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Open AccessJournal ArticleDOI

Blocking Triggering Receptor Expressed on Myeloid Cells‐1‐Positive Tumor‐Associated Macrophages Induced by Hypoxia Reverses Immunosuppression and Anti‐Programmed Cell Death Ligand 1 Resistance in Liver Cancer

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TLDR
It is highlighted that the hypoxic environment initiated the onset of tumor immunosuppression through TREM‐1+ TAMs attracting CCR6+Foxp3+ Tregs, and TREM-1- TAMs endowed HCC with anti‐PD‐L1 therapy resistance.
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This article is published in Hepatology.The article was published on 2019-07-01 and is currently open access. It has received 147 citations till now. The article focuses on the topics: Tumor microenvironment & Tumor progression.

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Current perspectives on the immunosuppressive tumor microenvironment in hepatocellular carcinoma: challenges and opportunities.

TL;DR: The current concepts of immunosuppressive cells, including tumor-associated macrophages, marrow-derived suppressor cells, tumor- associated neutrophils, cancer-associated fibroblasts, and regulatory T cell interactions to actively promote tumorigenesis are discussed.
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Hepatic macrophages in liver homeostasis and diseases-diversity, plasticity and therapeutic opportunities.

TL;DR: Novel findings regarding the origins and functions of hepatic macrophages are highlighted, the potential of targeting macrophage subsets and their plasticity explain their different functional responses in distinct liver diseases are discussed.
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Targeting tumor-associated macrophages to synergize tumor immunotherapy.

TL;DR: In this paper, the authors summarize recent studies investigating the involvement of TAMs in immune checkpoint inhibition, tumor vaccines and adoptive cell transfer therapies, and discuss the therapeutic potential of targeting TAMs as an adjuvant therapy in tumor immunotherapies.
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Chemokines and the immune response to cancer.

TL;DR: In this paper, the role of the chemokine system in anti-tumor and Pro-Tumor immune responses is discussed and discussed how malignant cells and the tumor microenvironment regulate the overall chemokines landscape to shape the type and outcome of immune responses to cancer and cancer treatment.
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Targeted therapy for hepatocellular carcinoma: Challenges and opportunities.

TL;DR: The mechanism underlying the ineffectiveness of these targeted therapies, including oncogenic alterations in driver genes and downstream pathways, high heterogeneity of HCC, and the mutual interaction of tumor microenvironment that promotes therapeutic resistance are highlighted.
References
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Journal ArticleDOI

TIMER: A Web Server for Comprehensive Analysis of Tumor-Infiltrating Immune Cells

TL;DR: Tumor Immune Estimation Resource (TIMER) is presented to comprehensively investigate molecular characterization of tumor-immune interactions and provides a user-friendly web interface for dynamic analysis and visualization of these associations, which will be of broad utilities to cancer researchers.
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Tumor-associated macrophages: from mechanisms to therapy.

TL;DR: Therapeutic success in targeting these protumoral roles in preclinical models and in early clinical trials suggests that macrophages are attractive targets as part of combination therapy in cancer treatment.
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Tumour-associated macrophages as treatment targets in oncology

TL;DR: It is surmised that TAMs can provide tools to tailor the use of cytoreductive therapies and immunotherapy in a personalized medicine approach, and that TAM-focused therapeutic strategies have the potential to complement and synergize with both chemotherapy and immunotherapies.
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Hypoxia in cancer: significance and impact on clinical outcome

TL;DR: In this article, the authors suggest that hypoxia is prognostic for survival and local control in head and neck cancers, and use endogenous proteins (e.g., HIF-1α, GLUT-1, CA IX) or exogenous bioreductive drugs.
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