» Articles » PMID: 16824034

Molecular Pathways Triggering Glioma Cell Invasion

Overview
Specialty Molecular Biology
Date 2006 Jul 11
PMID 16824034
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

The efficacy of treating malignant gliomas with adjuvant therapies remains largely unsuccessful due to the inability to effectively target invading cells. Although our understanding of glioma oncogenesis has steadily improved, the molecular mechanisms that mediate glioma invasion are still poorly understood. It is clear that genetic alterations in malignant gliomas affect cell proliferation and cell cycle control, which are the targets of most chemotherapeutic agents. However, effective therapy against cell invasion has been less successful. Future treatment protocols must incorporate pharmacotherapeutic strategies that target resistant infiltrative glioma cells as well as proliferating ones. Thus, delineating the point of convergence of signaling pathways, which mediate glioma invasion, proliferation and apoptosis, may identify novel targets that can serve as possible points of therapeutic intervention. The optimization of novel strategies will require reliable preclinical testing using an in vivo animal model of brain invasion. Current applications of existing animal models are not currently optimized or characterized for use in glioma invasion research. As such, the development of a bona fide brain invasion model in vivo must be established. Progress in understanding molecular mechanisms driving glioma invasion will be critical to the success of managing and improving the outcome of patients with this grave disease.

Citing Articles

Glutathione S-Transferase M3 Is Associated with Glycolysis in Intrinsic Temozolomide-Resistant Glioblastoma Multiforme Cells.

Cheng S, Chen N, Wen Z, Yao Z, Tsui K, Kuo H Int J Mol Sci. 2021; 22(13).

PMID: 34209254 PMC: 8268701. DOI: 10.3390/ijms22137080.


Hyaluronic acid induces ROCK-dependent amoeboid migration in glioblastoma cells.

Cui Y, Cole S, Pepper J, Otero J, Winter J Biomater Sci. 2020; 8(17):4821-4831.

PMID: 32749402 PMC: 7473492. DOI: 10.1039/d0bm00505c.


Paradoxical Role of High Mobility Group Box 1 in Glioma: A Suppressor or a Promoter?.

Seidu R, Wu M, Su Z, Xu H Oncol Rev. 2017; 11(1):325.

PMID: 28382190 PMC: 5364998. DOI: 10.4081/oncol.2017.325.


A role for activated Cdc42 in glioblastoma multiforme invasion.

Okura H, Golbourn B, Shahzad U, Agnihotri S, Sabha N, Krieger J Oncotarget. 2016; 7(35):56958-56975.

PMID: 27486972 PMC: 5302965. DOI: 10.18632/oncotarget.10925.


Pivotal role of high-mobility group box 1 (HMGB1) signaling pathways in glioma development and progression.

Angelopoulou E, Piperi C, Adamopoulos C, Papavassiliou A J Mol Med (Berl). 2016; 94(8):867-74.

PMID: 27262996 DOI: 10.1007/s00109-016-1435-y.