# Environmental endocrine disruptors and endometrial cancer: a systematic review of epidemiological studies

**Authors:** Dalila Incognito, Claudia Gelsomino, Antonio Picone, Giuseppe Ettore, Carla Ettore, Giosuè Giordano Incognito, Giordana Di Mauro, Mariacarmela Santarpia, M’Hammed Aguennouz, Silvana Parisi, Giuliana Ciappina, Massimiliano Berretta

PMC · DOI: 10.3389/fendo.2026.1719784 · Frontiers in Endocrinology · 2026-02-12

## TL;DR

This review examines how exposure to endocrine-disrupting chemicals may be linked to an increased risk of endometrial cancer, with cadmium showing the strongest association.

## Contribution

The study systematically reviews epidemiological evidence linking endocrine disruptors to endometrial cancer, highlighting cadmium as a key risk factor.

## Key findings

- Cadmium exposure is most frequently associated with endometrial cancer risk, particularly in lean postmenopausal women.
- Bisphenol A and phthalates show inconsistent associations with endometrial cancer.
- Nonylphenol and octylphenol are positively linked to endometrial cancer in one study.

## Abstract

Endometrial cancer (EC) is a hormone-dependent malignancy whose global incidence is steadily rising. Increasing evidence suggests that exposure to endocrine-disrupting chemicals (EDCs) may contribute to EC development through interference with hormonal signaling mediated by estrogen receptors (ER). This systematic review aimed to synthesize the available epidemiological evidence on the association between exposure to EDCs and the risk of EC. A comprehensive search of MEDLINE, EMBASE, Scopus, the Cochrane Library, and ClinicalTrials.gov was conducted up to April 2025, following PRISMA 2020 recommendations. Eligible studies included observational or interventional designs assessing quantified exposure to EDCs and EC incidence or risk. Eight studies met the inclusion criteria (five case-control, two cohort, and one randomized controlled trial), comprising 2, 609 EC cases and 1, 577 controls. Cadmium emerged as the EDC most frequently associated with EC, reported in five studies, four of which demonstrated a significant positive association, particularly among lean postmenopausal women. In contrast, evidence regarding bisphenol A (BPA) and its metabolites was inconsistent: only mono-n-butyl phthalate (MnBP) showed a positive correlation with EC in one study, while BPA and dibutyl phthalate (DBP) did not. Nonylphenol and octylphenol were also found to be positively associated with EC risk in a single study. Conversely, neither lead exposure nor dietary intake of isoflavones was associated with EC incidence. Overall, available epidemiological evidence supports a potential association between cadmium exposure and increased EC risk, while data for other EDCs remain limited and inconclusive. Substantial heterogeneity in exposure assessment, study design, and confounder adjustment limits comparability across studies and precludes definitive conclusions. Further well-designed longitudinal studies with standardized and repeated exposure measurements are needed to clarify causal relationships between EDC exposure and endometrial carcinogenesis.

https://inplasy.com/inplasy-2025-6-0030/, identifier INPLASY202560030.

## Linked entities

- **Chemicals:** cadmium (PubChem CID 23973), bisphenol A (PubChem CID 6623), mono-n-butyl phthalate (PubChem CID 8575), dibutyl phthalate (PubChem CID 3026), nonylphenol (PubChem CID 1752), octylphenol (PubChem CID 13700), isoflavones (PubChem CID 72304)
- **Diseases:** endometrial cancer (MONDO:0002447)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847], MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, CCND1 (cyclin D1) [NCBI Gene 595] {aka BCL1, D11S287E, PRAD1, U21B31}, MIR149 (microRNA 149) [NCBI Gene 406941] {aka MIRN149, mir-149}, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290] {aka CCM4, CLAPO, CLOVE, CWS5, HMH, MCAP}, CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, GPER1 (G protein-coupled estrogen receptor 1) [NCBI Gene 2852] {aka CEPR, CMKRL2, DRY12, FEG-1, GPCR-Br, GPER}, DBP (D-box binding PAR bZIP transcription factor) [NCBI Gene 1628] {aka DABP, taxREB302}, MIR107 (microRNA 107) [NCBI Gene 406901] {aka MIRN107, miR-107}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, ESR2 (estrogen receptor 2) [NCBI Gene 2100] {aka ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353] {aka AP-1, C-FOS, p55}, NR1I2 (nuclear receptor subfamily 1 group I member 2) [NCBI Gene 8856] {aka BXR, ONR1, PAR, PAR1, PAR2, PARq}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** toxicity (MESH:D064420), EDCs (MESH:D004700), carcinogenic (MESH:D011230), EC (MESH:D016889), deaths (MESH:D003643), polycystic ovary syndrome (MESH:D011085), clear cell (MESH:D002292), hyperplasia (MESH:D006965), endometrial hyperplasia (MESH:D004714), estrogenic (MESH:D056828), Type II tumors (MESH:D009369), endometrioid carcinomas (MESH:D018269), chromosomal aberrations (MESH:D002869), carcinosarcomas (MESH:D002296), mitochondrial dysfunction (MESH:D028361), inflammation (MESH:D007249), hormone-dependent malignancies (MESH:D009376), iron (MESH:D000090463), endometrial carcinogenesis (MESH:D063646), obesity (MESH:D009765)
- **Chemicals:** oil (MESH:D009821), DBP (MESH:D003993), epoxy (MESH:D004853), NP (MESH:C025256), Isoflavones (MESH:D007529), lignan (MESH:D017705), polychlorinated biphenyls (MESH:D011078), Phthalates (MESH:C032279), NA (MESH:D012964), dioxins (MESH:D004147), ISP (-), ROS (MESH:D017382), Cadmium (MESH:D002104), Lead (MESH:D007854), lipid (MESH:D008055), steroid (MESH:D013256), glutathione (MESH:D005978), triazoles (MESH:D014230), OP (MESH:C474055), quercetin (MESH:D011794), E2 (MESH:D004958), MnBP (MESH:C028577), enterolactone (MESH:C029497), BPA (MESH:C006780), triazines (MESH:D014227)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12935642/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935642/full.md

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Source: https://tomesphere.com/paper/PMC12935642