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Genome-wide microRNA Expression Profiling in Primary Tumors and Matched Liver Metastasis of Patients with Colorectal Cancer
P. Vychytilova-Faltejskova, M. Pesta, L. Radova, V. Liska, O. Daum, Z. Kala, M. Svoboda, I. Kiss, O. Slaby,
Language English Country Greece
Document type Journal Article
Grant support
NT13549
MZ0
CEP Register
NLK
Free Medical Journals
from 2004 to 2 years ago
PubMed Central
from 2016
Europe PubMed Central
from 2016
PubMed
27365381
Knihovny.cz E-resources
- MeSH
- Genome-Wide Association Study * MeSH
- Adult MeSH
- Colorectal Neoplasms genetics pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- MicroRNAs genetics MeSH
- Liver Neoplasms secondary MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Reproducibility of Results MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Cluster Analysis MeSH
- Gene Expression Profiling * MeSH
- Transcriptome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: Primary tumor spread to the liver is the major cause of disease progression and death in patients with colorectal cancer (CRC). MicroRNAs (miRNAs) are small non-coding RNAs that are involved in cancer development and progression, but their role in metastasis has not been extensively investigated. MATERIALS AND METHODS: Firstly, expression profiling of 752 miRNAs in 20 primary tumors and their corresponding liver metastases was performed. Secondly, validation of the results was carried out on an independent cohort of 66 patients with metastatic CRC using reverse transcription-quantitative polymerase chain (RT-qPCR) reaction. RESULTS: In total, 33 miRNAs were found to be significantly deregulated in liver metastases compared to their primary tumors. Fifteen miRNAs were chosen for subsequent validation, which confirmed significantly reduced expression of miR-143, miR 10b, and miR-28-5p, and increased expression of miR 122, miR-122*, and miR 885-5p in the tissue of liver metastases. CONCLUSION: These results indicate that miRNAs could serve as new therapeutic targets in patients with metastatic CRC.
Central European Institute of Technology Masaryk University Brno Czech Republic
Department of Comprehensive Cancer Care Masaryk Memorial Cancer Institute Brno Czech Republic
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- $a Vychytilová, Petra, $u Central European Institute of Technology, Masaryk University, Brno, Czech Republic Department of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Brno, Czech Republic. $d 1987- $7 xx0165184
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- $a BACKGROUND: Primary tumor spread to the liver is the major cause of disease progression and death in patients with colorectal cancer (CRC). MicroRNAs (miRNAs) are small non-coding RNAs that are involved in cancer development and progression, but their role in metastasis has not been extensively investigated. MATERIALS AND METHODS: Firstly, expression profiling of 752 miRNAs in 20 primary tumors and their corresponding liver metastases was performed. Secondly, validation of the results was carried out on an independent cohort of 66 patients with metastatic CRC using reverse transcription-quantitative polymerase chain (RT-qPCR) reaction. RESULTS: In total, 33 miRNAs were found to be significantly deregulated in liver metastases compared to their primary tumors. Fifteen miRNAs were chosen for subsequent validation, which confirmed significantly reduced expression of miR-143, miR 10b, and miR-28-5p, and increased expression of miR 122, miR-122*, and miR 885-5p in the tissue of liver metastases. CONCLUSION: These results indicate that miRNAs could serve as new therapeutic targets in patients with metastatic CRC.
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- $a Pešta, Martin, $u Department of Biology, Faculty of Medicine in Pilsen, Charles University in Prague, Prague, Czech Republic the Biomedical Center, Faculty of Medicine in Pilsen, Charles University in Prague, Prague, Czech Republic. $d 1976- $7 xx0073915
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