Evidence map›Paper›PMID 42588734›Full record

ArticleCancers2026

Human Cytomegalovirus Suppresses Estrogen and Progesterone Receptor Expression in Hormone Receptor-Positive Breast Cancer Cells: Implications for Endocrine Resistance.

Erica C Garcia, Ian J LaRue, Nathan D Griggs, Juliet V Spencer

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Erica C GarciaDivision of Biology, Texas Woman's University, Denton, TX 76204, USA.ORCID 0009-0001-8977-893X
Ian J LaRueDivision of Biology, Texas Woman's University, Denton, TX 76204, USA.
Nathan D GriggsDivision of Biology, Texas Woman's University, Denton, TX 76204, USA.
Juliet V SpencerDivision of Biology, Texas Woman's University, Denton, TX 76204, USA.ORCID 0000-0003-0778-6408

Funding

Texas Woman's University Biology Faculty Development Funds 2022-2024Texas Woman's University Jane Nelson Institute for Women's Leadership 2021Texas Woman's University Paup Foundation Fellowship 2022-2024Texas Woman's University REP 2022
6 · The paper itself

Abstract

backgroundHormone receptor-positive breast cancer depends on estrogen and progesterone signaling, yet factors that modulate hormone receptor expression within tumors remain incompletely understood. Human cytomegalovirus (HCMV), a widespread herpesvirus detected in breast tumors, has been associated with reduced expression of estrogen receptor-α (ERα) and progesterone receptor (PR), but a direct causal relationship has not been established.

methodsER+/PR+ breast cancer cell lines MCF-7 and T47D were infected with HCMV in vitro. ERα and PR protein levels were assessed by immunoblotting, and transcript levels of

resultsHCMV infection resulted in a marked reduction in ERα and PR protein levels in both cell lines, accompanied by decreased

conclusionsThese findings indicate that HCMV exposure suppresses ERα and PR expression in breast cancer cells through a replication-independent mechanism. This effect suggests that viral components or host responses to infection may alter hormone receptor signaling within tumors, with potential implications for hormone receptor signaling and endocrine therapy responsiveness that warrant further investigation. Together, these results identify HCMV as a previously underrecognized modulator of hormone receptor pathways in breast cancer.

Indexed as

breast cancerestrogen receptor-α (ER-α)hormone receptor (HR)hormone therapyHuman Cytomegalovirus (HCMV)Human Herpesvirus 5progesterone receptor (PR)

Identifiers

PMID42588734
PMCPMC13464808

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.