4.5 Article

Lipidomic profiling reveals lipid regulation by a novel LSD1 inhibitor treatment

期刊

ONCOLOGY REPORTS
卷 46, 期 5, 页码 -

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/or.2021.8184

关键词

LSD1; LSD1 inhibitor; lipidomics; sphingolipids; ceramide

类别

资金

  1. National Natural Sciences Foundation of China [81773198]
  2. National Keypoint Research and Invention Program of the China Ministry of Science and Technology [MOST-2016YFC1303200]
  3. National ST Major project [2018ZX09201018]
  4. Science and Technology Innovation Program of Shanxi Provincial Education Department [2020L0177]
  5. Funding for Doctoral Research of Shanxi Province [3C322019039]

向作者/读者索取更多资源

The study demonstrates that LSD1 inhibitor ZY0511 significantly alters lipid metabolism in colorectal and cervical cancer cells, reducing levels of phosphatidylserine, phosphatidylethanolamine, phosphatidylcholine, and sphingomyelin. This suggests that LSD1 may regulate cancer progression by affecting lipid metabolism.
Lipid metabolic alterations are associated with cancer progression. Lysine-specific demethylase 1 (LSD1) plays a crucial role in cancer and has become a promising target for cancer therapy. However, the effect of LSD1 on lipid metabolism remains unclear. In the present study, we used a LC-MS/MS-based lipidomics approach to investigate the impact of LSD1 on cancer cell lipid metabolism using ZY0511, a specific LSD1 inhibitor developed by our group as a specific probe. ZY0511 profoundly modified the human colorectal and cervical cancer cell lipid metabolism. A total of 256 differential metabolites were identified in HeLa cells, and 218 differential metabolites were identified in HCT116 cells, respectively. Among these lipid metabolites, phosphatidylserine, phosphatidylethanolamine, phosphatidylcholine and sphingomyelin (SM) were downregulated by ZY0511. In contrast, ceramide (Cer) and a small portion of glycerophospholipids such as phosphatidylinositol and phosphatidylethanolamine were upregulated by ZY0511. These results revealed a disturbance in sphingolipids (SPs) and glycerophospholipids, which may be correlated with the progression of cancer. Furthermore, a marked increase in Cer and prominent decrease in SM were consistent with the upregulated expression of key enzymes in the Cer synthesis process including de novo synthesis, hydrolysis of SM and the salvage pathway after ZY0511 exposure. In conclusion, our research reveals a link between LSD1 and lipid metabolism in cancer cells, offering more comprehensive evidence for the application of LSD1 inhibitors for cancer therapy. The underlying mechanisms of how the LSD1 inhibitor regulates lipid metabolism warrant further investigation.

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