2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Lipids in cancer: a global view of the contribution of lipid pathways to metastatic formation and treatment resistance

      review-article
      ,
      Oncogenesis
      Nature Publishing Group UK
      Cancer metabolism, Cancer microenvironment

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Lipids are essential constituents for malignant tumors, as they are absolutely required for tumor growth and dissemination. Provided by the tumor microenvironment (TME) or by cancer cells themselves through activation of de novo synthesis pathways, they orchestrate a large variety of pro-tumorigenic functions. Importantly, TME cells, especially immune cells, cancer-associated fibroblasts (CAFs) and cancer-associated adipocytes (CAAs), are also prone to changes in their lipid content, which hinder or promote tumor aggressiveness. In this review, we address the significant findings for lipid contribution in tumor progression towards a metastatic disease and in the poor response to therapeutic treatments. We also highlight the benefits of targeting lipid pathways in preclinical models to slow down metastasis development and overcome chemo-and immunotherapy resistance.

          Related collections

          Most cited references153

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          A framework for advancing our understanding of cancer-associated fibroblasts

          Cancer-associated fibroblasts (CAFs) are a key component of the tumour microenvironment with diverse functions, including matrix deposition and remodelling, extensive reciprocal signalling interactions with cancer cells and crosstalk with infiltrating leukocytes. As such, they are a potential target for optimizing therapeutic strategies against cancer. However, many challenges are present in ongoing attempts to modulate CAFs for therapeutic benefit. These include limitations in our understanding of the origin of CAFs and heterogeneity in CAF function, with it being desirable to retain some antitumorigenic functions. On the basis of a meeting of experts in the field of CAF biology, we summarize in this Consensus Statement our current knowledge and present a framework for advancing our understanding of this critical cell type within the tumour microenvironment.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Membrane lipids: where they are and how they behave.

            Throughout the biological world, a 30 A hydrophobic film typically delimits the environments that serve as the margin between life and death for individual cells. Biochemical and biophysical findings have provided a detailed model of the composition and structure of membranes, which includes levels of dynamic organization both across the lipid bilayer (lipid asymmetry) and in the lateral dimension (lipid domains) of membranes. How do cells apply anabolic and catabolic enzymes, translocases and transporters, plus the intrinsic physical phase behaviour of lipids and their interactions with membrane proteins, to create the unique compositions and multiple functionalities of their individual membranes?
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              NK Cells Stimulate Recruitment of cDC1 into the Tumor Microenvironment Promoting Cancer Immune Control

              Summary Conventional type 1 dendritic cells (cDC1) are critical for antitumor immunity, and their abundance within tumors is associated with immune-mediated rejection and the success of immunotherapy. Here, we show that cDC1 accumulation in mouse tumors often depends on natural killer (NK) cells that produce the cDC1 chemoattractants CCL5 and XCL1. Similarly, in human cancers, intratumoral CCL5, XCL1, and XCL2 transcripts closely correlate with gene signatures of both NK cells and cDC1 and are associated with increased overall patient survival. Notably, tumor production of prostaglandin E2 (PGE2) leads to evasion of the NK cell-cDC1 axis in part by impairing NK cell viability and chemokine production, as well as by causing downregulation of chemokine receptor expression in cDC1. Our findings reveal a cellular and molecular checkpoint for intratumoral cDC1 recruitment that is targeted by tumor-derived PGE2 for immune evasion and that could be exploited for cancer therapy.
                Bookmark

                Author and article information

                Contributors
                fabienne.guillaumond@inserm.fr
                Journal
                Oncogenesis
                Oncogenesis
                Oncogenesis
                Nature Publishing Group UK (London )
                2157-9024
                9 August 2022
                9 August 2022
                December 2022
                : 11
                : 1
                : 46
                Affiliations
                GRID grid.463833.9, ISNI 0000 0004 0572 0656, Centre de Recherche en Cancérologie de Marseille, INSERM, , Aix-Marseille Université, CNRS, Institut Paoli-Calmettes, ; F-13009 Marseille, France
                Author information
                http://orcid.org/0000-0002-2339-8854
                http://orcid.org/0000-0001-7456-7315
                Article
                420
                10.1038/s41389-022-00420-8
                9363460
                35945203
                16fec99a-419c-477a-a373-edb65035c6aa
                © The Author(s) 2022

                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/.

                History
                : 12 January 2022
                : 19 July 2022
                : 21 July 2022
                Funding
                Funded by: French National Cancer Institute (Pair Pancreas 2018-082) French foundation for Cancer Research (PGA 2020, PJA-20181208127) GEFLUC Marseille Provence & Canceropole PACA
                Funded by: French National Cancer Institute (Pair Pancreas 2018-082) French foundation for Cancer Research (PGA 2020, PJA-20181208127) GEFLUC Marseille Provence & Canceropole PACA
                Categories
                Review Article
                Custom metadata
                © The Author(s) 2022

                Oncology & Radiotherapy
                cancer metabolism,cancer microenvironment
                Oncology & Radiotherapy
                cancer metabolism, cancer microenvironment

                Comments

                Comment on this article