Sex-dependent regulation of estrogen receptor beta in human colorectal cancer tissue and its relationship with clock genes and VEGF-A expression
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
31928047
DOI
10.33549/physiolres.934352
PII: 934352
Knihovny.cz E-resources
- MeSH
- Estrogen Receptor beta metabolism MeSH
- Circadian Rhythm Signaling Peptides and Proteins metabolism MeSH
- Cohort Studies MeSH
- Colorectal Neoplasms metabolism MeSH
- Humans MeSH
- Sex Characteristics * MeSH
- Aged MeSH
- Vascular Endothelial Growth Factor A metabolism MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Estrogen Receptor beta MeSH
- Circadian Rhythm Signaling Peptides and Proteins MeSH
- Vascular Endothelial Growth Factor A MeSH
- VEGFA protein, human MeSH Browser
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.
References provided by Crossref.org
Downregulation of miR-30c-5p expression in colorectal cancer tissue is sex-dependent