Page 267 - Read Online
P. 267

Qin et al. Hepatoma Res 2020;6:24  I  http://dx.doi.org/10.20517/2394-5079.2020.04                                                 Page 13 of


               atezolizumab are targeting PD-1/PD-L1 or CTLA-4, and there have been encouraging results for a variety of
               tumors. However, phase III clinical research is still lacking, and more clinical research is urgently needed.


               In addition, the results of the present study indicate that the effect of single immunotherapy on liver
               cancer remains limited. The indication of immunotherapy in HCC may depend on combination therapies.
               Combination of liver-targeted therapy and immunotherapy can enhance tumor and systemic immune
               response. In conclusion, the advent of immunotherapy revolutionized cancer therapy and brought treatment
               for HCC to a brand-new period.


               DECLARATIONS
               Authors’ contributions
               Study concept and design: Xu XD
               Literature search: Qin W
               Drafting of the manuscript: Qin W, Cao ZY, Liu SY
               Critical revision of the manuscript for important intellectual content: Xu XD

               Availability of data and materials
               Not applicable.

               Financial support and sponsorship
               This study was funded by the National Natural Science Foundation of China (grant number 81670111).


               Conflicts of interest
               All authors declared that there are no conflicts of interest.

               Ethical approval and consent to participate
               Not applicable.


               Consent for publication
               Not applicable.


               Copyright
               © The Author(s) 2020.


               REFERENCES
               1.   Akinyemiju T, Abera S, Ahmed M, Alam N, Alemayohu MA, et al.; Global Burden of Disease Liver Cancer Collaboration. The burden
                   of primary liver cancer and underlying etiologies from 1990 to 2015 at the global, regional, and national level: results from the global
                   burden of disease study 2015. JAMA Oncol 2017;3:1683-91.
               2.   Forner A, Reig M, Bruix J. Hepatocellular carcinoma. Lancet 2018;391:1301-14.
               3.   Fujimoto A, Totoki Y, Abe T, Boroevich KA, Hosoda F, et al. Whole-genome sequencing of liver cancers identifies etiological
                   influences on mutation patterns and recurrent mutations in chromatin regulators. Nat Genet 2012;44:760-4.
               4.   Hilmi M, Vienot A. Immune therapy for liver cancers. Cancers (Basel) 2019;12:77.
               5.   Gao B, Jeong WI, Tian Z. Liver: an organ with predominant innate immunity. Hepatology 2008;47:729-36.
                                                                            +
               6.   Shalapour S, Lin XJ, Bastian IN, Brain J, Burt AD, et al. Inflammation-induced IgA  cells dismantle anti-liver cancer immunity.
                   Nature 2017;551:340-5.
               7.   Movahedi K, Laoui D, Gysemans C, Baeten M, Stange G, et al. Different tumor microenvironments contain functionally distinct
                   subsets of macrophages derived from Ly6C(high) monocytes. Cancer Res 2010;70:5728-39.
               8.   Mantovani A, Allavena P. The interaction of anticancer therapies with tumor-associated macrophages. J Exp Med 2015;212:435-45.
               9.   Ye YC, Zhao JL, Lu YT, Gao CC, Yang Y, et al. NOTCH signaling via WNT regulates the proliferation of alternative, CCR2-
                   independent tumor-associated macrophages in hepatocellular carcinoma. Cancer Res 2019;79:4160-72.
               10.  Zhu F, Li X, Chen S, Zeng Q, Zhao Y, et al. Tumor-associated macrophage or chemokine ligand CCL17 positively regulates the
                   tumorigenesis of hepatocellular carcinoma. Med Oncol 2016;33:17.
               11.  Zhou SL, Zhou ZJ, Hu ZQ, Huang XW, Wang, Z, et al. Tumor-associated neutrophils recruit macrophages and T-regulatory cells to
   262   263   264   265   266   267   268   269   270   271   272