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Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues

The use of bisphenols has become extremely common in our daily lives. Due to the extensive toxic effects of Bisphenol A (BPA), the industry has replaced this endocrine-disrupting chemical (EDC) with its analogues, which have been proven to decrease testosterone levels via several mechanisms, includi...

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Autores principales: Jefferi, Nur Erysha Sabrina, Shamhari, Asma’ ‘Afifah, Hamid, Zariyantey Abd, Budin, Siti Balkis, Zulkifly, Adam Muhammad Zackry, Roslan, Fatin Norisha, Taib, Izatus Shima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219931/
https://www.ncbi.nlm.nih.gov/pubmed/35740303
http://dx.doi.org/10.3390/biomedicines10061281
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author Jefferi, Nur Erysha Sabrina
Shamhari, Asma’ ‘Afifah
Hamid, Zariyantey Abd
Budin, Siti Balkis
Zulkifly, Adam Muhammad Zackry
Roslan, Fatin Norisha
Taib, Izatus Shima
author_facet Jefferi, Nur Erysha Sabrina
Shamhari, Asma’ ‘Afifah
Hamid, Zariyantey Abd
Budin, Siti Balkis
Zulkifly, Adam Muhammad Zackry
Roslan, Fatin Norisha
Taib, Izatus Shima
author_sort Jefferi, Nur Erysha Sabrina
collection PubMed
description The use of bisphenols has become extremely common in our daily lives. Due to the extensive toxic effects of Bisphenol A (BPA), the industry has replaced this endocrine-disrupting chemical (EDC) with its analogues, which have been proven to decrease testosterone levels via several mechanisms, including targeting the steroidogenic acute regulatory (StAR) protein. However, when exposed to BPA and its analogues, the specific mechanism that emerges to target StAR protein regulations remains uncertain. Hence, this review discusses the effects of BPA and its analogues in StAR protein regulation by targeting cAMP-PKA, PLC-PKC, EGFR-MAPK/ERK and Ca(2+)-Nur77. BPA and its analogues mainly lead to decreased LH in blood and increased ERK expression and Ca(2+) influx, with no relationship with the StAR protein regulation in testicular steroidogenesis. Furthermore, the involvement of the cAMP-PKA, PLC-PKC, and Nur77 molecules in StAR regulation in Leydig cells exposed to BPA and its analogues remains questionable. In conclusion, although BPA and its analogues have been found to disrupt the StAR protein, the evidence in connecting the signaling pathways with the StAR regulations in testicular steroidogenesis is still lacking, and more research is needed to draw a solid conclusion.
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spelling pubmed-92199312022-06-24 Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues Jefferi, Nur Erysha Sabrina Shamhari, Asma’ ‘Afifah Hamid, Zariyantey Abd Budin, Siti Balkis Zulkifly, Adam Muhammad Zackry Roslan, Fatin Norisha Taib, Izatus Shima Biomedicines Review The use of bisphenols has become extremely common in our daily lives. Due to the extensive toxic effects of Bisphenol A (BPA), the industry has replaced this endocrine-disrupting chemical (EDC) with its analogues, which have been proven to decrease testosterone levels via several mechanisms, including targeting the steroidogenic acute regulatory (StAR) protein. However, when exposed to BPA and its analogues, the specific mechanism that emerges to target StAR protein regulations remains uncertain. Hence, this review discusses the effects of BPA and its analogues in StAR protein regulation by targeting cAMP-PKA, PLC-PKC, EGFR-MAPK/ERK and Ca(2+)-Nur77. BPA and its analogues mainly lead to decreased LH in blood and increased ERK expression and Ca(2+) influx, with no relationship with the StAR protein regulation in testicular steroidogenesis. Furthermore, the involvement of the cAMP-PKA, PLC-PKC, and Nur77 molecules in StAR regulation in Leydig cells exposed to BPA and its analogues remains questionable. In conclusion, although BPA and its analogues have been found to disrupt the StAR protein, the evidence in connecting the signaling pathways with the StAR regulations in testicular steroidogenesis is still lacking, and more research is needed to draw a solid conclusion. MDPI 2022-05-30 /pmc/articles/PMC9219931/ /pubmed/35740303 http://dx.doi.org/10.3390/biomedicines10061281 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jefferi, Nur Erysha Sabrina
Shamhari, Asma’ ‘Afifah
Hamid, Zariyantey Abd
Budin, Siti Balkis
Zulkifly, Adam Muhammad Zackry
Roslan, Fatin Norisha
Taib, Izatus Shima
Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues
title Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues
title_full Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues
title_fullStr Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues
title_full_unstemmed Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues
title_short Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues
title_sort knowledge gap in understanding the steroidogenic acute regulatory protein regulation in steroidogenesis following exposure to bisphenol a and its analogues
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219931/
https://www.ncbi.nlm.nih.gov/pubmed/35740303
http://dx.doi.org/10.3390/biomedicines10061281
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