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

Gynecologic Oncology
|November 1, 2011
PubMed
Abstract

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.

Related Concept Videos

Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
Opioid Receptors: Overview01:22

Opioid Receptors: Overview

Opioid receptors, including the mu (μ, MOR), delta (δ, DOR), and kappa (κ, KOR) types, belong to the rhodopsin family of G protein-coupled receptors. These receptors are located throughout the central and peripheral nervous systems and in non-neuronal tissues such as macrophages and astrocytes. Opioid receptor ligands can be categorized into agonists or antagonists. Highly selective agonists include [d-Ala2, MePhe4, Gly(ol)5]-enkephalin or DAMGO for MOR, [D-Pen2, D-Pen5]-enkephalin or DPDPE for...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
Hormonal Control of the Ovarian Cycle01:30

Hormonal Control of the Ovarian Cycle

The ovarian cycle is meticulously regulated by the hypothalamic-pituitary-gonadal axis. This cycle orchestrates the release of a mature oocyte, essential for reproduction.
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...