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Identification of CD133+/nestin+ putative cancer stem cells in non-small cell lung cancer
Maria Janikova, Jozef Skarda, Marta Dziechciarkova, Lenka Radova, Jana Chmelova, Veronika Krejci, Eva Sedlakova, Jana Zapletalova, Katerina Langova, Jiri Klein, Ivona Grygarkova, Vitezslav Kolek
Language English Country Czech Republic
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- MeSH
- Antigens, CD MeSH
- Blood Vessels metabolism MeSH
- Epithelium metabolism MeSH
- Financing, Organized 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
- Peptides metabolism MeSH
- Pilot Projects MeSH
- Intermediate Filament Proteins metabolism MeSH
- Nerve Tissue Proteins metabolism MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female 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.
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Lit.: 34
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- $a Janíková, Mária. $7 xx0267892 $u Department of Pathology and Laboratory of Molecular Pathology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic; Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University and University Hospital
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- $a Identification of CD133+/nestin+ putative cancer stem cells in non-small cell lung cancer / $c Maria Janikova, Jozef Skarda, Marta Dziechciarkova, Lenka Radova, Jana Chmelova, Veronika Krejci, Eva Sedlakova, Jana Zapletalova, Katerina Langova, Jiri Klein, Ivona Grygarkova, Vitezslav Kolek
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- $a 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.
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