Evidence of the ability of endocrine disrupting compounds to induce testicular germ cell cancer in humans.

Nicolas, N.; Moison, D.; Jampy, A.; Dechamps, N.; Messiaen, S.; Abdallah, S.; benachi, a.; pozzi-gaudin, s.; Rouiller-Fabre, V.; Livera, G.; Guerquin, M.-J.

doi:10.1101/2023.12.22.573063

bioRxiv · 10.1101/2023.12.22.573063

Evidence of the ability of endocrine disrupting compounds to induce testicular germ cell cancer in humans.

Nicolas, N.·Moison, D.·Jampy, A.·Dechamps, N.·Messiaen, S.·Abdallah, S.·benachi, a.·pozzi-gaudin, s.·Rouiller-Fabre, V.·Livera, G.·Guerquin, M.-J.

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Abstract

Testicular cancer is an increasing burden in modern societies and the most common malignancy among young adult males. Environment contaminants, especially endocrine disrupting compounds (EDC), may play a significant role in the development of these cancers through epigenetic alterations occurring during fetal and neonatal development. As long-term studies in humans and suitable experimental models with the potential to develop testicular cancer are lacking, no causal link can be established between endocrine disruptor exposure and testicular cancer incidence. Therefore, we developed an experimental model that recapitulates the differentiation of germ cells from primordial germ cells (pluripotency) into spermatocytes (meiosis) by using xenografted human fetal testis combined with germ cell transplantation into adult testis compartments. Using this model, we demonstrate that long-term fetal exposure (until 12 weeks) to a mixture of Di-2-ethylhexylphthalate (DEHP) and Bisphenol A (BPA), two most prevalent plasticizers, could interfere with fetal germ cell differentiation, leading to carcinogenesis and seminomas. Transcriptome, methylome, and histological analyses reveal that BPA/DEHP exposure induced some significant hallmarks of germ cell tumors to occur: persistent pluripotent and proliferative germ cells, global hypomethylation of CpGs in germ cells, abnormal expression of meiotic markers and fibrotic signatures in fetal testis. Additionally, we found that EDC-exposed fetal germ cells were more likely to develop seminoma in a context that allows spermatogenesis to begin. This study proposes the first experimental evidence that EDC exposure can cause long-term, irreversible lesions in fetal germ cells, which then lead to testicular tumorigenesis in adults.

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Nicolas, N., Moison, D., Jampy, A., Dechamps, N., Messiaen, S., Abdallah, S., benachi, a., pozzi-gaudin, s., Rouiller-Fabre, V., Livera, G., Guerquin, M.-J.. 2023-12-23. Evidence of the ability of endocrine disrupting compounds to induce testicular germ cell cancer in humans.. https://doi.org/10.1101/2023.12.22.573063

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