# Endocrine Disrupting Chemicals and Reproductive Health in Boys and Men

**Authors:** Wiwat Rodprasert, Jorma Toppari, Helena E. Virtanen

PMC · DOI: 10.3389/fendo.2021.706532 · Frontiers in Endocrinology · 2021-10-07

## TL;DR

This paper reviews how exposure to endocrine disrupting chemicals during development may harm male reproductive health, including issues like poor semen quality and testicular cancer.

## Contribution

The paper provides a comprehensive review of how prenatal and early life exposure to EDCs affects male reproductive health outcomes.

## Key findings

- Exposure to antiandrogenic EDCs during fetal development can disrupt testicular development and function.
- Evidence from animal studies supports a link between EDCs and male reproductive disorders.
- Epidemiological studies show mixed results regarding the impact of EDCs on reproductive health.

## Abstract

Male reproductive health has declined as indicated by increasing rates of cryptorchidism, i.e., undescended testis, poor semen quality, low serum testosterone level, and testicular cancer. Exposure to endocrine disrupting chemicals (EDCs) has been proposed to have a role in this finding. In utero exposure to antiandrogenic EDCs, particularly at a sensitive period of fetal testicular development, the so-called ‘masculinization programming window (MPW)’, can disturb testicular development and function. Low androgen effect during the MPW can cause both short- and long-term reproductive disorders. A concurrent exposure to EDCs may also affect testicular function or damage testicular cells. Evidence from animal studies supports the role of endocrine disrupting chemicals in development of male reproductive disorders. However, evidence from epidemiological studies is relatively mixed. In this article, we review the current literature that evaluated relationship between prenatal EDC exposures and anogenital distance, cryptorchidism, and congenital penile abnormality called hypospadias. We review also studies on the association between early life and postnatal EDC exposure and semen quality, hypothalamic-pituitary-gonadal axis hormone levels and testicular cancer.

## Linked entities

- **Diseases:** cryptorchidism (MONDO:0009047), testicular cancer (MONDO:0003510), hypospadias (MONDO:0005345)

## Full-text entities

- **Genes:** ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, Hsd3b5 (hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 5) [NCBI Gene 24470] {aka Hsd1, Hsd3b, RATHSDI}, Cyp17a1 (cytochrome P450, family 17, subfamily a, polypeptide 1) [NCBI Gene 25146] {aka Cyp17}, HSD3B1 (hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1) [NCBI Gene 3283] {aka 3BETAHSD, HSD3B, HSDB3, HSDB3A, SDR11E1}, AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}, Cyp11a1 (cytochrome P450, family 11, subfamily a, polypeptide 1) [NCBI Gene 29680] {aka Cyp11a, Cypxia1, P450(scc), P450scc}, ESR2 (estrogen receptor 2) [NCBI Gene 2100] {aka ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2}, Star (steroidogenic acute regulatory protein) [NCBI Gene 25557], AHR (aryl hydrocarbon receptor) [NCBI Gene 196] {aka FVH3, RP85, bHLHe76}, BCHE (butyrylcholinesterase) [NCBI Gene 590] {aka BCHED, CHE1, CHE2, E1}, ACHE (acetylcholinesterase (Yt blood group)) [NCBI Gene 43] {aka ACEE, ARACHE, N-ACHE, YT}, Gnrh1 (gonadotropin releasing hormone 1) [NCBI Gene 25194] {aka Gnrh, Gnrha, Lhrh, Rgnrhg1, SH-4}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, Insl3 (insulin-like 3) [NCBI Gene 16336] {aka Rlf, Rlnl}, HSD17B13 (hydroxysteroid 17-beta dehydrogenase 13) [NCBI Gene 345275] {aka FLDP, HMFN0376, NIIL497, SCDR9, SDR16C3}, INSL3 (insulin like 3) [NCBI Gene 3640] {aka RLF, RLNL, ley-I-L}, SHBG (sex hormone binding globulin) [NCBI Gene 6462] {aka ABP, SBP, TEBG}
- **Diseases:** male (MESH:D005832), health problems (MESH:D000076082), DDE (MESH:D055959), obese (MESH:D009765), congenital urogenital anomalies (MESH:D014564), factor subfertility (MESH:D007246), Female factor subfertility (MESH:D007247), Hypospadias (MESH:D007021), congenital malformations (OMIM:163000), congenital penile abnormality (MESH:D000013), TGCT (MESH:C563236), genital malformations (MESH:D000091662), malaria (MESH:D008288), IVF (MESH:C537182), Congenital cryptorchidism (MESH:D003456), EDCs (MESH:D004700), male infertility (MESH:D007248), estrogenic (MESH:D056828), Testicular Cancer (MESH:D013736), seminoma (MESH:D018239), varicocele (MESH:D014646), reproductive disorders (MESH:D060737), birth defects (MESH:D000014), cancer (MESH:D009369), TDS (MESH:C537048), germ cell defects (MESH:D009373), AGD (MESH:C567475),  (MESH:D006059)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

305 references — full list in the complete paper: https://tomesphere.com/paper/PMC8530230/full.md

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Source: https://tomesphere.com/paper/PMC8530230