题名 | W346 inhibits cell growth, invasion, induces cycle arrest and potentiates apoptosis in human gastric cancer cells in vitro through the NF-kappa B signaling pathway |
作者 | |
发表日期 | 2016-04 |
发表期刊 | TUMOR BIOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | W346 Anticancer drug Curcumin Gastric cancer Apoptosis NF-kappa B |
其他关键词 | MONO-CARBONYL ANALOGS ; CURCUMIN SUPPRESSES PROLIFERATION ; REGULATED GENE-PRODUCTS ; TUMOR-GROWTH ; PANCREATIC-CANCER ; DOWN-REGULATION ; ACTIVATION ; ANGIOGENESIS ; MODULATION ; EXPRESSION |
摘要 | The therapeutic agent selectively killing cancer cells is urgently needed for gastric cancer treatment. Curcumin has been investigated for its effect on the cancer treatment because of its significant therapeutic potential and safety profile. A synthetic unsymmetry mono-carbonyl compound termed W346 was developed from curcumin. In this study, we investigated the potential antineoplastic effect and mechanism of W346 against human gastric cancer cells. W346 suppressed the proliferation and invasion, blocked cell cycle arrest at G2/M phase, and increased apoptosis in gastric cancer cells, and it presented obviously improved anticancer activity than curcumin. Moreover, W346 effectively inhibited tumor necrosis factor (TNF-alpha)-induced NF-kappa B activation by suppressing IKK phosphorylation, inhibiting I kappa B-alpha degradation, and restraining the accumulation of NF-kappa B subunit p65 nuclear translocation. W346 also affected NF-kappa B-regulated downstream products involved in cycle arrest and apoptosis. In a word, W346 exhibited significantly improved anti-gastric cancer activity over curcumin by targeting NF-kappa B signaling pathway, and it is likely to be a promising starting point for the development of curcumin-based therapeutic agent. |
资助项目 | National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81272462]; Zhejiang Province Natural Science Fund of China [LY14H160044, Y13H300005]; Technology Foundation for Medical Science of Zhejiang Province [2012KYA129] |
出版者 | SPRINGER |
出版地 | DORDRECHT |
ISSN | 1010-4283 |
EISSN | 1423-0380 |
卷号 | 37期号:4页码:4791-4801 |
DOI | 10.1007/s13277-015-4277-2 |
页数 | 11 |
WOS类目 | Oncology |
WOS研究方向 | Oncology |
WOS记录号 | WOS:000374904500061 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 26520440 |
SCOPUSEID | 2-s2.0-84945569562 |
通讯作者地址 | [Jin, Rong]Chemical Biology Research Center,College of Pharmaceutical Sciences,Wenzhou Medical University,Wenzhou,325035,China |
Scopus学科分类 | Cancer Research |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/5229 |
专题 | 附属第一医院 温州医科大学 药学院(分析测试中心)_药学系 |
通讯作者 | Jin, Rong |
作者单位 | 1.Department of Digestive Diseases,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325000,China; 2.Chemical Biology Research Center,College of Pharmaceutical Sciences,Wenzhou Medical University,Wenzhou,325035,China; 3.Pharmacy Department,Tonglu First People’s Hospital,Hangzhou,311500,China; 4.Institute of Sports Science,Wenzhou Medical University,Wenzhou,325035,China; 5.Department of General Surgery,The fifth Affiliated Hospital of Guangzhou Medical University,Guangzhou,510700,China |
第一作者单位 | 附属第一医院; 药学院(分析测试中心)_药学系 |
通讯作者单位 | 药学院(分析测试中心)_生物有机与药物化学研究中心 |
第一作者的第一单位 | 附属第一医院 |
推荐引用方式 GB/T 7714 | Xia, Yiqun,Weng, Bixia,Wang, Zhankun,et al. W346 inhibits cell growth, invasion, induces cycle arrest and potentiates apoptosis in human gastric cancer cells in vitro through the NF-kappa B signaling pathway[J]. TUMOR BIOLOGY,2016,37(4):4791-4801. |
APA | Xia, Yiqun., Weng, Bixia., Wang, Zhankun., Kang, Yanting., Shi, Lingyi., ... & Liang, Guang. (2016). W346 inhibits cell growth, invasion, induces cycle arrest and potentiates apoptosis in human gastric cancer cells in vitro through the NF-kappa B signaling pathway. TUMOR BIOLOGY, 37(4), 4791-4801. |
MLA | Xia, Yiqun,et al."W346 inhibits cell growth, invasion, induces cycle arrest and potentiates apoptosis in human gastric cancer cells in vitro through the NF-kappa B signaling pathway".TUMOR BIOLOGY 37.4(2016):4791-4801. |
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