High levels of sphingolipids in human breast cancer.
High levels of sphingolipids in human breast cancer.
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DOI:
10.1016/j.jss.2016.05.022
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发表时间:
2016-08
影响因子:
2.2
通讯作者:
Wakai, Toshifumi
中科院分区:
文献类型:
--
作者:
Nagahashi, Masayuki;Tsuchida, Junko;Moro, Kazuki;Hasegawa, Miki;Tatsuda, Kumiko;Woelfel, Ingrid A.;Takabe, Kazuaki;Wakai, Toshifumi
Sphingolipids, including sphingosine-1-phosphate (S1P) and ceramide, have emerged as key regulatory molecules that control various aspects of cell growth and proliferation in cancer. Although important roles of sphingolipids in breast cancer progression have been reported in experimental models, their roles in human patients have yet to be determined. The aim of this study is to determine the levels of sphingolipids including S1P, ceramides, and other sphingolipids, in breast cancer and normal breast tissue and to compare the difference in levels of each sphingolipid between the two tissues. Tumor and non-cancerous breast tissue were obtained from 12 patients with breast cancer. Sphingolipids including S1P, ceramides, and their metabolites of sphingosine, sphingomyelin, and monohexosylceramide were measured by liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS). The levels of S1P, ceramides, and other sphingolipids in the tumor were significantly higher than those in normal breast tissue. There was a relatively strong correlation in the levels of S1P between the tumor and that of normal breast tissue from the same person. On the other hand, there was no correlation in the levels of most of the ceramide species between the tumor and that of normal breast tissue from the same person. To our knowledge this is the first study to reveal that levels of sphingolipids in cancer tissue are generally higher than normal breast tissue in patients with breast cancer. The correlation of S1P levels in these tissues implicates the role of S1P in interaction between cancer and the tumor microenvironment.
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DOI:
10.4137/bcbcr.s25460
发表时间:
2015
期刊:
Breast cancer : basic and clinical research
影响因子:
--
作者:
Jin X;Mu P
通讯作者:
Mu P
DOI:
10.1126/science.1176709
发表时间:
2009-09-04
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Hait NC;Allegood J;Maceyka M;Strub GM;Harikumar KB;Singh SK;Luo C;Marmorstein R;Kordula T;Milstien S;Spiegel S
通讯作者:
Spiegel S
影响因子:
2.7
作者:
Knapp, M.;Baranowski, M.;Musial, W.
通讯作者:
Musial, W.
影响因子:
11.2
作者:
Nagahashi M;Ramachandran S;Kim EY;Allegood JC;Rashid OM;Yamada A;Zhao R;Milstien S;Zhou H;Spiegel S;Takabe K
通讯作者:
Takabe K
影响因子:
4.7
作者:
Pyne S;Edwards J;Ohotski J;Pyne NJ
通讯作者:
Pyne NJ