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AGENTS TARGETING SNAT7 FOR TREATING CELLULAR METABOLISM REPROGRAMMING-ASSOCIATED DISEASES

机译:代理商针对SNAT7来治疗细胞代谢重编程相关疾病

摘要

The present application relates to therapeutic agent reducing the expression or the activity of the SNAT7 transporter, encoded by the SLC38A7 gene or one of its variants for use in the treatment of a cellular metabolism reprogramming-associated disease, preferentially a cancer depending on glutamine, more preferentially a cancer depending on glutamine activated by one or more oncogenes selected from Ras, Myc and Src, even more preferentially a cancer depending on glutamine activated by Ras. The present invention also relates to a pharmaceutical composition comprising at least one therapeutic agent for use according to the invention, or at least one expression vector according expressing said therapeutic agent for use to the invention.
机译:本申请涉及降低由 SLC38A7 基因或其变体之一编码的SNAT7转运蛋白的表达或活性的治疗剂,优选用于治疗与细胞代谢重编程相关的疾病取决于谷氨酰胺的癌症,更优选取决于由一种或多种选自Ras,Myc和Src的癌基因激活的谷氨酰胺的癌症,甚至更优选取决于由Ras激活的谷氨酰胺的癌症。本发明还涉及药物组合物,其包含至少一种根据本发明使用的治疗剂,或至少一种根据表达所述用于本发明的治疗剂的表达载体。

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