Journal article
MiR-210: A potential therapeutic target against radiation-induced enteropathy.
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Hamama S
INSERM U-1030 "Molecular Radiotherapy", Institut Gustave Roussy, Villejuif, France; LabEX LERMIT Villejuif, France; Université Paris Sud Paris XI, Le Kremlin Bicêtre, France. Electronic address: saad.hamama@igr.fr.
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Noman MZ
INSERM, U753, Laboratoire d'immunologie des Tumeurs Humaines: Interaction Effecteurs Cytotoxiques-Système Tumoral, Institut Gustave-Roussy, Villejuif, France. Electronic address: muhammed-zaeem.noman@igr.fr.
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Gervaz P
Geneva University Hospital and Medical School, Geneva, Switzerland. Electronic address: pascal.gervaz@lacolline.ch.
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Delanian S
Unité de Radiopathologie, Service Oncologie-Radiothérapie, Hôpital Saint-Louis, APHP, Paris, France. Electronic address: sylvie.delanian@sls.aphp.fr.
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Vozenin MC
INSERM U-1030 "Molecular Radiotherapy", Institut Gustave Roussy, Villejuif, France; LabEX LERMIT Villejuif, France; Université Paris Sud Paris XI, Le Kremlin Bicêtre, France; Laboratoire de RadioOncologie, Swiss Cancer Center of Lausanne, CHUV, Lausanne, Switzerland. Electronic address: marie-catherine.vozenin@chuv.ch.
Published in:
- Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology. - 2014
English
A previously undescribed and robust miR210 overexpression is shown in intestinal samples obtained from patients with radiation enteropathy and fibrotic cultured cells. In addition, miR-210 overexpression is repressed by antifibrotic treatment combining pentoxifylline and α-tocopherol.
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Language
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Open access status
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closed
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Identifiers
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Persistent URL
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https://sonar.ch/global/documents/108698
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