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Updated: Dec 25, 2025

Tubal Cytology of the Fallopian Tube as a Promising Tool for Ovarian Cancer Early Detection
Published on: July 25, 2017
The tubal epigenome - An emerging target for ovarian cancer
Hunter D Reavis1, Ronny Drapkin2
1Penn Ovarian Cancer Research Center, Department of Obstetrics and Gynecology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA; Graduate Program in Cell and Molecular Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA; Department of Cancer Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Abstract:
Ovarian cancer is the most lethal gynecologic malignancy in the United States. The mortality of this disease is primarily attributed to challenges in early detection and therapeutic resistance. Recent studies indicate that the majority of high-grade serous ovarian carcinomas (HGSCs) originate from aberrant fallopian tube epithelial (FTE) cells. This shift in thinking about ovarian cancer pathogenesis has been met with an effort to identify the early genetic and epigenetic changes that underlie the transformation of normal FTE cells and prompt them to migrate and colonize the ovary, ultimately giving rise to aggressive HGSC. While identification of these early changes is important for biomarker discovery, the emergence of epigenetic alterations in FTE chromatin may also provide new opportunities for early detection, prevention, and therapeutic intervention. Here we provide a comprehensive overview of the current knowledge regarding early epigenetic reprogramming that precedes HGSC tumor development, the way that these alterations affect both intrinsic and extrinsic tumor properties, and how the epigenome may be targeted to thwart HGSC tumorigenesis.
Insights
Epigenetic alterations in fallopian tube epithelial cells precede high-grade serous ovarian carcinoma (HGSC) development. Targeting these epigenetic changes offers new avenues for early detection, prevention, and treatment of ovarian cancer.
Area of Science:
- Gynecologic Oncology
- Epigenetics
- Molecular Pathology
Background:
- Ovarian cancer, particularly high-grade serous ovarian carcinoma (HGSC), is a leading cause of cancer mortality in the United States.
- Mortality is driven by difficulties in early detection and the development of therapeutic resistance.
- Emerging evidence suggests HGSC originates from aberrant fallopian tube epithelial (FTE) cells.
Purpose of the Study:
- To provide a comprehensive overview of early epigenetic reprogramming in FTE cells preceding HGSC.
- To examine how these epigenetic alterations influence intrinsic and extrinsic tumor properties.
- To explore the potential of targeting the epigenome for HGSC prevention and treatment.
Main Methods:
- Literature review and synthesis of current research on epigenetic alterations in FTE cells.
- Analysis of studies investigating the link between epigenetic changes and HGSC pathogenesis.
- Exploration of therapeutic strategies targeting epigenetic modifications.
Main Results:
- Epigenetic reprogramming in FTE cells is a critical early event in HGSC development.
- These epigenetic alterations impact cellular behavior, promoting migration and colonization.
- The epigenome presents a promising target for novel therapeutic interventions and early detection biomarkers.
Conclusions:
- Understanding early epigenetic changes in FTE cells is crucial for deciphering HGSC origins.
- Targeting epigenetic modifications in FTE cells holds significant potential for preventing and treating HGSC.
- Epigenetic strategies may overcome current challenges in ovarian cancer management.
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