Identification of CD133+/nestin+ putative cancer stem cells in non-small cell lung cancer
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
21293543
DOI
10.5507/bp.2010.048
Knihovny.cz E-resources
- MeSH
- AC133 Antigen MeSH
- Antigens, CD metabolism MeSH
- Blood Vessels metabolism MeSH
- Epithelium metabolism MeSH
- Glycoproteins metabolism MeSH
- Humans MeSH
- Neoplastic Stem Cells metabolism MeSH
- Lung Neoplasms blood supply metabolism MeSH
- Carcinoma, Non-Small-Cell Lung blood supply metabolism MeSH
- Nestin MeSH
- Peptides metabolism MeSH
- Pilot Projects MeSH
- Intermediate Filament Proteins metabolism MeSH
- Nerve Tissue Proteins metabolism MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- AC133 Antigen MeSH
- Antigens, CD MeSH
- Glycoproteins MeSH
- NES protein, human MeSH Browser
- Nestin MeSH
- Peptides MeSH
- PROM1 protein, human MeSH Browser
- Intermediate Filament Proteins MeSH
- Nerve Tissue Proteins MeSH
AIMS: No effective treatment for lung cancer exists currently. One reason for this, is the development of drug resistance, assumed to be associated with cancer stem cell (CSCs) emergence within the tumour. This pilot study aimed to identify CSCs in 121 non-small cell lung cancer (NSCLC) patient samples via detection of the expression of stem cell markers - CD133 and nestin. MATERIAL AND METHODS: Archived paraffin blocks of 121 patient samples were prepared as Tissue Microarrays (TMA). Indirect immunohistochemical staining was used to determine the level of expression of CD133 and nestin. Double immunofluorescence staining was used to investigate the co-expression of these two markers. To determine the correlation between expression of nestin and CD133 with the length of asymptomatic period and overall patient survival we used the Kaplan-Meyer analysis. RESULTS: CD133 expression was detected in 22 (19%), nestin in the epithelium in 74 (66%) and vasculature in 78 (70%) of patients. Co-expression of these two markers was found in 21 (17%) patients in less than 1% of positive cells without impact on disease free or overall survival. CONCLUSIONS: We identified CD133(+)/nestin(+) cells as novel potential markers of lung cancer CSCs.
References provided by Crossref.org
Nestin as a marker of cancer stem cells