“…Dillard et al demonstrated that LNCaP cells express the steroidogenic enzymes necessary for de novo steroidogenesis and indeed synthesized androgens from cholesterol. In contrast, Fankhauser et al more recently demonstrated that in cultures of fresh human BPH and CRPC tissue with T precursors, conversion from DHEA and A‐dione into T was detectable and that the conversion rates were up‐regulated in CRPC, while conversion from cholesterol and Prog into T was undetectable. Our results demonstrate a limited role of intratumoral de novo steroidogenesis in 2 PC cell lines with wild‐type AR, while Preg and Prog did stimulate AR‐regulated cell growth in 1 PC cell line with mutated AR.…”
Our data indicate that at physiological levels of T precursors PC cells can generally convert adrenal androgens, while de novo steroidogenesis is not generally possible in PC cells and is not able to support AR transactivation and PC growth.
“…Dillard et al demonstrated that LNCaP cells express the steroidogenic enzymes necessary for de novo steroidogenesis and indeed synthesized androgens from cholesterol. In contrast, Fankhauser et al more recently demonstrated that in cultures of fresh human BPH and CRPC tissue with T precursors, conversion from DHEA and A‐dione into T was detectable and that the conversion rates were up‐regulated in CRPC, while conversion from cholesterol and Prog into T was undetectable. Our results demonstrate a limited role of intratumoral de novo steroidogenesis in 2 PC cell lines with wild‐type AR, while Preg and Prog did stimulate AR‐regulated cell growth in 1 PC cell line with mutated AR.…”
Our data indicate that at physiological levels of T precursors PC cells can generally convert adrenal androgens, while de novo steroidogenesis is not generally possible in PC cells and is not able to support AR transactivation and PC growth.
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