Literature DB >> 33508529

MDSCs in liver cancer: A critical tumor-promoting player and a potential therapeutic target.

Chi Ma1, Qianfei Zhang1, Tim F Greten2.   

Abstract

Liver cancer is a leading cause of cancer deaths worldwide. Hepatocellular carcinoma (~75-85%) and cholangiocarcinoma (~10-15%) account for the majority of primary liver malignancies. Patients with primary liver cancer are often diagnosed with unresectable diseases and do not respond well to current therapies. The liver is also a common site of metastasis. Liver metastasis is difficult to treat, and the prognosis is poor. Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of immature myeloid cells with immunosuppressive activity. MDSCs are an important component of the tumor microenvironment and promote tumor progression through various mechanisms. MDSCs expand in both liver cancer patients and mouse liver cancer models. Importantly, MDSCs correlate with poor clinical outcomes for liver cancer patients. The tumor-promoting functions of MDSCs have also been shown in mouse liver cancer models. All these studies suggest that targeting MDSCs can potentially benefit liver cancer treatment. This review summarizes the current findings of MDSC regulation in liver cancer and related disease conditions. Published by Elsevier Inc.

Entities:  

Keywords:  Liver cancer; MDSCs; Tumor immunology

Mesh:

Substances:

Year:  2021        PMID: 33508529      PMCID: PMC7882059          DOI: 10.1016/j.cellimm.2021.104295

Source DB:  PubMed          Journal:  Cell Immunol        ISSN: 0008-8749            Impact factor:   4.868


  98 in total

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Journal:  Cancer Immunol Immunother       Date:  2019-10-23       Impact factor: 6.968

3.  Atezolizumab plus Bevacizumab in Unresectable Hepatocellular Carcinoma.

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Journal:  N Engl J Med       Date:  2020-05-14       Impact factor: 91.245

Review 4.  The Nature of Myeloid-Derived Suppressor Cells in the Tumor Microenvironment.

Authors:  Vinit Kumar; Sima Patel; Evgenii Tcyganov; Dmitry I Gabrilovich
Journal:  Trends Immunol       Date:  2016-02-06       Impact factor: 16.687

Review 5.  Myeloid-derived suppressor cells and anti-tumor T cells: a complex relationship.

Authors:  Ngozi R Monu; Alan B Frey
Journal:  Immunol Invest       Date:  2012       Impact factor: 3.657

Review 6.  The Role of Angiogenesis in Hepatocellular Carcinoma.

Authors:  Michael A Morse; Weijing Sun; Richard Kim; Aiwu Ruth He; Paolo B Abada; Michelle Mynderse; Richard S Finn
Journal:  Clin Cancer Res       Date:  2018-10-01       Impact factor: 12.531

7.  Increased circulating Lin(-/low) CD33(+) HLA-DR(-) myeloid-derived suppressor cells in hepatocellular carcinoma patients.

Authors:  Peng Shen; Aijuan Wang; Mengye He; Qingqing Wang; Shusen Zheng
Journal:  Hepatol Res       Date:  2013-07-10       Impact factor: 4.288

Review 8.  From NASH to HCC: current concepts and future challenges.

Authors:  Quentin M Anstee; Helen L Reeves; Elena Kotsiliti; Olivier Govaere; Mathias Heikenwalder
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2019-07       Impact factor: 46.802

9.  PD-L1 is a novel direct target of HIF-1α, and its blockade under hypoxia enhanced MDSC-mediated T cell activation.

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Journal:  J Exp Med       Date:  2014-04-28       Impact factor: 14.307

10.  Fibroblastic FAP promotes intrahepatic cholangiocarcinoma growth via MDSCs recruitment.

Authors:  Yuli Lin; Bingji Li; Xuguang Yang; Qian Cai; Weiren Liu; Mengxin Tian; Haoyang Luo; Wei Yin; Yan Song; Yinghong Shi; Rui He
Journal:  Neoplasia       Date:  2019-11-20       Impact factor: 5.715

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Journal:  Front Oncol       Date:  2022-06-13       Impact factor: 5.738

Review 2.  Role of immune escape in different digestive tumours.

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Journal:  World J Clin Cases       Date:  2021-12-06       Impact factor: 1.337

Review 3.  The role of the tumor microbe microenvironment in the tumor immune microenvironment: bystander, activator, or inhibitor?

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4.  Effect of Transdermal Fentanyl Patch Combined with Enhanced Recovery after Surgery on the Curative Effect and Analgesic Effect of Liver Cancer.

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Journal:  Biomed Res Int       Date:  2022-07-25       Impact factor: 3.246

5.  A high throughput method for Monitoring of Sorafenib, regorafenib, cabozantinib and their metabolites with UPLC-MS/MS in rat plasma.

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Journal:  Front Pharmacol       Date:  2022-09-08       Impact factor: 5.988

  5 in total

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