Sex-dependent regulation of estrogen receptor beta in human colorectal cancer tissue and its relationship with clock genes and VEGF-A expression
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
31928047
DOI
10.33549/physiolres.934352
PII: 934352
Knihovny.cz E-zdroje
- MeSH
- beta receptor estrogenů metabolismus MeSH
- cirkadiánní rytmus - signální peptidy a proteiny metabolismus MeSH
- kohortové studie MeSH
- kolorektální nádory metabolismus MeSH
- lidé MeSH
- pohlavní dimorfismus * MeSH
- senioři MeSH
- vaskulární endoteliální růstový faktor A metabolismus MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- beta receptor estrogenů MeSH
- cirkadiánní rytmus - signální peptidy a proteiny MeSH
- vaskulární endoteliální růstový faktor A MeSH
- VEGFA protein, human MeSH Prohlížeč
The incidence of colorectal cancer (CRC) shows a sex-dependent difference in humans. The aim of this study was to analyze estrogen receptor beta mRNA (ERbeta) expression in patients with CRC with respect to their gender and clinicopathological features. Since cancer progression is accompanied by tumor vascularization, VEGF-A (vascular endothelial growth factor A) transcription was analyzed along with ERbeta mRNA. ERbeta mRNA was also correlated with the expression of clock genes, which are known to influence the cell cycle. ERbeta mRNA expression in females with CRC showed an inverse association with increasing tumor staging that was not observed in males. Lower levels of ERbeta mRNA were observed in females with a higher clinical stage compared with those with earlier-stage tumors. ERbeta mRNA expression showed a significant positive correlation with mRNA of clock genes period 2 and cryptochrome 2 in healthy but not in cancerous tissue in males. Expression of VEGF-A mRNA showed a negative correlation with ERbeta mRNA after splitting of the cohort according to gender and nodus involvement. We propose that gender differences in ERbeta mRNA expression in tumors during the early stages of CRC can partially explain the lower occurrence of CRC in females compared with males.
Citace poskytuje Crossref.org
Downregulation of miR-30c-5p expression in colorectal cancer tissue is sex-dependent