Genome-wide microRNA Expression Profiling in Primary Tumors and Matched Liver Metastasis of Patients with Colorectal Cancer
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F16%3A00075969" target="_blank" >RIV/65269705:_____/16:00075969 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14740/16:00088062 RIV/00216208:11140/16:10326732 RIV/00209805:_____/16:N0000097
Result on the web
<a href="https://cgp.iiarjournals.org/content/13/4/311" target="_blank" >https://cgp.iiarjournals.org/content/13/4/311</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Genome-wide microRNA Expression Profiling in Primary Tumors and Matched Liver Metastasis of Patients with Colorectal Cancer
Original language description
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.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30200 - Clinical medicine
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cancer Genomics & Proteomics
ISSN
1109-6535
e-ISSN
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Volume of the periodical
13
Issue of the periodical within the volume
4
Country of publishing house
GR - GREECE
Number of pages
6
Pages from-to
311-316
UT code for WoS article
000379252600007
EID of the result in the Scopus database
2-s2.0-84977156486