Abstract
We recently proposed to formally recognize Key Event Relationships (KERs) as building blocks of Adverse Outcome Pathways (AOPs) that can be independently developed and peer-reviewed. Here, we follow this approach and provide an independent KER from AOP345, which describes androgen receptor (AR) antagonism leading to decreased female fertility. This KER connects AR antagonism to reduced granulosa cell proliferation of gonadotropin-independent follicles (KER2273). We have developed both the KER and the two adjacent Key Events (KEs). A systematic approach was used to ensure that all relevant supporting evidence for KER2273 was retrieved. Supporting evidence for the KER highlights the importance of AR action during the early stages of follicular development. Both biological plausibility and empirical evidence are presented, with the latter also assessed for quality. We believe that tackling isolated KERs instead of whole AOPs will accelerate the AOP development. Faster AOP development will lead to the development of simple test methods that will aid screening of chemicals, endocrine disruptor identification, risk assessment, and subsequent regulation.
| Original language | English |
|---|---|
| Journal | Reproductive Toxicology |
| Volume | 112 |
| Pages (from-to) | 136-147 |
| Number of pages | 12 |
| ISSN | 0890-6238 |
| DOIs | |
| Publication status | Published - 2022 |
Keywords
- Adverse Outcome Pathway
- Key Event Relationship
- Androgen Receptor
- Ovary Ovarian follicle
- Folliculogenesis
- Granulosa cell
- Fertility
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