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乳腺癌转移中的磷脂酰胆碱和溶血磷脂酰胆碱分析
引用本文:尤嘉琮,杨杰,方润平,胡楠,张晓东,张伟英,叶丽虹.乳腺癌转移中的磷脂酰胆碱和溶血磷脂酰胆碱分析[J].生物化学与生物物理进展,2015,42(6):563-573.
作者姓名:尤嘉琮  杨杰  方润平  胡楠  张晓东  张伟英  叶丽虹
作者单位:南开大学生命科学学院生物化学与分子生物学系蛋白质生化研究室,药物化学生物学国家重点实验室,天津 300071,天津大学化工学院,天津 300072,南开大学生命科学学院生物化学与分子生物学系蛋白质生化研究室,药物化学生物学国家重点实验室,天津 300071,南开大学生命科学学院生物化学与分子生物学系蛋白质生化研究室,药物化学生物学国家重点实验室,天津 300071,南开大学生命科学学院生物化学与分子生物学系肿瘤研究室,药物化学生物学国家重点实验室,天津 300071,南开大学生命科学学院生物化学与分子生物学系蛋白质生化研究室,药物化学生物学国家重点实验室,天津 300071,南开大学生命科学学院生物化学与分子生物学系蛋白质生化研究室,药物化学生物学国家重点实验室,天津 300071
基金项目:天津市自然科学基金(14JCZDJC32800),国家重点基础研究发展计划(973)(2015CB553905),国家高技术研究发展计划(863)(2014AA020903)和国家自然科学基金(81372186)资助项目
摘    要:我们以前曾报道花生四烯酸(arachidonic acid,AA)代谢产物可以促进乳腺癌细胞增殖和迁移。为了进一步寻找维持高转移乳腺癌细胞中AA高水平代谢的内源机制,深入探求AA代谢促进乳腺癌细胞转移的分子机理,我们应用HPLC/ESI/MSn技术检测和分析了乳腺癌MCF-7和高转移乳腺癌LM-MCF-7细胞中溶血磷脂酰胆碱(lysophosphatidylcholines,LysoPCs)和磷脂酰胆碱(phosphatidylcholines,PCs)的成分和含量。我们发现了10种LysoPC的含量在LM-MCF-7细胞中显著高于MCF-7细胞,有6种PC可水解产生AA,它们在LM-MCF-7细胞中的含量显著低于MCF-7细胞,提示这些溶血磷脂含量的升高和磷脂含量的降低可能与乳腺癌转移相关。在LM-MCF-7细胞中,COX-2抑制剂吲哚美辛(indomethacin,Indo)和LOX抑制剂(nordihydroguaiaretic acid,NDGA)共同作用可明显下调cPLA2的活性,应用HPLC-ESI-MSn技术比较cPLA2活性下调前后LM-MCF-7细胞中LysoPC和PC含量的变化,发现其中4种PC可被cPLA2水解产生AA。我们还发现,细胞内LysoPC与PC的比值可以反映cPLA2的活性。通过以上研究我们进一步证实了由cPLA2活性调节的AA释放及代谢对乳腺癌转移具有重要作用。

关 键 词:磷脂酰胆碱,溶血磷脂酰胆碱,cPLA2,乳腺癌
收稿时间:2015/1/27 0:00:00
修稿时间:2015/4/29 0:00:00

Analysis of Phosphatidylcholines (PCs) and Lysophosphatidylcholines (LysoPCs) in Metastasis of Breast Cancer Cells
YOU Jia-Cong,YANG Jie,FANG Run-Ping,HU Nan,ZHANG Xiao-Dong,ZHANG Wei-Ying and YE Li-Hong.Analysis of Phosphatidylcholines (PCs) and Lysophosphatidylcholines (LysoPCs) in Metastasis of Breast Cancer Cells[J].Progress In Biochemistry and Biophysics,2015,42(6):563-573.
Authors:YOU Jia-Cong  YANG Jie  FANG Run-Ping  HU Nan  ZHANG Xiao-Dong  ZHANG Wei-Ying and YE Li-Hong
Institution:State Key Laboratory of Medicinal Chemical Biology, Department of Biochemistry, College of Life Sciences,Nankai University, Tianjin 300071, China,Department of Pharmaceutical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China,State Key Laboratory of Medicinal Chemical Biology, Department of Biochemistry, College of Life Sciences,Nankai University, Tianjin 300071, China,State Key Laboratory of Medicinal Chemical Biology, Department of Biochemistry, College of Life Sciences,Nankai University, Tianjin 300071, China,State Key Laboratory of Medicinal Chemical Biology, Department of Cancer Research, College of Life Sciences,Nankai University, Tianjin 300071, China,State Key Laboratory of Medicinal Chemical Biology, Department of Biochemistry, College of Life Sciences,Nankai University, Tianjin 300071, China and State Key Laboratory of Medicinal Chemical Biology, Department of Biochemistry, College of Life Sciences,Nankai University, Tianjin 300071, China
Abstract:The important role of phospholipids in many processes including cell cycle regulation, inflammation and tumorigenesis is increasingly becoming the focus of research. Previously we found that cytosolic phospholipase A2 (cPLA2) is over-expressed in breast cancer cells. Here, we assessed the profiles of phosphatidylcholines (PCs) and lysophosphatidylcholines (LysoPCs) that were mediated by cPLA2 in breast cancer cells. MCF-7 and LM-MCF-7 (with high metastatic potential) cell lines were used as models and the profiles of phospholipids were analyzed by HPLC/ESI/MSn. Our results showed that the levels of 10 species of LysoPCs were higher in LM-MCF-7 cells than that in MCF-7 cells. Meanwhile, six species of PCs that may produce arachidonic acid (AA) and associated LysoPCs were lower in LM-MCF-7 cells than that in MCF-7 cells. Furthermore, we identified that 4 out of 6 species of PCs were responsible for the generation of AA mediated by cPLA2 in LM-MCF-7 cells. The increased ratio of LysoPCs to PCs corresponds to the activation level of cPLA2. Thus, we conclude that 4 identified species of PCs and 4 corresponding species of LysoPCs mediated by cPLA2, as well as the up-regulation and activation of cPLA2, may involve in the metastasis of breast cancer cells.
Keywords:phosphatidylcholine (PC)  lysophosphatidylcholine (LysoPC)  cytosolic phospholipase A2 (cPLA2)  breast cancer
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