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Updated: Jul 14, 2026

Isolation of Human Endometrial Stromal Cells for In Vitro Decidualization
Published on: September 1, 2018
Clinical implications of steroid receptor coactivator (SRC)-3 in uterine endometrial cancers
Hideki Sakaguchi1, Jiro Fujimoto, Wen-Shu Sun
1Department of Obstetrics and Gynecology, Gifu University School of Medicine, 1-1 Yanagido, Gifu City 501-1194, Japan. gucci555@nifty.com
Abstract:
Estrogen is recognized as a significant modifier in the development, growth and invasion of uterine endometrial cancer. Steroid receptor coactivator-3 (SRC-3; AIB1, ACTR, RAC3, TRAM-1, and pCIP) is a member of the p160 family of coactivator for nuclear hormone receptors including estrogen receptor (ER). It is reported that SRC-3 is overexpressed in various cancers. However, SRC-3 expression manner in uterine endometrial cancer is not fully understood. In this study, we showed SRC-3 mRNA expression correlates with clinical stage, depth of myometrial invasion and dedifferentiation. The prognosis of the 25 patients with higher expression of SRC-3 mRNA in uterine endometrial cancers was extremely poor (36%), whereas the 24-month survival rate of the 15 patients with lower expression of SRC-3 mRNA was 96%. These data indicate that SRC-3 might be an important indicator of uterine endometrial cancer advancement and survival.
Insights
Steroid receptor coactivator-3 (SRC-3) mRNA levels indicate uterine endometrial cancer progression. Higher SRC-3 expression correlates with poor prognosis and advanced disease stages.
Area of Science:
- Oncology
- Molecular Biology
- Gynecologic Oncology
Background:
- Estrogen significantly influences uterine endometrial cancer development, growth, and invasion.
- Steroid receptor coactivator-3 (SRC-3) is a coactivator for estrogen receptors and is overexpressed in various cancers.
- The expression pattern and clinical significance of SRC-3 in uterine endometrial cancer remain incompletely understood.
Purpose of the Study:
- To investigate the expression of SRC-3 mRNA in uterine endometrial cancer.
- To determine the correlation between SRC-3 mRNA levels and clinicopathological features.
- To evaluate the prognostic value of SRC-3 mRNA expression in uterine endometrial cancer patients.
Main Methods:
- Quantitative analysis of SRC-3 mRNA expression in uterine endometrial cancer tissues.
- Correlation analysis between SRC-3 mRNA levels and clinical stage, myometrial invasion depth, and tumor differentiation.
- Survival analysis comparing patients with high versus low SRC-3 mRNA expression.
Main Results:
- SRC-3 mRNA expression was found to correlate with clinical stage, depth of myometrial invasion, and dedifferentiation.
- Patients with higher SRC-3 mRNA expression exhibited a significantly poorer prognosis (36% 24-month survival).
- Patients with lower SRC-3 mRNA expression had a much better 24-month survival rate (96%).
Conclusions:
- SRC-3 mRNA expression is closely associated with the advancement of uterine endometrial cancer.
- SRC-3 may serve as a valuable prognostic biomarker for uterine endometrial cancer.
- Targeting SRC-3 could potentially offer therapeutic strategies for improving patient survival.
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