» Articles » PMID: 26002011

Expression of Metastasis-associated Protein 3 in Human Brain Glioma Related to Tumor Prognosis

Overview
Journal Neurol Sci
Specialty Neurology
Date 2015 May 24
PMID 26002011
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Glioma represents a disparate group of tumors characterized by high invasion ability, and therefore it is of clinical significance to identify molecular markers and therapeutic targets for better clinical management. Previously, metastasis-associated protein family (MTA) is considered to promote tumor cell invasion and metastasis of human malignancies. Recently, the newly identified MTA3 has been shown to play conflicting roles in human malignancies, while the expression pattern and potential clinical significance of MTA3 in human glioma have not been addressed yet. In the present study, we investigated the protein expression of MTA3 by immunohistochemistry assay and analyzed its association with glioma prognosis in 186 cases of patients. Results showed that MTA3 expression was decreased in glioma compared with that in normal brain (P < 0.05). In addition, tumors with high MTA3 expression were more likely to be of low WHO grade (P = 0.005) and reserve of body function (P = 0.014). Survival analysis showed that decreased MTA3 expression was independently associated with unfavorable overall survival of patients (P < 0.001). These results provide the first evidence that MTA3 expression was decreased in human glioma and negatively associated with prognosis of patients, suggesting that MTA3 may play a tumor suppressor role in glioma.

Citing Articles

MTA3 Represses Cancer Stemness by Targeting the SOX2OT/SOX2 Axis.

Du L, Wang L, Gan J, Yao Z, Lin W, Li J iScience. 2019; 22:353-368.

PMID: 31810000 PMC: 6909183. DOI: 10.1016/j.isci.2019.11.009.


MTA3-SOX2 Module Regulates Cancer Stemness and Contributes to Clinical Outcomes of Tongue Carcinoma.

Yao Z, Du L, Xu M, Li K, Guo H, Ye G Front Oncol. 2019; 9:816.

PMID: 31552166 PMC: 6736560. DOI: 10.3389/fonc.2019.00816.


Longitudinal study of leukocyte DNA methylation and biomarkers for cancer risk in older adults.

Bartlett A, Liang J, Sandoval-Sierra J, Fowke J, Simonsick E, Johnson K Biomark Res. 2019; 7:10.

PMID: 31149338 PMC: 6537435. DOI: 10.1186/s40364-019-0161-3.


Novel TG-FGFR1 and TRIM33-NTRK1 transcript fusions in papillary thyroid carcinoma.

Pfeifer A, Rusinek D, Zebracka-Gala J, Czarniecka A, Chmielik E, Zembala-Nozynska E Genes Chromosomes Cancer. 2019; 58(8):558-566.

PMID: 30664823 PMC: 6594006. DOI: 10.1002/gcc.22737.


Risk assessment model constructed by differentially expressed lncRNAs for the prognosis of glioma.

Hu C, Zhou Y, Liu C, Kang Y Oncol Rep. 2018; 40(5):2467-2476.

PMID: 30106138 PMC: 6151882. DOI: 10.3892/or.2018.6639.


References
1.
Noll K, Sullaway C, Ziu M, Weinberg J, Wefel J . Relationships between tumor grade and neurocognitive functioning in patients with glioma of the left temporal lobe prior to surgical resection. Neuro Oncol. 2014; 17(4):580-7. PMC: 4483071. DOI: 10.1093/neuonc/nou233. View

2.
Blaes J, Weiler M, Sahm F, Hentschel B, Osswald M, Czabanka M . NDRG1 prognosticates the natural course of disease in WHO grade II glioma. J Neurooncol. 2014; 117(1):25-32. DOI: 10.1007/s11060-013-1357-2. View

3.
Covington K, Fuqua S . Role of MTA2 in human cancer. Cancer Metastasis Rev. 2014; 33(4):921-8. PMC: 4425804. DOI: 10.1007/s10555-014-9518-0. View

4.
Hofer M, Menke A, Genze F, Gierschik P, Giehl K . Expression of MTA1 promotes motility and invasiveness of PANC-1 pancreatic carcinoma cells. Br J Cancer. 2004; 90(2):455-62. PMC: 2409548. DOI: 10.1038/sj.bjc.6601535. View

5.
Bruning A, Juckstock J, Blankenstein T, Makovitzky J, Kunze S, Mylonas I . The metastasis-associated gene MTA3 is downregulated in advanced endometrioid adenocarcinomas. Histol Histopathol. 2010; 25(11):1447-56. DOI: 10.14670/HH-25.1447. View