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Oogenesis02:07

Oogenesis

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In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from the equivalent procedure of spermatogenesis in males. First, meiotic divisions during oogenesis are asymmetric, meaning that a large oocyte (containing most of the cytoplasm) and minor polar body are produced as a result of meiosis I, and again following meiosis II. Since only oocytes will go on to form embryos if fertilized, this unequal...
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Evaluating the Angiogenetic Properties of Ovarian Cancer Stem-Like Cells using the Three-Dimensional Co-Culture System, NICO-1
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Advanced Glycation End Products as a Potential Target for Restructuring the Ovarian Cancer Microenvironment: A Pilot

Elizabeth I Harper1,2,3, Michael D Siroky2,3, Tyvette S Hilliard2,3

  • 1Integrated Biomedical Sciences Graduate Program, University of Notre Dame, Notre Dame, IN 46556, USA.

International Journal of Molecular Sciences
|June 28, 2023
PubMed
Summary

Advanced glycation end products (AGEs) contribute to ovarian cancer progression in older women. This study explores AGE breakers, showing their potential to alter the tumor microenvironment and improve treatment response.

Keywords:
AGE breakersALT-711Alagebriumadvanced glycation end product (AGE)collagenmicroenvironmentomentumovarian cancer

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Area of Science:

  • Oncology
  • Gerontology
  • Biochemistry

Background:

  • Ovarian cancer is a leading cause of cancer death in women, particularly those over 60.
  • Age-related changes in the tumor microenvironment, such as advanced glycation end products (AGEs) crosslinking collagen, promote metastasis.
  • The therapeutic potential of AGE breakers in ovarian cancer remains unexplored.

Purpose of the Study:

  • To investigate the efficacy of AGE breakers in targeting age-related changes in the ovarian cancer microenvironment.
  • To assess the potential of AGE breakers to improve treatment response in older ovarian cancer patients.

Main Methods:

  • Pilot study evaluating AGE breakers.
  • Analysis of changes in omental collagen structure.
  • Modulation of the peritoneal immune landscape.

Main Results:

  • AGE breakers demonstrated the potential to alter omental collagen structure.
  • AGE breakers showed capacity to modulate the peritoneal immune landscape.

Conclusions:

  • AGE breakers may represent a novel therapeutic strategy for ovarian cancer.
  • Targeting AGEs could improve treatment outcomes for older ovarian cancer patients.