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©The Author(s) 2023.
World J Hepatol. Nov 27, 2023; 15(11): 1196-1209
Published online Nov 27, 2023. doi: 10.4254/wjh.v15.i11.1196
Published online Nov 27, 2023. doi: 10.4254/wjh.v15.i11.1196
Ref. | Macrophage cell type/phenotype | HCC cell lines/model/tissue | Exosome contents | Findings |
Liu et al[82], 2020 | THP-1/M2 | Human HCC cell lines: SK-HEP-1 and HepG2 cell; mouse HCC cell lines: Hepa 1-6 | MiR-92a-2-5p | Promote HCC invasion via altering the AR/PHLPP/p-AKT/β-catenin signaling |
Li et al[83], 2021 | THP-1/M2 | Human HCC cell lines: SMMC-7721 | MiR-15b | Promotes the progression of HCC by blocking the LATS1-mediated Hippo pathway |
Li et al[85], 2021 | THP-1/M2 | Human HCC cell lines: Huh7, 97H, HepG2, LM3 and SMMC-7721 | MiR-27a-3p | Promote cancer stemness of HCC via the miR-27a-3p/TXNIP pathways |
Tian et al[86], 2021 | THP-1/M2 | Human HCC cell lines: HepG2 and Bel-7402; human HCC tumor tissues | MiR-660-5p | Promote the development of HCC by regulating KLF3 |
Bai et al[88], 2020 | THP-1/M1 | Human HCC cell line BEL-7404, HepG2, SMMC-7721 and QGY-7703; Xenograft nude mouse model | MiR-326 | Suppresses HCC progression via NF-κB signaling pathway |
Pu J et al[89], 2021 | C57BL/6 mouse bone marrow-derived macrophages/M2 | Murine model of primary HCC (C57BL/6) | MiR-21-5p | Facilitate CD8+T cell exhaustion in HCC via the miR-21-5p/YOD1/YAP/β-catenin pathway |
Wang et al[90], 2019 | TAMs/M1 | Human HCC cell lines: Huh7, HepG2 and BEL-7404; human HCC tumor tissues | MiR-125a/b | Suppressed HCC cell proliferation and stem cell properties by targeting CD90 |
Zhang et al[92], 2022 | THP-1/M2 | Human HCC cell lines: SMMC-7721and HepG2; Xenograft nude mouse model (BALB/C) | hsa_circ_0004658 | Inhibits HCC progression via miR-499b-5p/JAM3 |
- Citation: Xiang SY, Deng KL, Yang DX, Yang P, Zhou YP. Function of macrophage-derived exosomes in chronic liver disease: From pathogenesis to treatment. World J Hepatol 2023; 15(11): 1196-1209
- URL: https://www.wjgnet.com/1948-5182/full/v15/i11/1196.htm
- DOI: https://dx.doi.org/10.4254/wjh.v15.i11.1196