Parthenolide from Parthenium integrifolium reduces tumor burden and alleviate cachexia symptoms in the murine CT-26 model of colorectal carcinoma

被引:21
作者
Yang Quanjun [1 ,2 ]
Wan Lili [1 ]
Zhou Zhiyong [1 ,2 ]
Li Yan [1 ]
Yu Qi [1 ]
Liu Liya [1 ,3 ]
Li Bin [1 ,3 ]
Guo Cheng [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 6, Dept Pharm, Shanghai 200233, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200240, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Shanghai 201203, Peoples R China
关键词
Cancer cachexia; Parthenolide; Parthenium integrifolium; Tumor burden; Skeletal muscle; NF-KAPPA-B; SESQUITERPENE LACTONE PARTHENOLIDE; EXPERIMENTAL CANCER CACHEXIA; IN-VIVO; ANTIINFLAMMATORY ACTIVITY; SEPSIS; KINASE; CELLS; INVOLVEMENT; METASTASIS;
D O I
10.1016/j.phymed.2013.04.020
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Excessive elaboration of proinflammatory cytokines are involved in cachexia-related hypercatabolism. Parthenolide, as a potential anti-inflammatory active agent, could effectively inhibit nuclear factor-kappa B, and has the potential for the treatment of cancer cachexia. In this study, the cancer cachexia model was established by subcutaneous transplantation CT26 tumor fragment. Parthenolide or placebo was intraperitoneally given daily from the next day. Parthenolide treatment could effectively preserve the body weight, improve the mass of gastrocnemius and tibialis anterior muscles, and alleviate tumor burden. Sizes of muscle fibers and myosin heavy chain were also increasing. The serum proinflammatory cytokine TNF-alpha level was lower than placebo treatment mice measure by ELISA. To investigate the possible mechanism, MuRF1 and Fbx32 was subjected to Western blot analysis and expression of MURF1 was inhibited in gastrocnemius muscle. Collectively, parthenolide treatment could effectively alleviate tumor burden of cachexia, preserve the body weight and improve skeletal muscle characteristics. (C) 2013 Elsevier GmbH. All rights reserved.
引用
收藏
页码:992 / 998
页数:7
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