» Articles » PMID: 11995816

Proteases and the Biology of Glioma Invasion

Overview
Journal J Neurooncol
Publisher Springer
Date 2002 May 9
PMID 11995816
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Despite optimal clinical treatment, the prognosis for malignant gliomas remains poor. One of the primary reasons for treatment failure is not diffuse dissemination, but local invasion. Recently, there has been an increase in information regarding specific molecules that determine the aggressiveness and invasion potential of high-grade astrocytic tumors. In particular, expression of matrix metalloproteases in high-grade gliomas appears to correlate with tissue invasiveness. It is the purpose of the present review to describe the connection between alterations in growth-related genes, protease activity, and tumor biology, and how these connections may suggest potential novel therapeutic targets.

Citing Articles

Cuproptosis key gene FDX1 is a prognostic biomarker and associated with immune infiltration in glioma.

Lu H, Zhou L, Zhang B, Xie Y, Yang H, Wang Z Front Med (Lausanne). 2022; 9:939776.

PMID: 36523779 PMC: 9745336. DOI: 10.3389/fmed.2022.939776.


Semaphorin 3A mediated brain tumor stem cell proliferation and invasion in EGFRviii mutant gliomas.

Higgins D, Caliva M, Schroeder M, Carlson B, Upadhyayula P, Milligan B BMC Cancer. 2020; 20(1):1213.

PMID: 33302912 PMC: 7727139. DOI: 10.1186/s12885-020-07694-4.


Loss of SPINT2 expression frequently occurs in glioma, leading to increased growth and invasion via MMP2.

Pereira M, Celeiro S, Costa A, Pinto F, Popov S, de Almeida G Cell Oncol (Dordr). 2019; 43(1):107-121.

PMID: 31701492 DOI: 10.1007/s13402-019-00475-7.


Author Correction: Genetically engineered cerebral organoids model brain tumor formation.

Bian S, Repic M, Guo Z, Kavirayani A, Burkard T, Bagley J Nat Methods. 2018; 15(9):748.

PMID: 30135560 PMC: 6345371. DOI: 10.1038/s41592-018-0118-8.


Genetically engineered cerebral organoids model brain tumor formation.

Bian S, Repic M, Guo Z, Kavirayani A, Burkard T, Bagley J Nat Methods. 2018; 15(8):631-639.

PMID: 30038414 PMC: 6071863. DOI: 10.1038/s41592-018-0070-7.


References
1.
Liang B, Thornton Jr A, Sandler H, GREENBERG H . Malignant astrocytomas: focal tumor recurrence after focal external beam radiation therapy. J Neurosurg. 1991; 75(4):559-63. DOI: 10.3171/jns.1991.75.4.0559. View

2.
Couldwell W, Antel J, Yong V . Protein kinase C activity correlates with the growth rate of malignant gliomas: Part II. Effects of glioma mitogens and modulators of protein kinase C. Neurosurgery. 1992; 31(4):717-24; discussion 724. DOI: 10.1227/00006123-199210000-00015. View

3.
Baltuch G, Dooley N, Villemure J, Yong V . Protein kinase C and growth regulation of malignant gliomas. Can J Neurol Sci. 1995; 22(4):264-71. DOI: 10.1017/s0317167100039457. View

4.
Yamada T, Yoshiyama Y, Sato H, Seiki M, Shinagawa A, Takahashi M . White matter microglia produce membrane-type matrix metalloprotease, an activator of gelatinase A, in human brain tissues. Acta Neuropathol. 1995; 90(5):421-4. DOI: 10.1007/BF00294800. View

5.
Rao J, Steck P, Mohanam S, Stetler-Stevenson W, Liotta L, Sawaya R . Elevated levels of M(r) 92,000 type IV collagenase in human brain tumors. Cancer Res. 1993; 53(10 Suppl):2208-11. View