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We began analyzing https://link.springer.com/article/10.1007/s11912-022-01223-1, but it redirected us to https://link.springer.com/article/10.1007/s11912-022-01223-1. The analysis below is for the second page.

Title[redir]:
Fatty Acid Metabolism and Cancer Immunotherapy | Current Oncology Reports
Description:
Purpose of Review In this review, we update the latest findings on the impacts of FA metabolism reprogramming on the phenotypes and functions of immune cells in tumor-related immune responses. We also summarize the combinatorial interventions of FA metabolism, which improve the effects of current immunotherapies. Recent Findings Multiple studies have shown that either the abnormality in signaling pathways or nutrition competition in the TME can lead to phenotypic reprogramming of FA metabolism and functional changes in tumor-infiltrating immune cells, thereby influencing the therapeutic effects of cancer immunotherapies. Accordingly, regulating FA metabolism in immune cells has emerged and become promising approaches to synergize with immunotherapies. Summary One of the mechanisms behind suboptimal therapeutic effects of immunotherapies is metabolic reprogramming of the TME that impairs immunosuppressive activity. FA metabolism is a crucial process involved in the survival and function of primary immune cells. It is of great significance to explore the feasibility of overcoming FA metabolic barriers to improve cancer immunotherapy.

Matching Content Categories {πŸ“š}

  • Health & Fitness
  • Science
  • Education

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Custom-built

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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We don't see any clear sign of profit-making.

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Keywords {πŸ”}

pubmed, article, google, scholar, cas, cancer, central, cell, cells, metabolism, immunol, fatty, acid, metabolic, nat, immunotherapy, tumor, immune, httpsdoiorgs, immunity, wang, reprogramming, microenvironment, res, function, lipid, antitumor, memory, liu, wei, rev, oxidation, tcell, therapeutic, clin, biol, nature, zhang, dendritic, httpsdoiorgjimmuni, suppressor, content, current, review, responses, access, med, macrophages, myeloidderived, oncol,

Topics {βœ’οΈ}

antigen-specific cd4+cd25+foxp3+ regulatory gov/newsevents/newsroom/pressannouncements/ucm469571 month download article/chapter kinases tbk1-ikkvarepsilon supports resected mage-a3-positive t-cell receptor-engineered cell-derived interferon-gamma jia wei reviewed cancer immunotherapy immuno-oncology tumor-infiltrating immune cells potent tumor-specific lymphocytes mage-a3 cancer immunotherapeutic small-cell lung cancer activation-specific metabolic requirements myeloid-derived suppressor cells facilitates anti-pd-1 therapy tumor-related immune responses fatty acid oxidation anti-tumor therapeutic mab fatty acid synthesis srebp-controlled glucose metabolism fatty acid metabolism full article pdf high-fat diet srebp1-dependent metabolic fitness suppress anti-tumor immunity mtor regulate autophagy chowdhury ps jia wei fundamental research funds immuno-oncology rights immuno-oncology access cell-dependent antitumor activity al-khami aa impact anti-tumor immunity tumor milieu regulates impairs immunosuppressive activity privacy choices/manage cookies controls transcriptional programs de novo induction natural killer cells t-cell exhaustion enhances cancer therapies myeloid suppressor cells author information authors immunometabolic regulations mediated leptin metabolically licenses central universities cell immune responses obesity shapes metabolism

Schema {πŸ—ΊοΈ}

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         description:In this review, we update the latest findings on the impacts of FA metabolism reprogramming on the phenotypes and functions of immune cells in tumor-related immune responses. We also summarize the combinatorial interventions of FA metabolism, which improve the effects of current immunotherapies. Multiple studies have shown that either the abnormality in signaling pathways or nutrition competition in the TME can lead to phenotypic reprogramming of FA metabolism and functional changes in tumor-infiltrating immune cells, thereby influencing the therapeutic effects of cancer immunotherapies. Accordingly, regulating FA metabolism in immune cells has emerged and become promising approaches to synergize with immunotherapies. One of the mechanisms behind suboptimal therapeutic effects of immunotherapies is metabolic reprogramming of the TME that impairs immunosuppressive activity. FA metabolism is a crucial process involved in the survival and function of primary immune cells. It is of great significance to explore the feasibility of overcoming FA metabolic barriers to improve cancer immunotherapy.
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