Characterization of Hormone-Dependent Pathways in Six Human Prostate-Cancer Cell Lines: A Gene-Expression Study.
Andras FrankoLucia BertiAlke GuirguisJörg HennenlotterRobert WagnerMarcus O ScharpfMartin Hrabĕ de AngelisKatharina WißmillerHeiko LickertArnulf StenzlAndreas L BirkenfeldAndreas PeterHans-Ulrich HäringStefan Z LutzMartin HeniPublished in: Genes (2020)
Prostate cancer (PCa), the most incident cancer in men, is tightly regulated by endocrine signals. A number of different PCa cell lines are commonly used for in vitro experiments, but these are of diverse origin, and have very different cell-proliferation rates and hormone-response capacities. By analyzing the gene-expression pattern of main hormone pathways, we systematically compared six PCa cell lines and parental primary cells. We compared these cell lines (i) with each other and (ii) with PCa tissue samples from 11 patients. We found major differences in the gene-expression levels of androgen, insulin, estrogen, and oxysterol signaling between PCa tissue and cell lines, and between different cell lines. Our systematic characterization gives researchers a solid basis to choose the appropriate PCa cell model for the hormone pathway of interest.
Keyphrases
- gene expression
- prostate cancer
- dna methylation
- cell proliferation
- radical prostatectomy
- type diabetes
- endothelial cells
- end stage renal disease
- cardiovascular disease
- chronic kidney disease
- adipose tissue
- cell cycle
- squamous cell carcinoma
- metabolic syndrome
- stem cells
- papillary thyroid
- bone marrow
- insulin resistance
- peritoneal dialysis
- cell therapy
- young adults
- lymph node metastasis
- pluripotent stem cells
- childhood cancer