Skip to main content
. 2023 Jul 22;42:177. doi: 10.1186/s13046-023-02729-7

Table 1.

Interaction between resident liver cells and cancer cells

Resident cells Interacting molecule(s) Major effects
LSECs Mannose receptor and scavenger receptor Internalise, process and transfer antigens through MHC I and MHC II to T cells
PD-L1–PD-1 Induce CD8+ T-cell tolerance to trigger immune escape of cancer cells
IFNγ, NO and Fas–FasL Induce apoptosis of cancer cells
CXCL16 Recruit NKT cells to fight cancer cells
E-selectin, VCAM-1, ICAM-1, sialyl Lewis-x, PSGL-1 and ESL-1 Facilitate the adherence of cancer cells to LSECs and their migration into the space of Disse to protect them from elimination
LSECtin Suppress T-cell immune responses and promote the adhesion and metastasis of CRC to the liver
KCs TNF-α, IL-1α and IL-1β Phagocytose and eliminate disseminated cancer cells
MHC II and PD-L1–PD-1 Expand Treg cells to induce an immune-tolerant environment
TGF-β, fibronectin, EGF, VEGF, MMP-2, MMP-9 and MMP-13 Lead to ECM remodelling, angiogenesis and cancer progression
Exosomal miR-135a-5p Mediate immunosuppression and facilitate the formation of a pre-metastatic niche
HSCs TGF-β, fibronectin, EGF, VEGF, MMP-2, MMP-9, and MMP-13 Lead to ECM remodelling, angiogenesis and cancer progression
TGF-β Promote ECM remodelling
Exosomal miR-181a-5p Facilitate CRLM by activating HSCs
Hepatocytes Integrins or desmosomes Mediate the adhesion of CRC cells to hepatocytes
Integrins and heregulin Boost the migration and LM of CRC
SAA Reshape the hepatic immune and fibrogenic microenvironment to promote LM
IGF-1 Promote cancer growth and metastasis

MHC I Major histocompatibility complex class I, MHC II Major histocompatibility complex class II, SAA Serum amyloid A1 and A2,  IGF-1 Insulin-like growth factor-I