Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis.
Sandra M RochaInês SousaInês M GomesPatrícia ArintoPedro Costa-PinheiroEduarda CoutinhoCecília Reis Alves SantosCarmen JerónimoManuel Carlos LemosLuís António Paulino PassarinhaSílvia SocorroCláudio Jorge MaiaPublished in: Life (Basel, Switzerland) (2021)
The Six Transmembrane Epithelial Antigen of the Prostate (STEAP1) is an oncogene overexpressed in several human tumors, particularly in prostate cancer (PCa). However, the mechanisms involved in its overexpression remain unknown. It is well known that epigenetic modifications may result in abnormal gene expression patterns, contributing to tumor initiation and progression. Therefore, this study aimed to analyze the methylation pattern of the STEAP1 gene in PCa versus non-neoplastic cells. Bisulfite amplicon sequencing of the CpG island at the STEAP1 gene promoter showed a higher methylation level in non-neoplastic PNT1A prostate cells than in human PCa samples. Bioinformatic analysis of the GEO datasets also showed the STEAP1 gene promoter as being demethylated in human PCa, and a negative association with STEAP1 mRNA expression was observed. These results are supported by the treatment of non-neoplastic PNT1A cells with DNMT and HDAC inhibitors, which induced a significant increase in STEAP1 mRNA expression. In addition, the involvement of HDAC in the regulation of STEAP1 mRNA expression was corroborated by a negative association between STEAP1 mRNA expression and HDAC4,5,7 and 9 in human PCa. In conclusion, our work indicates that STEAP1 overexpression in PCa can be driven by the hypomethylation of STEAP1 gene promoter.
Keyphrases
- dna methylation
- gene expression
- prostate cancer
- endothelial cells
- genome wide
- induced apoptosis
- induced pluripotent stem cells
- transcription factor
- pluripotent stem cells
- radical prostatectomy
- copy number
- high glucose
- signaling pathway
- genome wide identification
- oxidative stress
- endoplasmic reticulum stress
- molecular docking
- data analysis
- benign prostatic hyperplasia
- pi k akt