47
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Metabolic Cooperation and Competition in the Tumor Microenvironment: Implications for Therapy

      review-article

      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

          The tumor microenvironment (TME) is an ensemble of non-tumor cells comprising fibroblasts, cells of the immune system, and endothelial cells, besides various soluble secretory factors from all cellular components (including tumor cells). The TME forms a pro-tumorigenic cocoon around the tumor cells where reprogramming of the metabolism occurs in tumor and non-tumor cells that underlies the nature of interactions as well as competitions ensuring steady supply of nutrients and anapleoretic molecules for the tumor cells that fuels its growth even under hypoxic conditions. This metabolic reprogramming also plays a significant role in suppressing the immune attack on the tumor cells and in resistance to therapies. Thus, the metabolic cooperation and competition among the different TME components besides the inherent alterations in the tumor cells arising out of genetic as well as epigenetic changes supports growth, metastasis, and therapeutic resistance. This review focuses on the metabolic remodeling achieved through an active cooperation and competition among the three principal components of the TME—the tumor cells, the T cells, and the cancer-associated fibroblasts while discussing about the current strategies that target metabolism of TME components. Further, we will also consider the probable therapeutic opportunities targeting the various metabolic pathways as well as the signaling molecules/transcription factors regulating them for the development of novel treatment strategies for cancer.

          Related collections

          Most cited references226

          • Record: found
          • Abstract: not found
          • Article: not found

          On the origin of cancer cells.

          O WARBURG (1956)
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Fueling immunity: insights into metabolism and lymphocyte function.

            Lymphocytes face major metabolic challenges upon activation. They must meet the bioenergetic and biosynthetic demands of increased cell proliferation and also adapt to changing environmental conditions, in which nutrients and oxygen may be limiting. An emerging theme in immunology is that metabolic reprogramming and lymphocyte activation are intricately linked. However, why T cells adopt specific metabolic programs and the impact that these programs have on T cell function and, ultimately, immunological outcome remain unclear. Research on tumor cell metabolism has provided valuable insight into metabolic pathways important for cell proliferation and the influence of metabolites themselves on signal transduction and epigenetic programming. In this Review, we highlight emerging concepts regarding metabolic reprogramming in proliferating cells and discuss their potential impact on T cell fate and function.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Mitochondrial autophagy is an HIF-1-dependent adaptive metabolic response to hypoxia.

              Autophagy is a process by which cytoplasmic organelles can be catabolized either to remove defective structures or as a means of providing macromolecules for energy generation under conditions of nutrient starvation. In this study we demonstrate that mitochondrial autophagy is induced by hypoxia, that this process requires the hypoxia-dependent factor-1-dependent expression of BNIP3 and the constitutive expression of Beclin-1 and Atg5, and that in cells subjected to prolonged hypoxia, mitochondrial autophagy is an adaptive metabolic response which is necessary to prevent increased levels of reactive oxygen species and cell death.
                Bookmark

                Author and article information

                Contributors
                URI : http://frontiersin.org/people/u/427731
                URI : http://frontiersin.org/people/u/332912
                Journal
                Front Oncol
                Front Oncol
                Front. Oncol.
                Frontiers in Oncology
                Frontiers Media S.A.
                2234-943X
                12 April 2017
                2017
                : 7
                : 68
                Affiliations
                [1] 1Georgia Cancer Center, Augusta University , Augusta, GA, USA
                [2] 2School of Life Sciences, B. S. Abdur Rahman Crescent University , Chennai, India
                [3] 3Central Research Facility, Sri Ramachandra University , Chennai, India
                Author notes

                Edited by: Shanmugasundaram Ganapathy-Kanniappan, Johns Hopkins School of Medicine, USA

                Reviewed by: Egidio Iorio, Istituto Superiore di Sanità, Italy; Giorgio Stassi, University of Palermo, Italy

                *Correspondence: Seema Gupta, sgjija@ 123456gmail.com ; Amrita Roy, dr_amritaroy@ 123456yahoo.com ; Bilikere S. Dwarakanath, dwarakanath@ 123456sriramachandra.edu.in

                These authors have contributed equally to this work.

                Specialty section: This article was submitted to Cancer Molecular Targets and Therapeutics, a section of the journal Frontiers in Oncology

                Article
                10.3389/fonc.2017.00068
                5388702
                28447025
                8f2a0454-ff52-4cfc-984b-44da650b5390
                Copyright © 2017 Gupta, Roy and Dwarakanath.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 17 January 2017
                : 24 March 2017
                Page count
                Figures: 2, Tables: 1, Equations: 0, References: 338, Pages: 24, Words: 21790
                Categories
                Oncology
                Review

                Oncology & Radiotherapy
                tumor microenvironment,metabolic reprogramming,metabolic cooperation,warburg effect,cancer-associated fibroblasts,immune network,cancer cell metabolism

                Comments

                Comment on this article