Related Experiment Video
Updated: Apr 27, 2026

A Kinetic Fluorescence-based Ca2+ Mobilization Assay to Identify G Protein-coupled Receptor Agonists, Antagonists, and Allosteric Modulators
Published on: February 20, 2018
Consideration of GREB1 as a potential therapeutic target for hormone-responsive or endocrine-resistant cancers
Kendra M Hodgkinson1, Barbara C Vanderhyden
1Ottawa Hospital Research Institute, Centre for Cancer Therapeutics , 501 Smyth Road, 3rd Floor, Box 926, Ottawa, Ontario K1H 8L6 , Canada.
Introduction:
Steroid hormones increase the incidence and promote the progression of many types of cancer. Exogenous estrogens increase the risk of developing breast, ovarian and endometrial cancer and many breast cancers initially respond to estrogen deprivation. Although steroid hormone signaling has been extensively studied, the mechanisms of hormone-stimulated cancer growth have not yet been fully elucidated, limiting opportunities for novel approaches to therapeutic intervention.
Areas Covered:
This review examines growing evidence for the important role played by the steroid hormone-induced gene called GREB1, or growth regulation by estrogen in breast cancer 1. GREB1 is a critical mediator of both the estrogen-stimulated proliferation of breast cancer cells and the androgen-stimulated proliferation of prostate cancer cells.
Expert Opinion:
Although its exact function in the cascade of hormone action remains unclear, the ability of GREB1 to modulate tumor progression in models of breast, ovarian and prostate cancer renders this gene an excellent candidate for further consideration as a potential therapeutic target. Research examining the mechanism of GREB1 action will help to elucidate its role in proliferation and its potential contribution to endocrine resistance and will determine whether GREB1 interference may have therapeutic efficacy.
Insights
Growth Regulation by Estrogen (GREB1) is a key gene in hormone-driven cancers like breast and prostate. Understanding GREB1's role may lead to new therapeutic strategies targeting cancer progression.
Area of Science:
- Oncology
- Molecular Biology
- Endocrinology
Background:
- Steroid hormones significantly influence cancer incidence and progression.
- Estrogen exposure increases risks for breast, ovarian, and endometrial cancers.
- Mechanisms of hormone-stimulated cancer growth require further elucidation for novel therapies.
Purpose of the Study:
- To review the role of the Growth Regulation by Estrogen 1 (GREB1) gene.
- To examine GREB1 as a mediator of estrogen and androgen signaling in cancer.
Main Methods:
- Literature review of studies on GREB1 function.
- Analysis of GREB1's role in hormone-stimulated cell proliferation.
Main Results:
- GREB1 is induced by steroid hormones.
- GREB1 mediates estrogen-stimulated breast cancer cell proliferation.
- GREB1 mediates androgen-stimulated prostate cancer cell proliferation.
Conclusions:
- GREB1 is a critical mediator in hormone-driven cancers.
- GREB1 modulates tumor progression in breast, ovarian, and prostate cancer models.
- GREB1 is a potential therapeutic target for endocrine resistance and cancer treatment.
More Related Videos
07:03Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
Published on: October 2, 2020
08:59Looking for Driver Pathways of Acquired Resistance to Targeted Therapy: Drug Resistant Subclone Generation and Sensitivity Restoring by Gene Knock-down
Published on: December 11, 2017
Related Concept Videos
Mitogens and the Cell Cycle
Targeted Cancer Therapies
There are several types of targeted therapies against...
G Protein-coupled Receptors
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
Transducer Mechanism: Enzyme-Linked Receptors
Major types that are helpful drug targets include:
Treatment Resistant Cancers
Abnormal Proliferation