Associations between Exposure to Organochlorine Chemicals and Endometriosis: A Systematic Review of Experimental Studies and Integration of Epidemiological Evidence
Growing epidemiological evidence suggests that organochlorine chemicals (OCCs), including 2,3,7,8-tetrachlorodibenzo- -dioxin (TCDD), may play a role in the pathogenesis of endometriosis. We aimed to systematically review the experimental evidence ( and ) on the associations between exposure to OCCs...
Gespeichert in:
Veröffentlicht in: | Environmental health perspectives 2021-07, Vol.129 (7), p.76003-76003 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Growing epidemiological evidence suggests that organochlorine chemicals (OCCs), including 2,3,7,8-tetrachlorodibenzo-
-dioxin (TCDD), may play a role in the pathogenesis of endometriosis.
We aimed to systematically review the experimental evidence (
and
) on the associations between exposure to OCCs and endometriosis-related end points.
A systematic review protocol was developed following the National Toxicology Program /Office of Health Assessment and Translation (NTP/OHAT) framework and managed within a web-based interface.
studies designed to evaluate the impact of OCCs on the onset or progression of endometriosis and proliferation of induced endometriotic lesions were eligible. Eligible
studies included single-cell and co-culture models to evaluate the proliferation, migration, and/or invasion of endometrial cells. We applied the search strings to PubMed, Web of Science, and Scopus®. A final search was performed on 24 June 2020. Assessment of risk of bias and the level of evidence and integration of preevaluated epidemiological evidence was conducted using NTP/OHAT framework Results: Out of 812 total studies, 39 met the predetermined eligibility criteria (15
, 23
, and 1 both). Most studies (
) tested TCDD and other dioxin-like chemicals.
evidence supported TCDD's promotion of endometriosis onset and lesion growth.
evidence supported TCDD's promotion of cell migration and invasion, but there was insufficient evidence for cell proliferation.
evidence further supported the roles of the aryl hydrocarbon receptor and matrix metalloproteinases in mediating steroidogenic disruption and inflammatory responses. Estrogen interactions were found across studies and end points.
Based on the integration of a high level of animal evidence with a moderate level of epidemiological evidence, we concluded that TCDD was a known hazard for endometriosis in humans and the conclusion is supported by mechanistic
evidence. Nonetheless, there is need for further research to fill in our gaps in understanding of the relationship between OCCs and their mixtures and endometriosis, beyond the prototypical TCDD. https://doi.org/10.1289/EHP8421. |
---|---|
ISSN: | 0091-6765 1552-9924 |
DOI: | 10.1289/EHP8421 |