# Dexamethasone Suppresses Already Low Estrogen Receptor Levels in Meningiomas

**Authors:** Judith C. Hugh, Lacey S. J. Haddon, John Maringa Githaka

PMC · DOI: 10.3390/ijms27062779 · International Journal of Molecular Sciences · 2026-03-19

## TL;DR

Dexamethasone may be reducing already low estrogen receptor levels in meningiomas, which could affect hormone-related treatment approaches.

## Contribution

The study suggests that dexamethasone suppresses estrogen receptor levels in meningiomas, explaining their low ER positivity.

## Key findings

- Ligand-binding assays showed a significant decrease in estrogen receptor positivity after 1984.
- Dexamethasone exposure was confirmed to be associated with reduced ER levels in 93 patients.
- ER+ cells in meningiomas are rare and unrelated to PR and pS2 expression, consistent with Dex inhibition.

## Abstract

Intracranial meningiomas (ICMs) are the most common primary adult brain tumor. They are more frequent in women, respond to female hormones, are associated with breast cancer and are often progesterone receptor-positive (PR+), consistent with hormonal sensitivity. Yet <20% are weakly estrogen receptor-positive (ER+). This work reviews the literature to investigate this paucity of ER by first testing if Dexamethasone (Dex), which has been used since 1984 to reduce peritumoral brain edema, is suppressing ER. Ligand-binding assays after 1984 have shown a significant decrease in any and supra-threshold (>10 fmol/mg) ER+ from 68.5% and 39.6% to 25.5% and 12%, respectively (both p < 0.0001). This was confirmed as Dex-related in 93 patients with known Dex exposure (p = 0.0075). Immunohistochemical tests after 1984 have shown that 16% (95%CI 8.4–24.4) of ICMs have rare ER+ cells unrelated to PR and pS2 expression, consistent with Dex inhibition of ER transcription activity. Dex suppression of ER may be compounded by lower endogenous ER concentrations in ICMs compared to breast cancer. The difference in intra-tumoral estrogen concentration is proposed as a potential cause for lower ER in ICM. Replacement of Dex and more sensitive ER assays are needed to determine the role of hormones in the causation and treatment of ER+ ICM.

## Linked entities

- **Proteins:** PSEN2 (presenilin 2)
- **Chemicals:** Dexamethasone (PubChem CID 5743), estrogen (PubChem CID 12115739)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** TAS2R64P (taste 2 receptor member 64, pseudogene) [NCBI Gene 338412] {aka PS2, T2R64, T2R64P}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}
- **Diseases:** brain tumor (MESH:D001932), brain edema (MESH:D001929), breast cancer (MESH:D001943), ICMs (MESH:D008579)
- **Chemicals:** Dex (MESH:D003907)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

151 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026750/full.md

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Source: https://tomesphere.com/paper/PMC13026750