Prostate carcinogenesis: inflammatory storms.
Johann S de BonoChristina GuoBora GurelAngelo M De MarzoKaren S SfanosRam S ManiJesús GilCharles G DrakeAndrea AlimontiPublished in: Nature reviews. Cancer (2020)
Prostate cancer is a major cause of cancer morbidity and mortality. Intra-prostatic inflammation is a risk factor for prostate carcinogenesis, with diet, chemical injury and an altered microbiome being causally implicated. Intra-prostatic inflammatory cell recruitment and expansion can ultimately promote DNA double-strand breaks and androgen receptor activation in prostate epithelial cells. The activation of the senescence-associated secretory phenotype fuels further 'inflammatory storms', with free radicals leading to further DNA damage. This drives the overexpression of DNA repair and tumour suppressor genes, rendering these genes susceptible to mutagenic insults, with carcinogenesis accelerated by germline DNA repair gene defects. We provide updates on recent advances in elucidating prostate carcinogenesis and explore novel therapeutic and prevention strategies harnessing these discoveries.
Keyphrases
- dna repair
- prostate cancer
- dna damage
- benign prostatic hyperplasia
- oxidative stress
- radical prostatectomy
- genome wide
- dna damage response
- genome wide identification
- physical activity
- cell proliferation
- papillary thyroid
- squamous cell carcinoma
- single cell
- bioinformatics analysis
- dna methylation
- copy number
- circulating tumor
- bone marrow
- machine learning
- weight loss
- cell free
- genome wide analysis