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Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells

BACKGROUND: Anlotinib has demonstrated encouraging clinical outcomes in the treatment of lung cancer, soft tissue sarcoma and thyroid carcinoma. Several clinical studies have shown a relationship between anlotinib treatment and the occurrence of hyperlipidemia. The fundamental mechanisms, however, a...

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Autores principales: Zhu, Zhongling, Xu, Shan, Ren, Jing, Jiang, Teng, Zhang, Cai, Yan, Zhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464365/
https://www.ncbi.nlm.nih.gov/pubmed/37612751
http://dx.doi.org/10.1186/s12944-023-01907-y
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author Zhu, Zhongling
Xu, Shan
Ren, Jing
Jiang, Teng
Zhang, Cai
Yan, Zhao
author_facet Zhu, Zhongling
Xu, Shan
Ren, Jing
Jiang, Teng
Zhang, Cai
Yan, Zhao
author_sort Zhu, Zhongling
collection PubMed
description BACKGROUND: Anlotinib has demonstrated encouraging clinical outcomes in the treatment of lung cancer, soft tissue sarcoma and thyroid carcinoma. Several clinical studies have shown a relationship between anlotinib treatment and the occurrence of hyperlipidemia. The fundamental mechanisms, however, are still largely unclear. Here, the effect of anlotinib on lipid metabolism in an animal model and human cancer cells was evaluated and the role of lipid metabolism in the antitumor efficacy of anlotinib was investigated. METHODS: The C57BL/6 J mouse model as well as A549 and H460 human lung cancer cell lines were used to examine the impact of anlotinib on lipid metabolism both in vivo and in vitro. Levels of triglycerides, high-density lipoprotein, low-density lipoprotein (LDL), and total cholesterol in serum or cell samples were determined using assay kits. The expression levels of crucial genes and proteins involved in lipid metabolism were measured by quantitative RT-PCR and Western blotting. Furthermore, exogenous LDL and knockdown of low-density lipoprotein receptor (LDLR) were used in H460 cells to investigate the relevance of lipid metabolism in the anticancer efficacy of anlotinib. RESULTS: Anlotinib caused hyperlipidemia in C57BL/6 J mice, possibly by downregulating hepatic LDLR-mediated uptake of LDL cholesterol. AMP-activated protein kinase and mammalian target of rapamycin inhibition may also be involved. Additionally, anlotinib enhanced sterol response element binding protein 1/2 nuclear accumulation as well as upregulated LDLR expression in A549 and H460 cells, which may be attributable to intracellular lipid accumulation. Knockdown of LDLR reduced intracellular cholesterol content, but interestingly, anlotinib significantly improved intracellular cholesterol accumulation in LDLR-knockdown cells. Both exogenous LDL and LDLR knockdown decreased the sensitivity of cells to anlotinib. CONCLUSIONS: Anlotinib modulates host lipid metabolism through multiple pathways. Anlotinib also exerts a significant impact on lipid metabolism in cancer cells by regulating key transcription factors and metabolic enzymes. In addition, these findings suggest lipid metabolism is implicated in anlotinib sensitivity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-023-01907-y.
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spelling pubmed-104643652023-08-30 Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells Zhu, Zhongling Xu, Shan Ren, Jing Jiang, Teng Zhang, Cai Yan, Zhao Lipids Health Dis Research BACKGROUND: Anlotinib has demonstrated encouraging clinical outcomes in the treatment of lung cancer, soft tissue sarcoma and thyroid carcinoma. Several clinical studies have shown a relationship between anlotinib treatment and the occurrence of hyperlipidemia. The fundamental mechanisms, however, are still largely unclear. Here, the effect of anlotinib on lipid metabolism in an animal model and human cancer cells was evaluated and the role of lipid metabolism in the antitumor efficacy of anlotinib was investigated. METHODS: The C57BL/6 J mouse model as well as A549 and H460 human lung cancer cell lines were used to examine the impact of anlotinib on lipid metabolism both in vivo and in vitro. Levels of triglycerides, high-density lipoprotein, low-density lipoprotein (LDL), and total cholesterol in serum or cell samples were determined using assay kits. The expression levels of crucial genes and proteins involved in lipid metabolism were measured by quantitative RT-PCR and Western blotting. Furthermore, exogenous LDL and knockdown of low-density lipoprotein receptor (LDLR) were used in H460 cells to investigate the relevance of lipid metabolism in the anticancer efficacy of anlotinib. RESULTS: Anlotinib caused hyperlipidemia in C57BL/6 J mice, possibly by downregulating hepatic LDLR-mediated uptake of LDL cholesterol. AMP-activated protein kinase and mammalian target of rapamycin inhibition may also be involved. Additionally, anlotinib enhanced sterol response element binding protein 1/2 nuclear accumulation as well as upregulated LDLR expression in A549 and H460 cells, which may be attributable to intracellular lipid accumulation. Knockdown of LDLR reduced intracellular cholesterol content, but interestingly, anlotinib significantly improved intracellular cholesterol accumulation in LDLR-knockdown cells. Both exogenous LDL and LDLR knockdown decreased the sensitivity of cells to anlotinib. CONCLUSIONS: Anlotinib modulates host lipid metabolism through multiple pathways. Anlotinib also exerts a significant impact on lipid metabolism in cancer cells by regulating key transcription factors and metabolic enzymes. In addition, these findings suggest lipid metabolism is implicated in anlotinib sensitivity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-023-01907-y. BioMed Central 2023-08-23 /pmc/articles/PMC10464365/ /pubmed/37612751 http://dx.doi.org/10.1186/s12944-023-01907-y Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhu, Zhongling
Xu, Shan
Ren, Jing
Jiang, Teng
Zhang, Cai
Yan, Zhao
Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells
title Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells
title_full Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells
title_fullStr Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells
title_full_unstemmed Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells
title_short Anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells
title_sort anlotinib affects systemic lipid metabolism and induces lipid accumulation in human lung cancer cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464365/
https://www.ncbi.nlm.nih.gov/pubmed/37612751
http://dx.doi.org/10.1186/s12944-023-01907-y
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