Literature DB >> 31812676

Untangling the association between environmental endocrine disruptive chemicals and the etiology of male genitourinary cancers.

Tiffani J Houston1, Rita Ghosh2.   

Abstract

Endocrine disrupting chemicals disrupt normal physiological function of endogenous hormones, their receptors, and signaling pathways of the endocrine system. Most endocrine disrupting chemicals exhibit estrogen/androgen agonistic and antagonistic activities that impinge upon hormone receptors and related pathways. Humans are exposed to endocrine disrupting chemicals through food, water and air, affecting the synthesis, release, transport, metabolism, binding, function and elimination of naturally occurring hormones. The urogenital organs function as sources of steroid hormones, are targeted end organs, and participate within systemic feedback loops within the endocrine system. The effects of endocrine disruptors can ultimately alter cellular homeostasis leading to a broad range of health effects, including malignancy. Human cancer is characterized by uncontrolled cell proliferation, mechanisms opposing cell-death, development of immortality, induction of angiogenesis, and promotion of invasion/metastasis. While hormonal malignancies of the male genitourinary organs are the second most common types of cancer, the molecular effects of endocrine disrupting chemicals in hormone-driven cancers has yet to be fully explored. In this commentary, we examine the molecular evidence for the involvement of endocrine disrupting chemicals in the genesis and progression of hormone-driven cancers in the prostate, testes, and bladder. We also report on challenges that have to be overcome to drive our understanding of these chemicals and explore the potential avenues of discovery that could ultimately allow the development of tools to prevent cancer in populations where exposure is inevitable.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Environmental endocrine disruptors; Etiology; Male genitourinary cancers; Molecular mechanisms

Mesh:

Substances:

Year:  2019        PMID: 31812676      PMCID: PMC6981057          DOI: 10.1016/j.bcp.2019.113743

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  95 in total

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Authors:  Tomohiko Kanayama; Naoki Kobayashi; Satoru Mamiya; Tsuyoshi Nakanishi; Jun-ichi Nishikawa
Journal:  Mol Pharmacol       Date:  2004-12-20       Impact factor: 4.436

Review 2.  Nongenomic actions of low concentration estrogens and xenoestrogens on multiple tissues.

Authors:  C S Watson; R A Alyea; Y-J Jeng; M Y Kochukov
Journal:  Mol Cell Endocrinol       Date:  2007-05-21       Impact factor: 4.102

Review 3.  Diethylstilboestrol for the treatment of prostate cancer: past, present and future.

Authors:  Rafal Turo; Michal Smolski; Rachel Esler; Magda L Kujawa; Stephen J Bromage; Neil Oakley; Adebanji Adeyoju; Stephen C W Brown; Richard Brough; Andrew Sinclair; Gerald N Collins
Journal:  Scand J Urol       Date:  2013-11-21       Impact factor: 1.612

4.  Evaluation of bisphenol A glucuronidation according to UGT1A1*28 polymorphism by a new LC-MS/MS assay.

Authors:  Tina Trdan Lušin; Robert Roškar; Aleš Mrhar
Journal:  Toxicology       Date:  2011-12-01       Impact factor: 4.221

Review 5.  Are estrogens carcinogenic during development of the testes?

Authors:  J A McLachlan; R R Newbold; S Li; M Negishi
Journal:  APMIS       Date:  1998-01       Impact factor: 3.205

6.  Low doses of the endocrine disruptor bisphenol-A and the native hormone 17beta-estradiol rapidly activate transcription factor CREB.

Authors:  Ivan Quesada; Esther Fuentes; M Carmen Viso-León; Bernat Soria; Cristina Ripoll; Angel Nadal
Journal:  FASEB J       Date:  2002-08-21       Impact factor: 5.191

7.  Persistent DDT metabolite p,p'-DDE is a potent androgen receptor antagonist.

Authors:  W R Kelce; C R Stone; S C Laws; L E Gray; J A Kemppainen; E M Wilson
Journal:  Nature       Date:  1995-06-15       Impact factor: 49.962

8.  Bisphenol A data in NHANES suggest longer than expected half-life, substantial nonfood exposure, or both.

Authors:  Richard W Stahlhut; Wade V Welshons; Shanna H Swan
Journal:  Environ Health Perspect       Date:  2009-01-28       Impact factor: 9.031

9.  Selective retention of hydroxylated PCB metabolites in blood.

Authors:  A Bergman; E Klasson-Wehler; H Kuroki
Journal:  Environ Health Perspect       Date:  1994-05       Impact factor: 9.031

Review 10.  Lesions of testis and epididymis associated with prenatal diethylstilbestrol exposure.

Authors:  B C Bullock; R R Newbold; J A McLachlan
Journal:  Environ Health Perspect       Date:  1988-04       Impact factor: 9.031

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  2 in total

1.  Graphene oxide quantum dots immobilized on mesoporous silica: preparation, characterization and electroanalytical application.

Authors:  Albina Mikhraliieva; Vladimir Zaitsev; Oleg Tkachenko; Michael Nazarkovsky; Yutao Xing; Edilson V Benvenutti
Journal:  RSC Adv       Date:  2020-08-24       Impact factor: 4.036

2.  Endocrine Disruptor Bisphenol A (BPA) Triggers Systemic Para-Inflammation and is Sufficient to Induce Airway Allergic Sensitization in Mice.

Authors:  Lucas Fedele Loffredo; Mackenzie Elyse Coden; Sergejs Berdnikovs
Journal:  Nutrients       Date:  2020-01-28       Impact factor: 5.717

  2 in total

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