Downregulation of miR-30c-5p expression in colorectal cancer tissue is sex-dependent
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
33476170
PubMed Central
PMC8603722
DOI
10.33549/physiolres.934598
PII: 934598
Knihovny.cz E-zdroje
- MeSH
- beta receptor estrogenů genetika metabolismus MeSH
- kohortové studie MeSH
- kolorektální nádory genetika metabolismus patologie MeSH
- lidé MeSH
- mikro RNA biosyntéza genetika MeSH
- míra přežití MeSH
- nádorové biomarkery biosyntéza genetika MeSH
- prognóza MeSH
- senioři MeSH
- sexuální faktory MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- beta receptor estrogenů MeSH
- mikro RNA MeSH
- MIRN30a microRNA, human MeSH Prohlížeč
- nádorové biomarkery MeSH
We report that decreased expression of miR-30c in tumor compared to adjacent tissue is sex-dependent in colorectal cancer (CRC) patients. High expression of miR-30c was associated with better survival in the whole cohort. When the cohort was split into male and female subcohorts, decreased miR-30c expression in tumor compared to adjacent tissue was observed only in males. Expression of miR-30c was decreased in CRC tumor tissue in male patients with nodes involvement compared to those without metastases in nodes and this difference was not observe in females. Next dependency of miR-30c expression on oestrogen receptor beta (ERbeta) mRNA levels in tumor was tested. In males with low expression of ERbeta, we observed a significant decrease in miR-30c levels in patients with nodes involvement compared to those without nodes involvement. This difference was not observed in males with high ERbeta mRNA levels and in females. Accordingly, males with low expression of ERbeta and high expression of miR-30c showed a better survival that those with low expression ERbeta and low expression of miR-30c. It is possible to conclude that whole cohort survival dependence on miR-30c is mostly generated by a subcohort of males with low expression of ERbeta mRNA in tumor tissue.
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