» Articles » PMID: 18172261

Stem Cell Marker CD133 Affects Clinical Outcome in Glioma Patients

Overview
Journal Clin Cancer Res
Specialty Oncology
Date 2008 Jan 4
PMID 18172261
Citations 274
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: The CD133 antigen has been identified as a putative stem cell marker in normal and malignant brain tissues. In gliomas, it is used to enrich a subpopulation of highly tumorigenic cancer cells. According to the cancer stem cell hypothesis, CD133-positive cells determine long-term tumor growth and, therefore, are suspected to influence clinical outcome. To date, a correlation between CD133 expression in primary tumor tissues and patients' prognosis has not been reported.

Experimental Design: To address this question, we analyzed the expression of the CD133 stem cell antigen in a series of 95 gliomas of various grade and histology by immunohistochemistry on cryostat sections. Staining data were correlated with patient outcome.

Results: By multivariate survival analysis, we found that both the proportion of CD133-positive cells and their topological organization in clusters were significant (P < 0.001) prognostic factors for adverse progression-free survival and overall survival independent of tumor grade, extent of resection, or patient age. Furthermore, proportion of CD133-positive cells was an independent risk factor for tumor regrowth and time to malignant progression in WHO grade 2 and 3 tumors.

Conclusions: These findings constitute the first conclusive evidence that CD133 stem cell antigen expression correlates with patient survival in gliomas, lending support to the current cancer stem cell hypothesis.

Citing Articles

Oncogenic Mutations and the Tumor Microenvironment: Drivers of Non-Small Cell Lung Cancer Progression.

Mitrakas A, Kakouratos C, Lamprou I, Xanthopoulou E, Koukourakis M Cancers (Basel). 2025; 17(5).

PMID: 40075700 PMC: 11899603. DOI: 10.3390/cancers17050853.


Expression features of targets for anti-glioma CAR-T cell immunotherapy.

Zhang P, Li C, Wang Y, Chi X, Sun T, Zhang Q J Neurooncol. 2024; 171(1):179-189.

PMID: 39467936 DOI: 10.1007/s11060-024-04855-4.


Role of Extracellular Vesicles in the Progression of Brain Tumors.

Schiera G, Di Liegro C, Vento F, Di Liegro I Biology (Basel). 2024; 13(8).

PMID: 39194524 PMC: 11351128. DOI: 10.3390/biology13080586.


Glutamine deprivation in glioblastoma stem cells triggers autophagic SIRT3 degradation to epigenetically restrict CD133 expression and stemness.

Xing Z, Jiang X, Chen Y, Wang T, Li X, Wei X Apoptosis. 2024; 29(9-10):1619-1631.

PMID: 39068621 DOI: 10.1007/s10495-024-02003-x.


Molecular diversity in isocitrate dehydrogenase-wild-type glioblastoma.

Fares J, Wan Y, Mair R, Price S Brain Commun. 2024; 6(2):fcae108.

PMID: 38646145 PMC: 11032202. DOI: 10.1093/braincomms/fcae108.