2019
DOI: 10.1016/j.cbi.2019.02.027
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Endocrine disruptors of inhibiting testicular 3β-hydroxysteroid dehydrogenase

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Cited by 39 publications
(14 citation statements)
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“…In male laboratory animals, phthalates interfere with sex hormone steroidogenesis in reproductive organs via alterations in steroidogenic gene transcription [205]. HSD3B, the steroidogenic enzyme that catalyzes the conversion of 3β-hydroxysteroids into 3-keto-steroids, has been identified as a phthalate target in testicular tissue [206] (Table 6).…”
Section: Non-human Animalsmentioning
confidence: 99%
“…In male laboratory animals, phthalates interfere with sex hormone steroidogenesis in reproductive organs via alterations in steroidogenic gene transcription [205]. HSD3B, the steroidogenic enzyme that catalyzes the conversion of 3β-hydroxysteroids into 3-keto-steroids, has been identified as a phthalate target in testicular tissue [206] (Table 6).…”
Section: Non-human Animalsmentioning
confidence: 99%
“…Ketoconazole is an antifungal agent that is also able to competitively bind to the AR 193 . Ketoconazole has also been shown to inhibit enzymes important for testosterone synthesis 194 and is under investigation in combination with docetaxel (NCT00212095) 195 . In addition, TRC253, a novel competitive inhibitor of AR has been shown to be an antagonist to wildtype AR as well as all tested AR mutants 196 , including AR F877L, a mutation occurring in the LBD of AR 197 .…”
Section: Second Generation Antiandrogensmentioning
confidence: 99%
“…CYP7B1 is present in reproductive organs and is an enzyme that metabolizes androgens ( Stiles et al, 2009 ). HSD3B1 is an important gene that catalyzes the conversion of pregnenolone to progesterone ( Zhang et al, 2019 ). Among the genes upregulated in SF, STC1 can inhibit FSH-induced progesterone production ( Luo et al, 2004 ).…”
Section: Discussionmentioning
confidence: 99%