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