Human Cytomegalovirus Suppresses Estrogen and Progesterone Receptor Expression in Hormone Receptor-Positive Breast

Erica C Garcia1,2, Ian J LaRue1, Nathan D Griggs1

  • 1Division of Biology, Texas Woman's University, Denton, TX 76204, USA.

Cancers
|August 13, 2026
PubMed
Abstract

Insights

Human cytomegalovirus (HCMV) exposure reduces estrogen receptor-alpha (ERα) and progesterone receptor (PR) in breast cancer cells. This effect occurs independently of viral replication, suggesting HCMV influences hormone signaling pathways.

Area of Science:

  • Oncology
  • Virology
  • Molecular Biology

Background:

  • Hormone receptor-positive breast cancer relies on estrogen and progesterone signaling.
  • Factors influencing hormone receptor expression in tumors are not fully understood.
  • Human cytomegalovirus (HCMV) is found in breast tumors and linked to reduced ERα and PR, but causality is unproven.

Purpose of the Study:

  • To investigate the causal relationship between HCMV infection and hormone receptor expression in breast cancer.
  • To determine if viral replication is necessary for HCMV to affect ERα and PR levels.

Main Methods:

  • Infection of ER+/PR+ breast cancer cell lines (MCF-7, T47D) with HCMV in vitro.
  • Assessment of ERα and PR protein levels via immunoblotting.
  • Quantification of ESR1 and PGR transcript levels using qPCR.
  • Use of UV-inactivated HCMV to test the role of viral replication.

Main Results:

  • HCMV infection significantly reduced ERα and PR protein levels in both cell lines.
  • Decreased ESR1 and PGR transcript levels were observed 48 hours post-infection.
  • UV-inactivated HCMV caused similar suppression, indicating viral replication is not required.

Conclusions:

  • HCMV exposure suppresses ERα and PR expression in breast cancer cells via a replication-independent mechanism.
  • Viral components or host responses to HCMV may alter tumor hormone receptor signaling.
  • HCMV is identified as a potential modulator of hormone receptor pathways in breast cancer, impacting endocrine therapy responsiveness.

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