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Updated: Jun 4, 2026

Transplantation Into the Mouse Ovarian Fat Pad
Published on: September 7, 2016
New players in ovarian cancer
Alessandro Bovicelli1, Giuseppina D'Andrilli, Antonio Giordano
1Sbarro Institute for Cancer Research and Molecular Medicine, Center for Biotechnology, College of Science and Technology, Temple University, Philadelphia, PA 19122, USA.
Abstract:
Ovarian cancer is the leading cause of gynecologic cancer mortality worldwide. The aim of this review is to highlight the most recent studies regarding ovarian cancer pathogenesis and the new therapeutic approaches against this insidious disease. We focus on the relevance of some cell cycle genes, transcription factors, and microRNAs in the carcinogenesis of ovarian cancer as well as on a new hypothesis for therapy using histone deacetylase inhibitors. We also report recent studies regarding some mechanisms of chemoresistance, a major obstacle in the treatment of ovarian cancer. Together these studies can improve our knowledge of ovarian cancer tumorigenesis and diagnosis providing new tools to hopefully defeat this deadly disease.
Insights
This review explores ovarian cancer (OC) pathogenesis, focusing on cell cycle genes, transcription factors, and microRNAs. It highlights new therapeutic strategies, including histone deacetylase inhibitors, and chemoresistance mechanisms to improve OC diagnosis and treatment.
Area of Science:
- Gynecologic Oncology
- Molecular Biology
- Cancer Genetics
Background:
- Ovarian cancer (OC) is the leading cause of gynecologic cancer mortality globally.
- Understanding OC pathogenesis is crucial for developing effective treatments.
- Chemoresistance remains a significant challenge in managing OC.
Purpose of the Study:
- To review recent studies on ovarian cancer pathogenesis.
- To highlight novel therapeutic approaches for OC.
- To discuss the role of specific genes, microRNAs, and histone deacetylase inhibitors in OC.
Main Methods:
- Literature review of recent studies on ovarian cancer.
- Analysis of cell cycle genes, transcription factors, and microRNAs in carcinogenesis.
- Evaluation of histone deacetylase inhibitors as a therapeutic hypothesis.
- Review of mechanisms contributing to chemoresistance in OC.
Main Results:
- Recent studies implicate cell cycle genes, transcription factors, and microRNAs in OC development.
- Histone deacetylase inhibitors present a promising new therapeutic avenue.
- Understanding chemoresistance mechanisms is vital for treatment efficacy.
- Advances in knowledge can improve OC diagnosis and patient outcomes.
Conclusions:
- Recent research offers insights into OC tumorigenesis and potential therapeutic targets.
- Novel strategies, including epigenetic modifiers, show promise against OC.
- Addressing chemoresistance is key to improving survival rates for ovarian cancer patients.
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