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The role of myeloid-derived suppressor cells in liver cancer.

作者信息

Zhou Shiyue, Zhao Zixuan, Zhong Hao, Ren Zehao, Li Yuye, Wang Hong, Qiu Yuling

机构信息

State Key Laboratory of Component-based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, 10 Poyanghu Road, Jinghai District, Tianjin, 301617, People's Republic of China.

School of Medical Technology, Tianjin University of Traditional Chinese Medicine, 10 Poyanghu Rd., West Area, Tuanbo New Town, Jinghai Dist, Tianjin, 301617, China.

出版信息

Discov Oncol. 2023 May 23;14(1):77. doi: 10.1007/s12672-023-00681-8.


DOI:10.1007/s12672-023-00681-8
PMID:37217620
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10203092/
Abstract

MDSCs are immature myeloid immune cells, which accumulate in models of liver cancer to reduce effector immune cell activity, contribute to immune escape and treatment resistance. The accumulation of MDSCs suppresses the role of CTL and the killing effects of NK cells, induces the accumulation of Treg cells, and blocks the antigen presentation of DCs, thus promoting the progression of liver cancer. Recently, immunotherapy has emerged a valuable approach following chemoradiotherapy in the therapy of advanced liver cancer. A considerable increasing of researches had proved that targeting MDSCs has become one of the therapeutic targets to enhance tumor immunity. In preclinical study models, targeting MDSCs have shown encouraging results in both alone and in combination administration. In this paper, we elaborated immune microenvironment of the liver, function and regulatory mechanisms of MDSCs, and therapeutic approaches to target MDSCs. We also expect these strategies to supply new views for future immunotherapy for the treatment of liver cancer.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/bd90f4f699fa/12672_2023_681_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/74e85d6a0886/12672_2023_681_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/bd90f4f699fa/12672_2023_681_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/74e85d6a0886/12672_2023_681_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/bd90f4f699fa/12672_2023_681_Fig2_HTML.jpg

相似文献

[1]
The role of myeloid-derived suppressor cells in liver cancer.

Discov Oncol. 2023-5-23

[2]
Immunotherapy Targeting Myeloid-Derived Suppressor Cells (MDSCs) in Tumor Microenvironment.

Front Immunol. 2021-2-4

[3]
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Blood Rev. 2016-9

[4]
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J Hepatol. 2018-11-9

[5]
Myeloid-derived suppressor cells in cancer: therapeutic targets to overcome tumor immune evasion.

Exp Hematol Oncol. 2024-4-12

[6]
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Signal Transduct Target Ther. 2021-10-7

[7]
Myeloid-Derived Suppressor Cells: A New and Pivotal Player in Colorectal Cancer Progression.

Front Oncol. 2020-12-15

[8]
The New Era of Cancer Immunotherapy: Targeting Myeloid-Derived Suppressor Cells to Overcome Immune Evasion.

Front Immunol. 2020

[9]
Nanoparticle Systems Modulating Myeloid-Derived Suppressor Cells for Cancer Immunotherapy.

Curr Top Med Chem. 2017

[10]
Suppression of T cells by myeloid-derived suppressor cells in cancer.

Hum Immunol. 2017-2

引用本文的文献

[1]
Targeting YTHDF2 with pH-responsive siRNA nanoparticles suppresses MYC m6A modification and restores antitumor immunity in hepatocellular carcinoma.

J Nanobiotechnology. 2025-7-1

[2]
Spatial‒temporal heterogeneities of liver cancer and the discovery of the invasive zone.

Clin Transl Med. 2025-2

[3]
Increased CD14HLA-DR myeloid-derived suppressor cells can be regarded as a biomarker on disease severity and response to therapy in acute coronary syndrome.

PeerJ. 2024

[4]
Dietary vitamin B3 supplementation induces the antitumor immunity against liver cancer via biased GPR109A signaling in myeloid cell.

Cell Rep Med. 2024-9-17

[5]
IMbrave152/SKYSCRAPER-14: a Phase III study of atezolizumab, bevacizumab and tiragolumab in advanced hepatocellular carcinoma.

Future Oncol. 2024

[6]
Overcoming Resistance to Immune Checkpoint Blockade in Liver Cancer with Combination Therapy: Stronger Together?

Semin Liver Dis. 2024-5

[7]
NamiRNA-mediated high expression of KNSTRN correlates with poor prognosis and immune infiltration in hepatocellular carcinoma.

Contemp Oncol (Pozn). 2023

[8]
Advances in Immunotherapy for Hepatocellular Carcinoma (HCC).

Curr Oncol. 2023-11-7

[9]
Innate Immunity in Cancer Biology and Therapy.

Int J Mol Sci. 2023-7-8

本文引用的文献

[1]
Neutralization of NET-associated human ARG1 enhances cancer immunotherapy.

Sci Transl Med. 2023-3-15

[2]
"Open Sesame" to the complexity of pattern recognition receptors of myeloid-derived suppressor cells in cancer.

Front Immunol. 2023

[3]
Functional states of myeloid cells in cancer.

Cancer Cell. 2023-3-13

[4]
Therapeutic targeting of tumour myeloid cells.

Nat Rev Cancer. 2023-4

[5]
Stromal Reprogramming through Dual PDGFRα/β Blockade Boosts the Efficacy of Anti-PD-1 Immunotherapy in Fibrotic Tumors.

Cancer Res. 2023-3-2

[6]
Ferroptosis of tumour neutrophils causes immune suppression in cancer.

Nature. 2022-12

[7]
Myeloid-derived itaconate suppresses cytotoxic CD8 T cells and promotes tumour growth.

Nat Metab. 2022-12

[8]
Myeloid-derived suppressor cells: an emerging target for anticancer immunotherapy.

Mol Cancer. 2022-9-26

[9]
Immunomodulatory activity of polysaccharides from by activating Akt/NF-κB signaling.

Chin Herb Med. 2021-10-7

[10]
He-Wei Granule enhances anti-tumor activity of cyclophosphamide by changing tumor microenvironment.

Chin Herb Med. 2021-10-7

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