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Modeling the Early Steps of Ovarian Cancer Dissemination in an Organotypic Culture of the Human Peritoneal Cavity
Published on: December 31, 2015
Extracellular matrix of ovarian tumors
Carmela Ricciardelli1, Raymond J Rodgers
1Research Centre for Reproductive Health, Discipline of Obstetrics and Gynaecology, School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, South Australia, Australia. carmela.ricciardelli@adelaide.edu.au
Abstract:
Tumor cells interfere with the normal programming of extracellular matrix (ECM) biosynthesis and can extensively modify the structure and composition of the matrix. The role of ECM components is becoming increasingly recognized as an important determinant for the growth and progression of solid tumors. The extensive remodeling of the normal ECM in tumors can proceed through the degradation of pre-existing ECM molecules and/or by the neosynthesis of ECM components, which in many cases are not present in the ECM of normal tissues. In the ovary the ECM comprises a variety of molecules including the collagen superfamily and noncollagenous proteins such as glycoproteins, proteoglycans, and hyaluronan. Elevated levels of laminin-gamma2, collagen types I and III, fibronectin, syndecan-1, glypican-1, versican, and hyaluronan and its receptors CD44 have all been associated with a poor prognosis of ovarian cancers. Generally, there is a differential expression of laminin chains alpha1, alpha4, and beta2 among serous (alpha1, beta2), mucinous (alpha4), and endometrioid (alpha1) tumors. This review focuses on these and other ECM molecules in ovarian tumors.
Insights
Tumor cells alter the ovarian extracellular matrix (ECM), impacting cancer growth. Specific ECM molecules are linked to poor ovarian cancer prognosis, highlighting their role in disease progression.
Area of Science:
- Oncology
- Biochemistry
- Molecular Biology
Background:
- Tumor cells extensively modify the extracellular matrix (ECM) structure and composition.
- ECM remodeling, through degradation and neosynthesis, influences solid tumor growth and progression.
- The ovarian ECM includes collagens, glycoproteins, proteoglycans, and hyaluronan.
Purpose of the Study:
- To review the role of ECM molecules in ovarian tumors.
- To highlight specific ECM components associated with poor prognosis in ovarian cancer.
- To discuss the differential expression of laminin chains in various ovarian tumor types.
Main Methods:
- Literature review of studies on ECM in ovarian cancer.
- Analysis of ECM component expression and prognostic significance.
- Comparison of ECM composition across different ovarian tumor subtypes.
Main Results:
- Elevated levels of laminin-gamma2, collagen types I and III, fibronectin, syndecan-1, glypican-1, versican, and hyaluronan/CD44 are linked to poor ovarian cancer prognosis.
- Differential expression of laminin chains (alpha1, alpha4, beta2) is observed among serous, mucinous, and endometrioid ovarian tumors.
- ECM remodeling is a key factor in ovarian tumor progression.
Conclusions:
- ECM components are critical determinants of ovarian cancer growth and progression.
- Specific ECM molecules and their altered expression patterns serve as potential prognostic markers for ovarian cancer.
- Targeting ECM remodeling may offer therapeutic strategies for ovarian cancer.
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