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LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma

Tumor cells require high levels of cholesterol for membrane biogenesis for rapid proliferation during development. Beyond the acquired cholesterol from low-density lipoprotein (LDL) taken up from circulation, tumor cells can also biosynthesize cholesterol. The molecular mechanism underlying choleste...

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Autores principales: Tao, Mingyue, Luo, Jing, Gu, Tong, Yu, Xiaojuan, Song, Zhen, Jun, Yali, Gu, Hao, Han, Kairong, Huang, Xiujuan, Yu, Weiyong, Sun, Su’an, Zhang, Zhengwei, Liu, Lu, Chen, Xiaofei, Zhang, Li, Luo, Chao, Wang, Qilong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438019/
https://www.ncbi.nlm.nih.gov/pubmed/34518524
http://dx.doi.org/10.1038/s41419-021-04132-6
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author Tao, Mingyue
Luo, Jing
Gu, Tong
Yu, Xiaojuan
Song, Zhen
Jun, Yali
Gu, Hao
Han, Kairong
Huang, Xiujuan
Yu, Weiyong
Sun, Su’an
Zhang, Zhengwei
Liu, Lu
Chen, Xiaofei
Zhang, Li
Luo, Chao
Wang, Qilong
author_facet Tao, Mingyue
Luo, Jing
Gu, Tong
Yu, Xiaojuan
Song, Zhen
Jun, Yali
Gu, Hao
Han, Kairong
Huang, Xiujuan
Yu, Weiyong
Sun, Su’an
Zhang, Zhengwei
Liu, Lu
Chen, Xiaofei
Zhang, Li
Luo, Chao
Wang, Qilong
author_sort Tao, Mingyue
collection PubMed
description Tumor cells require high levels of cholesterol for membrane biogenesis for rapid proliferation during development. Beyond the acquired cholesterol from low-density lipoprotein (LDL) taken up from circulation, tumor cells can also biosynthesize cholesterol. The molecular mechanism underlying cholesterol anabolism in esophageal squamous cell carcinoma (ESCC) and its effect on patient prognosis are unclear. Dysregulation of lipid metabolism is common in cancer. Lysophosphatidylcholine acyltransferase 1 (LPCAT1) has been implicated in various cancer types; however, its role in esophageal squamous cell carcinoma (ESCC) remains unclear. In this study, we identified that LPCAT1 is highly expressed in ESCC and that LPCAT1 reprograms cholesterol metabolism in ESCC. LPCAT1 expression was negatively correlated with patient prognosis. Cholesterol synthesis in ESCC cells was significantly inhibited following LPCAT1 knockdown; cell proliferation, invasion, and migration were significantly reduced, along with the growth of xenograft subcutaneous tumors. LPCAT1 could regulate the expression of the cholesterol synthesis enzyme, SQLE, by promoting the activation of PI3K, thereby regulating the entry of SP1/SREBPF2 into the nucleus. LPCAT1 also activates EGFR leading to the downregulation of INSIG-1 expression, facilitating the entry of SREBP-1 into the nucleus to promote cholesterol synthesis. Taken together, LPCAT1 reprograms tumor cell cholesterol metabolism in ESCC and can be used as a potential treatment target against ESCC.
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spelling pubmed-84380192021-09-24 LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma Tao, Mingyue Luo, Jing Gu, Tong Yu, Xiaojuan Song, Zhen Jun, Yali Gu, Hao Han, Kairong Huang, Xiujuan Yu, Weiyong Sun, Su’an Zhang, Zhengwei Liu, Lu Chen, Xiaofei Zhang, Li Luo, Chao Wang, Qilong Cell Death Dis Article Tumor cells require high levels of cholesterol for membrane biogenesis for rapid proliferation during development. Beyond the acquired cholesterol from low-density lipoprotein (LDL) taken up from circulation, tumor cells can also biosynthesize cholesterol. The molecular mechanism underlying cholesterol anabolism in esophageal squamous cell carcinoma (ESCC) and its effect on patient prognosis are unclear. Dysregulation of lipid metabolism is common in cancer. Lysophosphatidylcholine acyltransferase 1 (LPCAT1) has been implicated in various cancer types; however, its role in esophageal squamous cell carcinoma (ESCC) remains unclear. In this study, we identified that LPCAT1 is highly expressed in ESCC and that LPCAT1 reprograms cholesterol metabolism in ESCC. LPCAT1 expression was negatively correlated with patient prognosis. Cholesterol synthesis in ESCC cells was significantly inhibited following LPCAT1 knockdown; cell proliferation, invasion, and migration were significantly reduced, along with the growth of xenograft subcutaneous tumors. LPCAT1 could regulate the expression of the cholesterol synthesis enzyme, SQLE, by promoting the activation of PI3K, thereby regulating the entry of SP1/SREBPF2 into the nucleus. LPCAT1 also activates EGFR leading to the downregulation of INSIG-1 expression, facilitating the entry of SREBP-1 into the nucleus to promote cholesterol synthesis. Taken together, LPCAT1 reprograms tumor cell cholesterol metabolism in ESCC and can be used as a potential treatment target against ESCC. Nature Publishing Group UK 2021-09-13 /pmc/articles/PMC8438019/ /pubmed/34518524 http://dx.doi.org/10.1038/s41419-021-04132-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tao, Mingyue
Luo, Jing
Gu, Tong
Yu, Xiaojuan
Song, Zhen
Jun, Yali
Gu, Hao
Han, Kairong
Huang, Xiujuan
Yu, Weiyong
Sun, Su’an
Zhang, Zhengwei
Liu, Lu
Chen, Xiaofei
Zhang, Li
Luo, Chao
Wang, Qilong
LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma
title LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma
title_full LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma
title_fullStr LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma
title_full_unstemmed LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma
title_short LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma
title_sort lpcat1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438019/
https://www.ncbi.nlm.nih.gov/pubmed/34518524
http://dx.doi.org/10.1038/s41419-021-04132-6
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