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

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TLDR
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.
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 component 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 development of novel treatment strategies for cancer.

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The role of the crabtree effect and an endogenous fuel in the energy metabolism of resting and proliferating thymocytes

TL;DR: Rat thymocytes have been used to characterize the changes in energy metabolism that occur as cells undergo a resting/proliferation transition, indicating a profound Crabtree effect which is not present in resting cells.
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Tumour-elicited neutrophils engage mitochondrial metabolism to circumvent nutrient limitations and maintain immune suppression

TL;DR: It is shown that tumours promote neutrophils adapted to oxidative mitochondria metabolism that function in the glucose-restrained tumour microenvironment to promote tumour growth by maintaining local immune suppression.
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Regulation of T lymphocyte metabolism

TL;DR: The changes in cellular metabolism that accompany lymphocyte activation are discussed, with a particular emphasis on glucose metabolism, a major source of both energy and biosynthetic building blocks.
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Increased Serine Synthesis Provides an Advantage for Tumors Arising in Tissues Where Serine Levels Are Limiting

TL;DR: It is suggested that physiological serine availability restrains tumor growth and argued that tumors arising in serine-limited environments acquire a fitness advantage by upregulating serine synthesis pathway enzymes.
References
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Journal ArticleDOI

Hallmarks of cancer: the next generation.

TL;DR: Recognition of the widespread applicability of these concepts will increasingly affect the development of new means to treat human cancer.
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Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation

TL;DR: It is proposed that the metabolism of cancer cells, and indeed all proliferating cells, is adapted to facilitate the uptake and incorporation of nutrients into the biomass needed to produce a new cell.
Journal ArticleDOI

On the origin of cancer cells.

Origin of cancer cells

Otto Warburg
Journal ArticleDOI

Targeting HIF-1 for cancer therapy

TL;DR: Hypoxia-inducible factor 1 (HIF-1) activates the transcription of genes that are involved in crucial aspects of cancer biology, including angiogenesis, cell survival, glucose metabolism and invasion.
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