Autocrine stimulation of clear-cell renal carcinoma cell migration in hypoxia via HIF-independent suppression of thrombospondin-1

Thrombospondin-1 is a matricellular protein with potent antitumour activities, the levels of which determine the fate of many different tumours, including renal carcinomas. However, the factors that regulate this protein remain unclear. In renal carcinomas, hypoxic conditions enhance the expression...

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Detalhes bibliográficos
Autores: Bienes-Martínez, Raquel, Ordóñez, Angel, Feijoo-Cuaresma, Mónica, Corral-Escariz, María, Mateo, Gloria, Stenina, Olga, Jiménez Cuenca, Benilde, Calzada García, María Josefa
Tipo de documento: artigo
Data de publicação:2012
País:España
Recursos:Universidad Autónoma de Madrid
Repositório:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglês
OAI Identifier:oai:repositorio.uam.es:10486/668536
Acesso em linha:http://hdl.handle.net/10486/668536
https://dx.doi.org/10.1038/srep00788
Access Level:Acceso aberto
Palavra-chave:Cancer microenvironment
Tumour suppressors
Tumor angiogenesis
Oncogenesis
Medicina
Descrição
Resumo:Thrombospondin-1 is a matricellular protein with potent antitumour activities, the levels of which determine the fate of many different tumours, including renal carcinomas. However, the factors that regulate this protein remain unclear. In renal carcinomas, hypoxic conditions enhance the expression of angiogenic factors that help adapt tumour cells to their hostile environment. Therefore, we hypothesized that anti-angiogenic factors should correspondingly be dampened. Indeed, we found that hypoxia decreased the thrombospondin-1 protein in several clear cell renal carcinoma cell lines (ccRCC), although no transcriptional regulation was observed. Furthermore, we proved that hypoxia stimulates multiple signals that independently contribute to diminish thrombospondin-1 in ccRCC, which include a decrease in the activity of oxygen-dependent prolylhydroxylases (PHDs) and activation of the PI3K/Akt signalling pathway. In addition, thrombospondin-1 regulation in hypoxia proved to be important for ccRCC cell migration and invasion