Immunohistochemical detection of cancer stem cell related markers CD44 and CD133 in metastatic colorectal cancer patients
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24864242
PubMed Central
PMC4016925
DOI
10.1155/2014/432139
Knihovny.cz E-zdroje
- MeSH
- antigen AC133 MeSH
- antigeny CD44 metabolismus MeSH
- CD antigeny metabolismus MeSH
- glykoproteiny metabolismus MeSH
- imunohistochemie MeSH
- Kaplanův-Meierův odhad MeSH
- kolorektální nádory metabolismus patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádorové biomarkery metabolismus MeSH
- nádorové kmenové buňky metabolismus patologie MeSH
- nádory jater sekundární MeSH
- peptidy metabolismus MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigen AC133 MeSH
- antigeny CD44 MeSH
- CD antigeny MeSH
- CD44 protein, human MeSH Prohlížeč
- glykoproteiny MeSH
- nádorové biomarkery MeSH
- peptidy MeSH
- PROM1 protein, human MeSH Prohlížeč
AIM: The goal of this study was to semiquantitatively detect presence of cancer stem cells markers CD44 and CD133 in immunohistochemically stained paired samples of colorectal cancer (CRC) and colorectal liver metastases (CLM). Level of staining intensity was compared to clinical and pathological characteristics of tumors with the aim to identify impact of CD44 or CD133 expression on tumor behavior. PATIENTS AND METHODS: Formalin fixed paraffin embedded samples from 94 patients with colorectal tumor and liver metastases were collected at Sikl's Department of Pathology. Samples were stained by antibodies against CD44 and CD133. Presence and intensity of staining was assessed semiquantitatively by three trained researchers. RESULTS: Patients with higher level of CD133 staining in CRC had longer disease free interval (Cox-Mantel P = 0.0244), whereas we found no relation between CD44 expression and overall survival or disease free interval. CD133 expression in CRC and CLM differed based on CRC grading; in case of CD44 we found differences in staining intensity in individual stages of tumor lymph node invasion. CONCLUSION: Effect of cancer stem cell markers on prognosis of colorectal cancer can vary depending on pathological classification of tumor, and we have shown that CD133, generally considered to be a negative marker, can bear also clinically positive prognostic information in group of patients with colorectal liver metastases.
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