MicroRNA expression profile associated with response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer patients
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
23167930
PubMed Central
PMC3527265
DOI
10.1186/1748-717x-7-195
PII: 1748-717X-7-195
Knihovny.cz E-zdroje
- MeSH
- adenokarcinom genetika metabolismus patologie chirurgie terapie MeSH
- capecitabinum MeSH
- chemoradioterapie * MeSH
- chemorezistence genetika MeSH
- deoxycytidin analogy a deriváty farmakologie terapeutické užití MeSH
- dospělí MeSH
- fluoruracil analogy a deriváty farmakologie terapeutické užití MeSH
- kombinovaná terapie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mikro RNA biosyntéza genetika MeSH
- nádorové proteiny antagonisté a inhibitory fyziologie MeSH
- nádory rekta genetika metabolismus patologie chirurgie terapie MeSH
- neoadjuvantní terapie * MeSH
- pilotní projekty MeSH
- protinádorové antimetabolity farmakologie terapeutické užití MeSH
- regulace genové exprese u nádorů * MeSH
- retrospektivní studie MeSH
- RNA nádorová biosyntéza genetika MeSH
- senioři MeSH
- stanovení celkové genové exprese MeSH
- thymidylátsynthasa antagonisté a inhibitory fyziologie MeSH
- tolerance záření genetika MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- capecitabinum MeSH
- deoxycytidin MeSH
- fluoruracil MeSH
- mikro RNA MeSH
- nádorové proteiny MeSH
- protinádorové antimetabolity MeSH
- RNA nádorová MeSH
- thymidylátsynthasa MeSH
BACKGROUND: Rectal cancer accounts for approximately one third of all colorectal cancers (CRC), which belong among leading causes of cancer deaths worldwide. Standard treatment for locally advanced rectal cancer (cT3/4 and/or cN+) includes neoadjuvant chemoradiotherapy with fluoropyrimidines (capecitabine or 5-fluorouracil) followed by radical surgical resection. Unfortunately, a significant proportion of tumors do not respond enough to the neoadjuvant treatment and these patients are at risk of relapse. MicroRNAs (miRNAs) are small non-coding RNAs playing significant roles in the pathogenesis of many cancers including rectal cancer. MiRNAs could present the new predictive biomarkers for rectal cancer patients. METHODS: We selected 20 patients who underwent neoadjuvant chemoradiotherapy for advanced rectal cancer and whose tumors were classified as most sensitive or resistant to the treatment. These two groups were compared using large-scale miRNA expression profiling. RESULTS: Expression levels of 8 miRNAs significantly differed between two groups. MiR-215, miR-190b and miR-29b-2* have been overexpressed in non-responders, and let-7e, miR-196b, miR-450a, miR-450b-5p and miR-99a* have shown higher expression levels in responders. Using these miRNAs 9 of 10 responders and 9 of 10 non-responders (p < 0.05) have been correctly classified. CONCLUSIONS: Our pilot study suggests that miRNAs are part of the mechanisms that are involved in response of rectal cancer to the chemoradiotherapy and that miRNAs may be promising predictive biomarkers for such patients. In most miRNAs we identified (miR-215, miR-99a*, miR-196b, miR-450b-5p and let-7e), the connection between their expression and radioresistance or chemoresistance to inhibitors of thymidylate synthetase was already established.
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