Xenoestrogens and cancer understanding the estrogenic effects in the body.
Xenoestrogens and other toxins that affect estrogen signaling. Estrogen signaling is not just confined to estradiol, estrone, and estriol. I want to take it deeper than the visible surface by stepping outside the estrogen that is produced within the body and look at estrogenic signaling that comes from environmental toxins.
You may know them as xenoestrogens. Xenoestrogens are compounds in our environment that have estrogenic effects in the body. The official definition is “man-made non-steroidal organic chemicals which have been released into the environment from agricultural spraying, industrial processes, urban waste or consumer products” .
Common, well-known xenoestrogens include polycyclic aromatic hydrocarbons (PAH), pesticides, polychlorinated biphenyl (PCB), dichloro diphenyl-trichloroethane (DDT), some drugs (e.g., antiepileptic drugs), fungicides, cotinine, phytoestrogens, mycotoxins, bisphenol A (a plastics additive), phthalates, alkylphenols . Even heavy metals have been labeled as metalloestrogens due to their estrogenic activity . All of these xenoestrogens mimic estrogen effect in estrogen signaling via the binding to estrogen receptors and through non-estrogen receptor pathways.
Dr. Nathan Goodyear Explains The Xenoestrogens and Cancer Link
What does the future hold for environmental toxins such as xenoestrogens? What does the future hold for our children and their children’s exposure? Look to the research. A 2004 Environmental Working Group study in collaboration with outside labs found 287 chemicals in the umbilical cord blood of 10 randomly selected births of which 180 are known carcinogens.
Toxins such as Mercury, Lead, Organochlorine pesticides (OCP), Polychlorinated biphenyls (PCB) and many others were among the identified. This Environmental Work Group study was repeated in 2009 in collaboration with 5 independent labs in the U.S., Canada, and Europe and found 232 chemicals in the umbilical cord blood of babies born from 2007-2009. The toxins identified were similar and included Mercury, methylMercury, Lead, Polychlorinated biphenyls, Phalates, Bisphenol A, and Perchlorates.
BPA – bisphenol A is a Xenoestrogen
The perfect example of a xenoestrogen is bisphenol A (BPA). Bisphenol A is a xenoestrogen commonly found in plastics and is definitely one of the more ubiquitous and well-recognized xenoestrogens. BPA, as a xenoestrogen, is a very weak estrogen receptor stimulator .
Many discount the impact of BPA due to its weak estrogenic activity. That would be a mistake. As weak as BPA is in potency, it is strong in its ubiquitous presence in the environment. Prolonged exposure of a low potency toxin is just as dangerous as a short exposure of a high potency toxin. One could argue that it is perhaps more dangerous due to it’s indolent, gradual accumulation and effect.
What the body does with BPA is worse than the BPA itself. Scientists are discovering that the metabolites of BPA are equally prevalent and maybe even more toxic. One such metabolite, 4-methyl-2,4-bis(4-hydroxyphenyl) pent-1-ene or MBP for short, is found to have 1,000 times the estrogenic activity of BPA alone  which makes up for the weak estrogenic activity of BPA.
Additionally, bisphenol A has been shown to cause a shift of the estrogen receptors from an ER-beta dominance to an ER alpha dominance by increasing the genetic encoding of ER-alpha  . This shift to ER-alpha dominance favors inflammation and growth. All this in the low-level blood concentrations commonly found in humans. Most alarming, these low levels are found in our children and are changing our children’s response to hormones (estrogen receptors) even before they are even born .
25 Darbre PD. Metalloestrogens: an emerging class of inorganic xenoestrogens with potential to add to the oestrogenic burden of the human breast. J. Appl. Toxicol. 2006; 26: 191–197.
26 Fucic A, Gamulin M, Ferencic Z, et al. Environmental exposure to xenoestrogens and oestrogen related cancers: reproductive system, breast, lung, kidney, pancreas, and brain. Environ Health. 2012;11 Suppl 1(Suppl 1):S8. Published 2012 Jun 28. doi:10.1186/1476-069X-11-S1-S8.
28 Okuda, T, Takiguchi M, Yoshihara S. In vivo estrogenic potential of 4-methyl-2,4-bis(4- hydroxyphenyl)pent-1-ene, an active metabolite of bisphenol A, in uterus of ovariectomized rats. Toxicol Lett. 2010;197:7-11.
29 Monje L, Varayoud J, Luque EH, Ramos JG. Neonatal exposure to bisphenol A modifies the abundance of estrogen receptor alpha transcripts with alternative 5-untranslated regions in the femal rat preoptic area. J Endocrinol. July 1st, 2007;194:201-212.
30 Takao T et al. Exposure to the environmental estrogen bisphenol A differentially modulated estrogen receptor-alpha and beta immunoreactivity and mRNA in male mouse testis. Life Sci. Jan 24 2004;72(10):1159-69.
31 Schonfelder G, Flick B, Malsness C, Paul M, Chahoud I. In Utero Exposure to low doses of Bisphenol A lead to Long-term deleterious effects in the Vagina. Neoplasia. March 2002;4(2): 98-102.
Dr. Nathan Goodyear is dedicated to disease prevention, disease resolution, and the Wellness Lifestyle through a solution-based, Integrative Medicine approach founded in science. Dr. Goodyear received his Bachelor of Arts from Louisiana Tech University and his Doctor of Medicine from LSU Health Sciences Center.
He is Board Certified in Obstetrics and Gynecology and served as the Chief Resident in Obstetrics and Gynecology at the University of Tennessee. Dr. Goodyear has practiced Integrative Medicine since 2006. Dr. Goodyear is a Fellow in Functional and Regenerative Medicine and served on the board of the American Functional Medicine Association. Dr. Goodyear is a published author, Man Boob Nation–an Integrative medicine approach to low Testosterone published in 2014, and Total Testosterone Transformation published in 2017