1997
DOI: 10.1016/s0890-6238(96)00203-1
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Leydig cell hyperplasia and adenoma formation: Mechanisms and relevance to humans

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Cited by 117 publications
(78 citation statements)
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“…Dopamine agonists and other chemicals, such as methoxychlor, carbamazepine, and o,p′-DDD, shown to inhibit oocyte maturation in fishes, have been shown to induce Leydig cell hyperplasia and adenomas in mammalian species (reviewed by Clegg et al, 1997).…”
Section: Discussionmentioning
confidence: 99%
“…Dopamine agonists and other chemicals, such as methoxychlor, carbamazepine, and o,p′-DDD, shown to inhibit oocyte maturation in fishes, have been shown to induce Leydig cell hyperplasia and adenomas in mammalian species (reviewed by Clegg et al, 1997).…”
Section: Discussionmentioning
confidence: 99%
“…25,42 There is clear evidence that LH plays a pivotal role in development of the Leydig cell population and stimulating T production in adults. 43,44 In addition, LH is believed to be the main trophic hormone that causes Leydig cell adenomas, 43 while there is evidence showing that estrogens induce Leydig cell adenomas via their ability to increase LH action in certain strains of mice. 45,46 However, our recent study showed that mice with a marked overexpression of hCG do not develop Leydig cell hyperplasia in adulthood.…”
Section: Discussionmentioning
confidence: 99%
“…In rats, PFOA is a peroxisome proliferator activated receptor (PPAR) agonist causing liver toxicity (12,13) with hepatomegaly and hepatic necrosis, and biochemical effects characteristic of PPAR agonists (14). PFOA promotes liver carcinogenesis in rats (15), and causes Leydig-cell testicular tumors and acinar cell pancreatic tumors (16,17), through non-genotoxic mechanisms (18,19) with questionable human relevance. The human half-life of PFOA was between four and five years for retirees with previous heavy occupational exposure (20), much longer than in laboratory animals.…”
Section: Introductionmentioning
confidence: 99%