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Endocrine disruption induced by triorganotin (IV) compounds: Impacts in the reproductive and genetic function
Author(s) -
Vicente Sathler Delgado Filho,
Caio Nasser Mancini,
I. V. Silva,
Diego França Pedrosa,
A. Destefani,
Vívian Yochiko Samoto,
Christina Maeda Takiya,
Jones Bernardes Graceli
Publication year - 2010
Publication title -
journal of medical genetics and genomics
Language(s) - English
Resource type - Journals
ISSN - 2141-2278
DOI - 10.5897/jmgg.9000012
Subject(s) - aromatase , tributyltin , nuclear receptor , retinoid x receptor , endocrine system , biology , endocrine disruptor , receptor , peroxisome proliferator activated receptor , endocrinology , medicine , chemistry , gene , hormone , biochemistry , transcription factor , genetics , cancer , ecology , breast cancer
Organotin compounds, such as tributyltin (TBT) and triphenyltin (TPT), are typical environmental contaminants and suspected endocrine-disrupting chemicals because they cause irreversible sexual abnormality (masculinization) in female mollusks, called "imposex". However, it remains unclear whether organotin compounds also cause crucial toxicities in mammalian, including in human and rodents, in their sexual development and reproductive functions. Moreover, these compounds can act as potential competitive inhibitors of aromatase enzyme or others steroidogenic enzymes and recently, it was identified as agonists for retinoid X receptor (RXR) and peroxisome proliferator-activated receptor (PPAR)γ, which are members of the nuclear receptor superfamily. Gene expression of human aromatase is regulated by the activation of PPARγ and/or RXR. In this review, the authors provide a discussion of the cellular, biochemical, and molecular mechanisms by which organotin compounds may cause adverse effects in the modulated genes involved in reproductive function.   Key words: Organotin, endocrine disruptor, aromatase, mammalian reproductive function.

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