Undecylprodigiosin Induced Apoptosis in P388 Cancer Cells Is Associated with Its Binding to Ribosome
Liu, Ping1,2; Wang, Yuan-yuan1; Qi, Xin1; Gu, QianQun1; Geng, Meiyu3; Li, Jing1
发表期刊PLOS ONE
ISSN1932-6203
2013-06-14
卷号8期号:6页码:e65381
关键词Cycloprodigiosin Hydrochloride h+/cl-symporter Hl-60 Cells h+-atpase In-vitro Prodigiosin Lines Differentiation Proliferation Inhibition
产权排序[Liu, Ping; Wang, Yuan-yuan; Qi, Xin; Gu, QianQun; Li, Jing] Ocean Univ China, Sch Med & Pharm, Minist Educ, Key Lab Marine Drugs, Qingdao, Peoples R China; [Liu, Ping] Chinese Acad Sci, Anal & Testing Ctr, Yantai Inst Coastal Zone Res, Yantai, Peoples R China; [Geng, Meiyu] Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Drug Res, Shanghai 200031, Peoples R China
通讯作者Geng, MY (reprint author), Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Drug Res, Shanghai 200031, Peoples R China. mygeng@mail.shcnc.ac.cn ; lijing_ouc@ouc.edu.cn
作者部门海岸带生物学与生物资源利用所重点实验室
英文摘要Prodigiosins (PGs) are a family of natural red pigments with anticancer activity, and one member of the family has entered clinical phase II trials. However, the anticancer mechanisms of PGs remain largely unclear. This study was designed to investigate the molecular basis of anticancer activity of UP, a derivative of PGs, in P388 cells. By introducing pharmacological inhibitors and utilizing a variety of analytical approaches including western blotting, flow cytometry and confocal laser microscopy, we found that UP inhibited proliferation of P388 via arresting cells at G2/M phase and inducing cells apoptosis, which was related to the activation of P38, JNK rather than ERK1/2 signaling. ROS regeneration and acidification in cells appear not involved in UP induced apoptosis. Furthermore, utilizing mass spectrometry, sucrose density gradient fractionation and immunofluorescence staining, we discovered that UP was apparently located at ribosome. These results together indicate that ribosome may be the potential target of UP in cancer cells, which opened a new avenue in delineating the anticancer mechanism of PGs.; Prodigiosins (PGs) are a family of natural red pigments with anticancer activity, and one member of the family has entered clinical phase II trials. However, the anticancer mechanisms of PGs remain largely unclear. This study was designed to investigate the molecular basis of anticancer activity of UP, a derivative of PGs, in P388 cells. By introducing pharmacological inhibitors and utilizing a variety of analytical approaches including western blotting, flow cytometry and confocal laser microscopy, we found that UP inhibited proliferation of P388 via arresting cells at G2/M phase and inducing cells apoptosis, which was related to the activation of P38, JNK rather than ERK1/2 signaling. ROS regeneration and acidification in cells appear not involved in UP induced apoptosis. Furthermore, utilizing mass spectrometry, sucrose density gradient fractionation and immunofluorescence staining, we discovered that UP was apparently located at ribosome. These results together indicate that ribosome may be the potential target of UP in cancer cells, which opened a new avenue in delineating the anticancer mechanism of PGs.
文章类型Article
资助机构National High-tech R&D Program of China [2011AA09070104]; Program for Changjiang Scholars and Innovative Research Team in University [IRT0944]
收录类别SCI
语种英语
关键词[WOS]CYCLOPRODIGIOSIN HYDROCHLORIDE ; H+/CL-SYMPORTER ; HL-60 CELLS ; H+-ATPASE ; IN-VITRO ; PRODIGIOSIN ; LINES ; DIFFERENTIATION ; PROLIFERATION ; INHIBITION
研究领域[WOS]Science & Technology - Other Topics
WOS记录号WOS:000320363300018
引用统计
被引频次:18[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.yic.ac.cn/handle/133337/6474
专题海岸带生物学与生物资源利用重点实验室_海岸带生物学与生物资源保护实验室
作者单位1.Ocean Univ China, Sch Med & Pharm, Minist Educ, Key Lab Marine Drugs, Qingdao, Peoples R China
2.Chinese Acad Sci, Anal & Testing Ctr, Yantai Inst Coastal Zone Res, Yantai, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Drug Res, Shanghai 200031, Peoples R China
推荐引用方式
GB/T 7714
Liu, Ping,Wang, Yuan-yuan,Qi, Xin,et al. Undecylprodigiosin Induced Apoptosis in P388 Cancer Cells Is Associated with Its Binding to Ribosome[J]. PLOS ONE,2013,8(6):e65381.
APA Liu, Ping,Wang, Yuan-yuan,Qi, Xin,Gu, QianQun,Geng, Meiyu,&Li, Jing.(2013).Undecylprodigiosin Induced Apoptosis in P388 Cancer Cells Is Associated with Its Binding to Ribosome.PLOS ONE,8(6),e65381.
MLA Liu, Ping,et al."Undecylprodigiosin Induced Apoptosis in P388 Cancer Cells Is Associated with Its Binding to Ribosome".PLOS ONE 8.6(2013):e65381.
条目包含的文件
文件名称/大小 文献类型 版本类型 开放类型 使用许可
Undecylprodigiosin I(2380KB) 开放获取--浏览 请求全文
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Liu, Ping]的文章
[Wang, Yuan-yuan]的文章
[Qi, Xin]的文章
百度学术
百度学术中相似的文章
[Liu, Ping]的文章
[Wang, Yuan-yuan]的文章
[Qi, Xin]的文章
必应学术
必应学术中相似的文章
[Liu, Ping]的文章
[Wang, Yuan-yuan]的文章
[Qi, Xin]的文章
相关权益政策
暂无数据
收藏/分享
文件名: Undecylprodigiosin Induced Apoptosis in P388 Cancer Cells Is Associated with Its Binding to Ribosome.pdf
格式: Adobe PDF
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。