Related Experiment Video
Updated: May 28, 2026

Tropomodulin 3 Overexpression as a Marker for Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
Expression of the opioid growth factor-opioid growth factor receptor axis in human ovarian cancer
James Fanning1, Carrie A Hossler, Joshua P Kesterson
1Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Pennsylvania State University, Milton S. Hershey Medical Center, 500 University Drive, Hershey, PA 17033, USA. jfanning1@hmc.psu.edu
Objective:
The opioid growth factor (OGF) and its receptor (OGFr), serve as inhibitory axis regulating cell proliferation in normal cells and cancer. We investigated the presence and relative expression of OGF and OGFr in normal human ovarian surface epithelial (HOSE) cells, benign ovarian cysts, and ovarian cancers.
Methods:
Surgical samples of 16 patients with ovarian cancer and 27 patients with ovarian benign cysts were obtained intraoperatively. HOSE were collected by scraping the surface of normal ovaries of 10 post menopausal women undergoing hysterectomy and oophorectomy. Semiquantitative immunohistochemistry was used to assess the presence, distribution, and levels of OGF and OGFr. Receptor binding assays measured binding capacity and affinity of OGFr for radiolabeled OGF.
Results:
OGF and OGFr were present in HOSE cells, ovarian cysts, and ovarian cancers. Compared to HOSE cells, OGF and OGFr protein levels were reduced 29% and 34% (p<0.001), respectively, in ovarian cysts, and decreased 58% and 48% (p<0.001), respectively, in ovarian cancers. Binding assays revealed 5.4 fold fewer OGFr binding sites in cancers than cysts (p<0.05). Levels of OGF and OGFr were comparable in primary, metastatic, or recurrent ovarian cancers.
Conclusion:
We have shown that a native opioid pathway, the OGF-OGFr axis, is present in human ovarian cancer. Importantly, the expression of OGF and OGFr is diminished in human ovarian cancer. As OGF and OGFr normally function in maintaining cell proliferation, therapy to harness OGF/OGFr function could provide a useful biologic-based treatment for human ovarian cancer.
Insights
The opioid growth factor (OGF) and its receptor (OGFr) pathway is present in ovarian cancer but diminished. Targeting this OGF-OGFr axis may offer a novel biologic-based therapy for ovarian cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- The opioid growth factor (OGF) and its receptor (OGFr) axis regulates cell proliferation in normal and cancerous cells.
- Understanding the OGF-OGFr pathway in ovarian cancer is crucial for developing new therapeutic strategies.
Purpose of the Study:
- To investigate the presence and relative expression of OGF and OGFr in normal human ovarian surface epithelial (HOSE) cells, benign ovarian cysts, and ovarian cancers.
- To assess the functional binding capacity of OGFr in these tissues.
Main Methods:
- Surgical samples from ovarian cancer (n=16) and benign ovarian cysts (n=27) were analyzed.
- Normal HOSE cells were obtained from postmenopausal women.
- Semiquantitative immunohistochemistry and receptor binding assays were employed to quantify OGF and OGFr levels and binding capacity.
Main Results:
- OGF and OGFr were detected in HOSE cells, ovarian cysts, and ovarian cancers.
- Protein levels of OGF and OGFr were significantly reduced in ovarian cysts and cancers compared to HOSE cells.
- Ovarian cancers exhibited significantly fewer OGFr binding sites compared to benign cysts.
Conclusions:
- The OGF-OGFr axis is present in human ovarian cancer, but its expression is diminished.
- The reduced expression of OGF and OGFr suggests a potential therapeutic target.
- Harnessing the OGF-OGFr pathway could lead to novel biologic-based treatments for ovarian cancer.
More Related Videos
Related Concept Videos
Mitogens and the Cell Cycle
Opioid Receptors: Overview
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Hormonal Control of the Ovarian Cycle
Before puberty, the hypothalamus releases GnRH in a low frequency, low amplitude pulsatile manner. This along with the immature hypothalamic-pituitary-gonadal axis activity, results in low estrogen levels and the absence of a fully functional ovarian cycle. At puberty, GnRH secretion increases in both frequency and...

