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<dc:title xml:lang="fr">Rôle de MUC1 en physiopathologie rénale : cancer et inflammation</dc:title>
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<dc:subject xml:lang="fr">MUC1</dc:subject>
<dc:subject xml:lang="fr">Chimiorésistance</dc:subject>
<dc:subject xml:lang="fr">Carcinome rénal</dc:subject>
<dc:subject xml:lang="fr">Inflammation</dc:subject>
<dc:subject xml:lang="en">MUC1</dc:subject>
<dc:subject xml:lang="en">Chemoresistance</dc:subject>
<dc:subject xml:lang="en">Renal cell carcinoma</dc:subject>
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<tef:elementdEntree autoriteExterne="040676811" autoriteSource="Sudoc.FMesh">Néphrocarcinome</tef:elementdEntree>
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<tef:elementdEntree autoriteExterne="04069688X" autoriteSource="Sudoc.FMesh">Résistance aux substances</tef:elementdEntree>
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<dcterms:abstract xml:lang="fr">La mucine membranaire MUC1 est surexprimée dans 65% des cancers épithéliaux et hématologiques. Cette surexpression est associée à un mauvais pronostic et à une chimiorésistance, en particulier dans le carcinome rénal. Les travaux de l'équipe ont montré que dans les cellules cancéreuses rénales, la surexpression de MUC1 est corrélée avec l'acquisition des propriétés caractéristiques des cellules cancéreuses (prolifération, migration, invasion, métastase) et la progression tumorale. Ce projet a pour but d'élucider les mécanismes par lesquels MUC1 induit la cancérogenèse épithéliale rénale et la chimiorésistance. Nous envisageons ensuite d'en faire une cible thérapeutique et ainsi développer de potentielles molécules, afin d'élargir le panel de thérapies à disposition des cliniciens.</dcterms:abstract>
<dcterms:abstract xml:lang="en">The membrane-bound mucin MUC1 is overexpressed in 65% of epithelial and haematological cancers. This overexpression is correlated with poor prognosis and chemoresistance, in particular in renal cell carcinoma. Previous results in the team showed that in renal cancer cells, overexpression of MUC1 is associated with acquisition of characteristic properties of cancer cells (proliferation, migration, invasion, metastasis) and tumor progression. This project aims to decipher the mechanisms by which MUC1 induces epithelial renal carcinogenesis and chemoresistance. We then consider to make MUC1 a new therapeutic target and thus develop new potential molecules, in order to widen the panel of available therapies.</dcterms:abstract>
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