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用紫杉醇和 muramyl dipeptide 衍生物缀合物拮抗 NOD2 信号转导可增强紫杉醇治疗效果并显著预防肿瘤转移。

Antagonizing NOD2 Signaling with Conjugates of Paclitaxel and Muramyl Dipeptide Derivatives Sensitizes Paclitaxel Therapy and Significantly Prevents Tumor Metastasis.

机构信息

School of Pharmaceutical Sciences, Tsinghua University , Haidian District, Beijing 100084, P. R. China.

Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College , 2A Nanwei Road, Xicheng District, Beijing 100050, P. R. China.

出版信息

J Med Chem. 2017 Feb 9;60(3):1219-1224. doi: 10.1021/acs.jmedchem.6b01704. Epub 2017 Jan 24.

Abstract

A noncleavable paclitaxel (PTX) and N-acetylmuramyl-l-alanyl-d-isoglutamine (MDP) derivative conjugate, 22 (DY-16-43), and its analogues were prepared and characterized as antagonists of NOD2 signaling. This conjugate enhanced the antitumor and antimetastatic efficacy of PTX in Lewis lung carcinoma (LLC) tumor-bearing mice. This work first describes a molecular strategy that enables the sensitization of a chemotherapeutic response via antagonizing NOD2 inflammatory signaling and suggests NOD2 antagonist as potential adjunct in treating non-small-cell lung cancer (NSCLC).

摘要

一种不可裂解的紫杉醇(PTX)和 N-乙酰基胞壁酰-L-丙氨酰-D-异谷氨酰胺(MDP)衍生物缀合物 22(DY-16-43)及其类似物被制备并表征为 NOD2 信号的拮抗剂。该缀合物增强了紫杉醇在 Lewis 肺癌(LLC)荷瘤小鼠中的抗肿瘤和抗转移疗效。这项工作首次描述了一种分子策略,通过拮抗 NOD2 炎症信号来增强化疗反应的敏感性,并表明 NOD2 拮抗剂可能是治疗非小细胞肺癌(NSCLC)的潜在辅助手段。

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