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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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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