Abstract
Purpose
Environmental endocrine-disrupting chemicals (EDCs) are a mixture of chemical compounds capable to interfere with endocrine axis at different levels and to which population is daily exposed. This paper aims to review the relationship between EDCs and breast, prostate, testicle, ovary, and thyroid cancer, discussing carcinogenic activity of known EDCs, while evaluating the impact on public health.
Methods
A literature review regarding EDCs and cancer was carried out with particular interest on meta-analysis and human studies.
Results
The definition of EDCs has been changed through years, and currently there are no common criteria to test new chemicals to clarify their possible carcinogenic activity. Moreover, it is difficult to assess the full impact of human exposure to EDCs because adverse effects develop latently and manifest at different ages, even if preclinical and clinical evidence suggest that developing fetus and neonates are most vulnerable to endocrine disruption.
Conclusion
EDCs represent a major environmental and health issue that has a role in cancer development. There are currently some EDCs that can be considered as carcinogenic, like dioxin and cadmium for breast and thyroid cancer; arsenic, asbestos, and dioxin for prostate cancer; and organochlorines/organohalogens for testicular cancer. New evidence supports the role of other EDCs as possible carcinogenic and pregnant women should avoid risk area and exposure. The relationship between EDCs and cancer supports the need for effective prevention policies increasing public awareness.
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Data availability
Data sharing not applicable to this article as no datasets were generated or analysed during the current study.
Abbreviations
- ADAM33:
-
Metalloproteinase domain 33
- AhR:
-
Hydrocarbon receptor
- ASR:
-
Age-standardized rate
- BPA:
-
Bisphenol A
- BPAF:
-
Bisphenol-AF
- DEHP:
-
Di(2-ethylhexyl)phthalate
- DES:
-
Diethylstilbestrol
- DTC:
-
Differentiated thyroid carcinoma
- DTT:
-
Dichloro-diphenyl-trichloroethane
- EDCs:
-
Endocrine-disrupting chemicals
- ERs:
-
Estrogen receptors
- ER-α:
-
Estrogen receptor-α
- GPI:
-
Glycosylphosphatidylinositol
- HR:
-
Hazard ratio
- IARC:
-
International Agency for Research on Cancer
- ΣLMWP:
-
Low molecular weight phthalates
- MBzP:
-
Mono-benzyl phthalate
- MEC:
-
Multiethnic cohort
- MiBP:
-
Mono-2-isobutyl phthalate
- MSWI:
-
Municipal solid waste incinerator
- NHANES:
-
National Health and Nutrition Examination Survey
- NPCSs:
-
National Priority Contaminated Sites
- NG:
-
Nodular goiter
- OC:
-
Ovarian cancer
- OR:
-
Odd ratio
- PAHs:
-
Polycyclic aromatic hydrocarbons
- PBDE:
-
Polybrominated diphenyl ethers
- PCa:
-
Prostate cancer
- PCBs:
-
Polychlorinated biphenyls
- POPs:
-
Persistent organic pollutants
- PPAR:
-
Human peroxisome proliferator-activated receptor
- PSCA:
-
Prostate stem cell antigen
- PTC:
-
Papillary thyroid carcinoma
- RR:
-
Relative risk
- SERM:
-
Selective estrogen receptor modulator
- TCDD:
-
Tetrachlorodibenzodioxin
- TGCC:
-
Testicular cancer germ cell
- UNEP:
-
United Nations Environment Programme
- WC:
-
Waist circumference
- WHO:
-
World Health Organization
- 2-OH-NAP:
-
2-Hydroxynaphthalene
References
Gassner FX, Reifenstein EC, Algeo JW, Mattox WE (1958) Effects of hormones on growth, fattening, and meat production potential of livestock. Recent Prog Horm Res 14:183–217
Borgert CJ, Sargent E, v., Casella G, Dietrich DR, McCarty LS, Golden RJ. (2012) The human relevant potency threshold: Reducing uncertainty by human calibration of cumulative risk assessments. Regul Toxicol Pharmacol 62(2):313–328
Newbold RR, McLachlan JA, Bullock BC (1985) Progressive proliferative changes in the oviduct of mice following developmental exposure to diethylstilbestrol. Teratog Carcinog Mutagen 5(6):473–480
McLachlan JA, Bullock BC, Newbold RR (1980) Long-term effects on the female mouse genital tract associated with prenatal exposure to diethylstilbestrol. Cancer Res 40(11):3988–3999
Martin O v., Geueke B, Groh KJ, Chevrier J, Fini JB, Houlihan J, et al. 2018 Protocol for a systematic map of the evidence of migrating and extractable chemicals from food contact articles. 2018 Dec 23 [cited 2022 Jul 18]; Available from: https://doi.org/10.5281/zenodo.2525277#.YtXPRv6UOPE.mendeley
Vandenberg LN, Colborn T, Hayes TB, Heindel JJ, Jacobs DR, Lee DH et al (2012) Hormones and endocrine-disrupting chemicals: low-dose effects and nonmonotonic dose responses. Endocr Rev 33(3):378–455
Diamanti-Kandarakis E, Bourguignon JP, Giudice LC, Hauser R, Prins GS, Soto AM et al (2009) Endocrine-disrupting chemicals: an endocrine society scientific statement. Endocr Rev 30(4):293–342
Jenkins S, Rowell C, Wang J, Lamartiniere CA (2007) Prenatal TCDD exposure predisposes for mammary cancer in rats. Reprod Toxicol 23(3):391–396
Soto AM, Sonnenschein C (2010) Environmental causes of cancer: endocrine disruptors as carcinogens. Nat Rev Endocrinol 6(7):363–370
Buha A, Matovic V, Antonijevic B, Bulat Z, Curcic M, Renieri EA et al (2018) Overview of cadmium thyroid disrupting effects and mechanisms. Int J Mol Sci 19(5):1501
List of Classifications – IARC Monographs on the Identification of Carcinogenic Hazards to Humans [Internet]. [cited 2022 Jul 18]. Available from: https://monographs.iarc.who.int/list-of-classifications
Substances identified as endocrine disruptors at EU level | Endocrine Disruptor List [Internet]. [cited 2022 Jul 18]. Available from: https://edlists.org/the-ed-lists/list-i-substances-identified-as-endocrine-disruptors-by-the-eu
Substances under evaluation for endocrine disruption under an EU legislation | Endocrine Disruptor List [Internet]. [cited 2022 Jul 18]. Available from: https://edlists.org/the-ed-lists/list-ii-substances-under-eu-investigation-endocrine-disruption
Substances considered, by the evaluating National Authority, to have endocrine disrupting properties | Endocrine Disruptor List [Internet]. [cited 2022 Jul 18]. Available from: https://edlists.org/the-ed-lists/list-iii-substances-identified-as-endocrine-disruptors-by-participating-national-authorities
Global assessment on the state of the science of endocrine disruptors [Internet]. [cited 2022 Jul 19]. Available from: https://apps.who.int/iris/handle/10665/67357
Thomas Zoeller R, Brown TR, Doan LL, Gore AC, Skakkebaek NE, Soto AM et al (2012) Endocrine-disrupting chemicals and public health protection: a statement of principles from the endocrine society. Endocrinology 153(9):4097–4110
Endocrine Disruptors: from Scientific Evidence to Human Health Protection [Internet]. [cited 2022 Jul 19]. Available from: https://www.europarl.europa.eu/RegData/etudes/STUD/2019/608866/IPOL_STU(2019)608866_EN.pdf
Di Donato M, Cernera G, Giovannelli P, Galasso G, Bilancio A, Migliaccio A et al (2017) Recent advances on bisphenol-A and endocrine disruptor effects on human prostate cancer. Mol Cell Endocrinol 457:35–42
Patrick SM, Bornman MS, Joubert AM, Pitts N, Naidoo V, de Jager C (2016) Effects of environmental endocrine disruptors, including insecticides used for malaria vector control on reproductive parameters of male rats. Reprod Toxicol 61:19–27
Kilian E, Delport R, Bornman MS, de Jager C (2007) Simultaneous exposure to low concentrations of dichlorodiphenyltrichloroethane, deltamethrin, nonylphenol and phytoestrogens has negative effects on the reproductive parameters in male Spraque-Dawley rats. Andrologia 39(4):128–135
Safe S, Wang F, Porter W, Duan R, McDougal A (1998) Ah receptor agonists as endocrine disruptors: antiestrogenic activity and mechanisms. Toxicol Lett 102:343–347
Burgio E, Piscitelli P, Colao A (2018) Environmental Carcinogenesis and transgenerational transmission of carcinogenic risk: from genetics to epigenetics. Int J Environ Res Public Health 15(8):1791
Choi SM, Lee BM (2004) An alternative mode of action of endocrine-disrupting chemicals and chemoprevention. J Toxicol Environ Health B Crit 7(6):451–463
Siegel RL, Miller KD, Jemal A (2020) 2020 Cancer statistics. CA Cancer J Clin 70(1):7–30
Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A et al (2021) Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 71(3):209–249
Nur U, el Reda D, Hashim D, Weiderpass E (2019) A prospective investigation of oral contraceptive use and breast cancer mortality: findings from the Swedish women’s lifestyle and health cohort. BMC Cancer 19(1):1–9
Wan MLY, Co VA, El-Nezami H (2021) Endocrine disrupting chemicals and breast cancer: a systematic review of epidemiological studies. Crit Rev Food Sci Nutr 62(24):6549–6576
Marinković N, Pašalić D, Ferenčak G, Gršković B, Rukavina AS (2010) Dioxins and human toxicity. Arh Hig Rada Toksikol 61(4):445–453
Hockings JK, Thorne PA, Kemp MQ, Morgan SS, Selmin O, Romagnolo DF (2006) The ligand status of the aromatic hydrocarbon receptor modulates transcriptional activation of BRCA-1 promoter by estrogen. Cancer Res 66(4):2224–2232
Warner M, Eskenazi B, Mocarelli P, Gerthoux PM, Samuels S, Needham L et al (2002) Serum dioxin concentrations and breast cancer risk in the Seveso Women’s Health Study. Environ Health Perspect 110(7):625–628
Warner M, Mocarelli P, Samuels S, Needham L, Brambilla P, Eskenazi B (2011) Dioxin exposure and cancer risk in the seveso women’s health study. Environ Health Perspect 119(12):1700–1705
VoPham T, Bertrand KA, Jones RR, Deziel NC, DuPré NC, James P et al (2020) Dioxin exposure and breast cancer risk in a prospective cohort study. Environ Res 186:109516
Danjou AMN, Coudon T, Praud D, Lévêque E, Faure E, Salizzoni P et al (2019) Long-term airborne dioxin exposure and breast cancer risk in a case-control study nested within the French E3N prospective cohort. Environ Int 124:236–248
Polychlorinated Dibenzo-para-dioxins and Polychlorinated Dibenzofurans - NCBI Bookshelf [Internet]. [cited 2022 Jul 19]. Available from: https://www.ncbi.nlm.nih.gov/books/NBK409980/
Filippini T, Torres D, Lopes C, Carvalho C, Moreira P, Naska A et al (2020) Cadmium exposure and risk of breast cancer: a dose-response meta-analysis of cohort studies. Environ Int 142:105879
Tarhonska K, Lesicka M, Janasik B, Roszak J, Reszka E, Braun M et al (2022) Cadmium and breast cancer - current state and research gaps in the underlying mechanisms. Toxicol Lett 361:29–42
Ali I, Damdimopoulou P, Stenius U, Adamsson A, Mäkelä SI, Åkesson A et al (2012) Cadmium-induced effects on cellular signaling pathways in the liver of transgenic estrogen reporter mice. Toxicological Sci 127(1):66–75
Kluxen FM, Diel P, Höfer N, Becker E, Degen GH (2013) The metallohormone cadmium modulates AhR-associated gene expression in the small intestine of rats similar to ethinyl-estradiol. Arch Toxicol 87(4):633–643
Shan Z, Wei Z, Shaikh ZA (2018) Suppression of ferroportin expression by cadmium stimulates proliferation, EMT, and migration in triple-negative breast cancer cells. Toxicol Appl Pharmacol 1(356):36–43
Wei Z, Shan Z, Shaikh ZA (2018) Epithelial-mesenchymal transition in breast epithelial cells treated with cadmium and the role of Snail. Toxicol Appl Pharmacol 1(344):46–55
Luevano J, Damodaran C (2014) A review of molecular events of cadmium-induced carcinogenesis. J Environ Pathol Toxicol Oncol 33(3):183–194
Benedetti M, Zona A, Beccaloni E, Carere M, Comba P (2017) Incidence of breast, prostate, testicular, and thyroid cancer in italian contaminated sites with presence of substances with endocrine disrupting properties. Int J Environ Res Public Health 14(4):355
Zona A, Iavarone I, Buzzoni C, Conti S, Santoro M, Fazzo L et al (2019) [SENTIERI epidemiological study of residents in national priority contaminated sites fifth report]. Epidemiol Prev 43(2):1–208
Sengupta S, Obiorah I, Maximov PY, Curpan R, Jordan VC (2013) Molecular mechanism of action of bisphenol and bisphenol A mediated by oestrogen receptor alpha in growth and apoptosis of breast cancer cells. Br J Pharmacol 169(1):167–178
Kim JY, Choi HG, Lee HM, Lee GA, Hwang KA, Choi KC (2017) Effects of bisphenol compounds on the growth and epithelial mesenchymal transition of MCF-7 CV human breast cancer cells. J Biomed Res 31(4):358–369
Markey CM, Luque EH, de Toro MM, Sonnenschein C, Soto AM (2001) In utero exposure to bisphenol a alters the development and tissue organization of the mouse mammary gland. Biol Reprod 65(4):1215–1223
Acevedo N, Davis B, Schaeberle CM, Sonnenschein C, Soto AM (2013) Perinatally administered bisphenol a as a potential mammary gland carcinogen in rats. Environ Health Perspect. https://doi.org/10.1289/ehp.1306734
Delclos KB, Camacho L, Lewis SM, Vanlandingham MM, Latendresse JR, Olson GR et al (2014) Toxicity evaluation of bisphenol a administered by gavage to sprague dawley rats from gestation day 6 through postnatal day 90. Toxicol Sci 139(1):174–197
Liu G, Cai W, Liu H, Jiang H, Bi Y, Wang H (2021) The Association of Bisphenol a and phthalates with risk of breast cancer: a meta-analysis. Int J Environ Res Public Health 18(5):1–15
Elstner E, Müller C, Koshizuka K, Williamson EA, Park D, Asou H et al (1998) Ligands for peroxisome proliferator-activated receptorgamma and retinoic acid receptor inhibit growth and induce apoptosis of human breast cancer cells in vitro and in BNX mice. Proc Natl Acad Sci U S A 95(15):8806–8811
Yang PJ, Hou MF, Tsai EM, Liang SS, Chiu CC, Ou-Yang F et al (2018) Breast cancer is associated with methylation and expression of the a disintegrin and metalloproteinase domain 33 (ADAM33) gene affected by endocrine-disrupting chemicals. Oncol Rep 40(5):2766–2777
Wu AH, Franke AA, Wilkens LR, Tseng C, Conroy SM, Li Y et al (2021) Urinary phthalate exposures and risk of breast cancer: the Multiethnic Cohort study. Breast Cancer Res 23(1):1–15
Gandaglia G, Leni R, Bray F, Fleshner N, Freedland SJ, Kibel A et al (2021) Epidemiology and prevention of prostate cancer. Eur Urol Oncol. 4(6):877–892
Yang Y, McDonald AC, Wang X, Pan Y, Wang M (2022) Arsenic exposures and prostate cancer risk: a multilevel meta-analysis. J Trace Elem Med Biol 72:126992
Ahn J, Boroje IJ, Ferdosi H, Kramer ZJ, Lamm SH (2020) Prostate cancer incidence in U.S counties and low levels of arsenic in drinking water. Int J Environ Res Public Health 17(3):960
Cardoso APF, Al-Eryani L, Christopher SJ (2018) Arsenic-Induced Carcinogenesis: the Impact of miRNA Dysregulation. Toxicol Sci 165(2):284–290
Shearer MJJ, Wold EA, Umbaugh CS, Lichti CF, Nilsson CL, Figueiredo ML (2016) Inorganic arsenic-related changes in the stromal tumor microenvironment in a prostate cancer cell-conditioned media model. Environ Health Perspect 124(7):1009–1015
Chen C, Xun P, Nishijo M, Carter S, He K (2016) Cadmium exposure and risk of prostate cancer: a meta-analysis of cohort and case-control studies among the general and occupational populations. Sci Rep 6(1):1–7
Eriksen KT, Halkjær J, Meliker JR, McElroy JA, Sørensen M, Tjønneland A et al (2015) Dietary cadmium intake and risk of prostate cancer: a Danish prospective cohort study. BMC Cancer 15(1):1–7
Vijayakumar V, Abern MR, Jagai JS, Kajdacsy-balla A (2021) Observational study of the association between air cadmium exposure and prostate cancer aggressiveness at diagnosis among a nationwide retrospective cohort of 230,540 patients in the united states. Int J Environ Res Public Health 18(16):8333
Dutheil F, Zaragoza-Civale L, Pereira B, Mermillod M, Julien BS et al (2020) Prostate cancer and asbestos: a systematic review and meta-analysis. Perm J. https://doi.org/10.7812/TPP/19.086
Krstev S, Knutsson A (2022) Occupational risk factors for prostate cancer: a meta-analysis. J Cancer Prev 24(2):91–111
Gandaglia G, Leni R, Bray F, Fleshner N, Freedland SJ, Kibel A et al (2021) Epidemiology and prevention of prostate cancer. Eur Urol Oncol 4(6):877–892
Ali I, Julin B, Glynn A, Högberg J, Berglund M, Johansson JE et al (2016) Exposure to polychlorinated biphenyls and prostate cancer: population-based prospective cohort and experimental studies. Carcinogenesis 37(12):1144–1151
Ruder AM, Hein MJ, Hopf NB, Waters MA (2017) Cancer incidence among capacitor manufacturing workers exposed to polychlorinated biphenyls. Am J Ind Med 60(2):198–207
Moore RW, Fritz WA, Schneider AJ, Lin TM, Branam AM, Safe S et al (2016) 2,3,7,8-Tetrachlorodibenzo-p-dioxin has both pro-carcinogenic and anti-carcinogenic effects on neuroendocrine prostate carcinoma formation in TRAMP mice. Toxicol Appl Pharmacol 305:242–249
Medicine I of. Veterans and Agent Orange: Update 2012. Veterans and Agent Orange: Update 2012. 2013 Dec 4;1–986.
Akhtar FZ, Garabrant DH, Ketchum NS, Michalek JE. Cancer in US Air Force veterans of the Vietnam War. J Occup Environ Med [Internet]. 2004 Feb [cited 2022 Jul 20];46(2):123–36. Available from: https://pubmed.ncbi.nlm.nih.gov/14767215/
Chamie K, DeVere White RW, Lee D, Ok JH, Ellison LM. Agent Orange exposure, Vietnam War veterans, and the risk of prostate cancer. Cancer [Internet]. 2008 Nov 1 [cited 2022 Jul 20];113(9):2464–70. Available from: https://pubmed.ncbi.nlm.nih.gov/18666213/
Ansbaugh N, Shannon J, Mori M, Farris PE, Garzotto M. Agent Orange as a risk factor for high-grade prostate cancer. Cancer [Internet]. 2013 Jul 1 [cited 2022 Jul 20];119(13):2399–404. Available from: https://pubmed.ncbi.nlm.nih.gov/23670242/
Prins GS, Ye SH, Birch L, Zhang X, Cheong A, Lin H, et al. Prostate Cancer Risk and DNA Methylation Signatures in Aging Rats following Developmental BPA Exposure: A Dose-Response Analysis. Environ Health Perspect [Internet]. 2017 Jul 1 [cited 2022 Jul 20];125(7). Available from: https://pubmed.ncbi.nlm.nih.gov/28728135/
Prins GS, Hu WY, Xie L, Shi G bin, Hu DP, Birch L, et al. Evaluation of Bisphenol A (BPA) Exposures on Prostate Stem Cell Homeostasis and Prostate Cancer Risk in the NCTR-Sprague-Dawley Rat: An NIEHS/FDA CLARITY-BPA Consortium Study. Environ Health Perspect [Internet]. 2018 Nov 1 [cited 2022 Jul 20];126(11). Available from: https://pubmed.ncbi.nlm.nih.gov/30387366/
Tarapore P, Ying J, Ouyang B, Burke B, Bracken B, Ho SM. Exposure to bisphenol A correlates with early-onset prostate cancer and promotes centrosome amplification and anchorage-independent growth in vitro. PLoS One [Internet]. 2014 Mar 3 [cited 2022 Jul 20];9(3). Available from: https://pubmed.ncbi.nlm.nih.gov/24594937/
Xia B, Wang Y, Wang X, Wu J, Song Q, Sun Z et al (2018) In utero and lactational exposure of DEHP increases the susceptibility of prostate carcinogenesis in male offspring through PSCA hypomethylation. Toxicol Lett 1(292):78–84
Gu Z, Thomas G, Yamashiro J, Shintaku IP, Dorey F, Raitano A, et al. Prostate stem cell antigen (PSCA) expression increases with high gleason score, advanced stage and bone metastasis in prostate cancer. Oncogene [Internet]. 2000 Mar 2 [cited 2022 Jul 20];19(10):1288–96. Available from: https://pubmed.ncbi.nlm.nih.gov/10713670/
Chuang SC, Chen HC, Sun CW, Chen YA, Wang YH, Chiang CJ et al (2020) Phthalate exposure and prostate cancer in a population-based nested case-control study. Environ Res 1(181):108902
Elix C, Pal S, Jones J. The role of peroxisome proliferator-activated receptor gamma in prostate cancer. Asian J Androl [Internet]. 2018 May 1 [cited 2022 Jul 20];20(3):238–43. Available from: https://pubmed.ncbi.nlm.nih.gov/28597850/
Lapinskas PJ, Brown S, Leesnitzer LM, Blanchard S, Swanson C, Cattley RC, et al. Role of PPARalpha in mediating the effects of phthalates and metabolites in the liver. Toxicology [Internet]. 2005 Feb 1 [cited 2022 Jul 20];207(1):149–63. Available from: https://pubmed.ncbi.nlm.nih.gov/15590130/
Krüger T, Long M, Bonefeld-Jørgensen EC. Plastic components affect the activation of the aryl hydrocarbon and the androgen receptor. Toxicology [Internet]. 2008 Apr 18 [cited 2022 Jul 20];246(2–3):112–23.
Richmond O, Ghotbaddini M, Allen C, Walker A, Zahir S, Powell JB (2014) The aryl hydrocarbon receptor is constitutively active in advanced prostate cancer cells. PLoS ONE 9(4):e95058
Rajpert-De ME (2006) Developmental model for the pathogenesis of testicular carcinoma in situ: genetic and environmental aspects. Hum Reprod Update 12(3):303–323
DuMond JW, Singh KP (2007) Gene expression changes and induction of cell proliferation by chronic exposure to arsenic of mouse testicular Leydig cells. J Toxicol Environ Health A 70(13):1150–1154
Bräuner E, v., Lim YH, Koch T, Uldbjerg CS, Gregersen LS, Pedersen MK, et al (2021) Endocrine disrupting chemicals and risk of testicular cancer: a systematic review and meta-analysis. J Clin Endocrinol Metab 106(12):E4834–E4860
Cheng Z, Zhang X, Bassig B, Hauser R, Holford TR, Zheng E et al (2021) Serum polychlorinated biphenyl (PCB) levels and risk of testicular germ cell tumors: A population-based case-control study in Connecticut and Massachusetts. Environ Pollut 273:116453
Cheng Z, Zhang X, Bassig B, Hauser R, Holford TR, Zheng E et al (2021) Dataset of testicular germ cell tumors (TGCT) risk associated with serum polychlorinated biphenyl (PCB) by age at diagnosis and histologic types. Data Brief 36:107014
Hardell L, van Bavel B, Lindström G, Carlberg M, Eriksson M, Dreifaldt AC et al (2004) Concentrations of polychlorinated biphenyls in blood and the risk for testicular cancer. Int J Androl 27(5):282–290
Gaona-Luviano P, Adriana L, Medina-Gaona, Magaña-Pérez K.2020 Epidemiology of ovarian cancer. Chin Clin Oncol. 9(4).
Davis BJ, McCurdy EA, Miller BD, Lucier GW, Tritscher AM (2000) Ovarian tumors in rats induced by chronic 2,3,7,8-Tetrachlorodibenzo-p-dioxin treatment. Cancer Res 60(19):5414–5419
Donna A, Crosignani P, Robutti F, Betta PG, Bocca R, Mariani N et al (1989) Triazine herbicides and ovarian epithelial neoplasms. Scand J Work Environ Health 15(1):47–53
de Roos AJ, Blair A, Rusiecki JA, Hoppin JA, Svec M, Dosemeci M et al (2005) Cancer incidence among glyphosate-exposed pesticide applicators in the agricultural health study. Environ Health Perspect 113(1):49–54
Xie L, Mo M, Jia HX, Liang F, Yuan J, Zhu J (2016) Association between dietary nitrate and nitrite intake and sitespecific cancer risk: evidence from observational studies. Oncotarget 7(35):56915–56932
Nettore IC, Colao A, Macchia PE (2018) Nutritional and environmental factors in thyroid carcinogenesis. Int J Environ Res Public Health 15(8):1735
Fiore M, Conti GO, Caltabiano R, Buffone A, Zuccarello P, Cormaci L et al (2019) Role of emerging environmental risk factors in thyroid cancer: a brief review. Int J Environ Res Public Health 16(7):1185
van Gerwen M, Gold B, Alsen M, Khan MN, Petrick L, Genden E (2021) High thyroid cancer incidence rate in a community near a landfill: a descriptive epidemiological assessment. Toxics. 9(12):325
Fernández-Navarro P, García-Pérez J, Ramis R, Boldo E, López-Abente G (2012) Proximity to mining industry and cancer mortality. Sci Total Environ 435:66–73
Liu B, Chen Y, Li S, Xu Y, Wang Y (2021) Relationship between urinary metabolites of polycyclic aromatic hydrocarbons and risk of papillary thyroid carcinoma and nodular goiter: a case-control study in non-occupational populations. Environ Pollut 269:116158
Calafat AM, Ye X, Valentin-Blasini L, Li Z, Mortensen ME, Wong LY (2017) Co-exposure to non-persistent organic chemicals among American pre-school aged children: a pilot study. Int J Hyg Environ Health 220(2):55–63
Marotta V, Russo G, Gambardella C, Grasso M, la Sala D, Chiofalo MG et al (2019) Human exposure to bisphenol AF and diethylhexylphthalate increases susceptibility to develop differentiated thyroid cancer in patients with thyroid nodules. Chemosphere 1(218):885–894
Gorini F, Bustaffa E, Coi A, Iervasi G, Bianchi F (2020) Bisphenols as environmental triggers of thyroid dysfunction: clues and evidence. Int J Environ Res Public Health 17(8):2654
Kelly M, Connolly L, Dean M (2020) Public awareness and risk perceptions of endocrine disrupting chemicals: a qualitative study. Int J Environ Res Public Health 17(21):1–16
Trasande L, Zoeller RT, Hass U, Kortenkamp A, Grandjean P, Myers JP et al (2016) Burden of disease and costs of exposure to endocrine disrupting chemicals in the European Union: an updated analysis. Andrology 4(4):565–572
Yilmaz B, Terekeci H, Sandal S, Kelestimur F (2020) Endocrine disrupting chemicals: exposure, effects on human health, mechanism of action, models for testing and strategies for prevention. Rev Endocr Metab Disord 21(1):127–147
Gore AC, Chappell VA, Fenton SE, Flaws JA, Nadal A, Prins GS et al (2015) EDC-2: the endocrine society’s second scientific statement on endocrine-disrupting chemicals. Endocr Rev 36(6):1–150
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Modica, R., Benevento, E. & Colao, A. Endocrine-disrupting chemicals (EDCs) and cancer: new perspectives on an old relationship. J Endocrinol Invest 46, 667–677 (2023). https://doi.org/10.1007/s40618-022-01983-4
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DOI: https://doi.org/10.1007/s40618-022-01983-4