID: 25775948 DOI: 10.1007/s13277-015-3053-7.


Development of a preclinical therapeutic model of human brain metastasis with chemoradiotherapy.

Martinez-Aranda A, Hernandez V, Picon C, Modolell I, Sierra A Int J Mol Sci. 2013; 14(4):8306-27.

PMID: 23591844 PMC: 3645744. DOI: 10.3390/ijms14048306.


Characterisation of Walker 256 breast carcinoma cells from two tumour cell banks as assessed using two models of secondary brain tumours.

Lewis K, Harford-Wright E, Vink R, Ghabriel M Cancer Cell Int. 2013; 13(1):5.

PMID: 23374226 PMC: 3576291. DOI: 10.1186/1475-2867-13-5.


Neurotrophin-3 modulates breast cancer cells and the microenvironment to promote the growth of breast cancer brain metastasis.

Louie E, Chen X, Coomes A, Ji K, Tsirka S, Chen E Oncogene. 2012; 32(35):4064-77.

PMID: 23001042 PMC: 3998718. DOI: 10.1038/onc.2012.417.


Neurosurgical treatment of breast cancer metastases to the neurocranium.

Stark A Patholog Res Int. 2011; 2011:549847.

PMID: 21209717 PMC: 3010687. DOI: 10.4061/2011/549847.


References
1.
Brooks P, Clark R, Cheresh D . Requirement of vascular integrin alpha v beta 3 for angiogenesis. Science. 1994; 264(5158):569-71. DOI: 10.1126/science.7512751. View

2.
Saaristo A, Karpanen T, Alitalo K . Mechanisms of angiogenesis and their use in the inhibition of tumor growth and metastasis. Oncogene. 2001; 19(53):6122-9. DOI: 10.1038/sj.onc.1203969. View

3.
Reyes-Reyes M, Mora N, Zentella A, Rosales C . Phosphatidylinositol 3-kinase mediates integrin-dependent NF-kappaB and MAPK activation through separate signaling pathways. J Cell Sci. 2001; 114(Pt 8):1579-89. DOI: 10.1242/jcs.114.8.1579. View

4.
Diamond M, Springer T . The dynamic regulation of integrin adhesiveness. Curr Biol. 1994; 4(6):506-17. DOI: 10.1016/s0960-9822(00)00111-1. View

5.
Aigner S, Sthoeger Z, Fogel M, Weber E, Zarn J, Ruppert M . CD24, a mucin-type glycoprotein, is a ligand for P-selectin on human tumor cells. Blood. 1997; 89(9):3385-95. View