The hallmarks of ovarian cancer: proliferation and cell growth

Epithelial ovarian cancer (EOC) is a heterogeneous group of diseases with distinct biological and clinical behaviour. Despite the differences between them, the capability of tumour cells to continuously proliferate and avoid death is maintained among histotypes. This ability is the result of alterat...

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Main Authors: Raquel López-Reig, José Antonio López-Guerrero
Format: Article
Language:English
Published: Elsevier 2020-08-01
Series:EJC Supplements
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1359634919300060
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spelling doaj-cde4487b39554eabbd67d95bd634420c2020-11-25T03:27:45ZengElsevierEJC Supplements1359-63492020-08-01152737The hallmarks of ovarian cancer: proliferation and cell growthRaquel López-Reig0José Antonio López-Guerrero1Laboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología (IVO), 46009 Valencia, Spain; IVO-CIPF Joint Research Unit of Cancer, Príncipe Felipe Research Center (CIPF), 46012 Valencia, SpainLaboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología (IVO), 46009 Valencia, Spain; Department of Basic Medical Sciences, School of Medicine, Catholic University of Valencia ‘San Vicente Martir’, 46001 Valencia, Spain; Corresponding author: Laboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, C/Prof. Beltrán Báguena, 8-11, Valencia, Spain.Epithelial ovarian cancer (EOC) is a heterogeneous group of diseases with distinct biological and clinical behaviour. Despite the differences between them, the capability of tumour cells to continuously proliferate and avoid death is maintained among histotypes. This ability is the result of alterations at different levels, causing the deregulation of cell cycle and proliferative-related pathways. Even if the leading role is played by RB and TP53, changes in other molecular pathways are involved in the development of EOC. This ability can be exploited to generate in vitro and in vivo models resembling the conditions of tumour development in a patient. In vivo models, such as patient-derived xenografts (PDX) or genetically engineered mouse models (GEMM), represent a fundamental tool in the study of the molecular mechanisms implicated in each EOC biotype for testing new therapeutic approaches. Herein we describe the major proliferation-related pathways and its disruption found in EOC and how these features can be used to establish in vivo models for translational research.http://www.sciencedirect.com/science/article/pii/S1359634919300060Epithelial ovarian cancerCell proliferationCell growthAnimal models
collection DOAJ
language English
format Article
sources DOAJ
author Raquel López-Reig
José Antonio López-Guerrero
spellingShingle Raquel López-Reig
José Antonio López-Guerrero
The hallmarks of ovarian cancer: proliferation and cell growth
EJC Supplements
Epithelial ovarian cancer
Cell proliferation
Cell growth
Animal models
author_facet Raquel López-Reig
José Antonio López-Guerrero
author_sort Raquel López-Reig
title The hallmarks of ovarian cancer: proliferation and cell growth
title_short The hallmarks of ovarian cancer: proliferation and cell growth
title_full The hallmarks of ovarian cancer: proliferation and cell growth
title_fullStr The hallmarks of ovarian cancer: proliferation and cell growth
title_full_unstemmed The hallmarks of ovarian cancer: proliferation and cell growth
title_sort hallmarks of ovarian cancer: proliferation and cell growth
publisher Elsevier
series EJC Supplements
issn 1359-6349
publishDate 2020-08-01
description Epithelial ovarian cancer (EOC) is a heterogeneous group of diseases with distinct biological and clinical behaviour. Despite the differences between them, the capability of tumour cells to continuously proliferate and avoid death is maintained among histotypes. This ability is the result of alterations at different levels, causing the deregulation of cell cycle and proliferative-related pathways. Even if the leading role is played by RB and TP53, changes in other molecular pathways are involved in the development of EOC. This ability can be exploited to generate in vitro and in vivo models resembling the conditions of tumour development in a patient. In vivo models, such as patient-derived xenografts (PDX) or genetically engineered mouse models (GEMM), represent a fundamental tool in the study of the molecular mechanisms implicated in each EOC biotype for testing new therapeutic approaches. Herein we describe the major proliferation-related pathways and its disruption found in EOC and how these features can be used to establish in vivo models for translational research.
topic Epithelial ovarian cancer
Cell proliferation
Cell growth
Animal models
url http://www.sciencedirect.com/science/article/pii/S1359634919300060
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