LI Jinyu,XU Xiaoyu,WANG Yuzhuo.Study on the mechanism of Lycium barbarum polysaccharides inhibiting the proliferation, migration and immune escape of oral cancer cells[J].ZHONGGUO YAOFANG,2025,36(17):2134-2140.
LI Jinyu,XU Xiaoyu,WANG Yuzhuo.Study on the mechanism of Lycium barbarum polysaccharides inhibiting the proliferation, migration and immune escape of oral cancer cells[J].ZHONGGUO YAOFANG,2025,36(17):2134-2140. DOI: 10.6039/j.issn.1001-0408.2025.17.09.
Study on the mechanism of Lycium barbarum polysaccharides inhibiting the proliferation, migration and immune escape of oral cancer cells
polysaccharides on the proliferation, migration, and immune escape of oral cancer cells by regulating the T cell immunoglobulin and mucin domain-containing protein 3 (TIM3)/galectin-9 (Gal-9) signaling pathway.
METHODS
2
Human oral cancer cells KB and CAL27 were assigned to control group,
L. barbarum
polysaccharides low-concentration group (200 μg/mL),
L. barbarum
polysaccharides high-concentration gr
oup (400 μg/mL), pcDNA-NC group (transfection of pcDNA-NC plasmid), pcDNA-TIM3 group (transfection of pcDNA-TIM3 plasmid), high concentration of
L. barbarum
polysaccharides+pcDNA-NC group (400 μg/mL
L. barbarum
polysaccharides + transfection of pcDNA-NC plasmid), and high concentration of
L. barbarum
polysaccharides+pcDNA-TIM3 group (400 μg/mL
L. barbarum
polysaccharides + transfection of pcDNA-TIM3 plasmid). The proliferation, migration and invasion abilities of the cells, T cell killing rate as well as the levels of interferon-γ (IFN-γ) and interleukin-2 (IL-2) in the cell supernatant were measured. mRNA expressions of TIM3 and Gal-9 and protein expressions of indoleamine 2,3-dioxygenase 1 (IDO1), programmed death-ligand 1 (PD-L1), TIM3 and Gal-9 in the cells were also determined.
RESULTS
2
Compared with control group, the clone formation rate, scratch healing rate, the number of invasive cells, protein expressions of IDO1 and PD-L1, mRNA and protein expressions of TIM3 and Gal-9 in both cell types of
L. barbarum
polysaccharide low- and high-concentration groups were decreased significantly (
P
<0.05), while the proliferation inhibition rate, T cell killing rate, and the levels of IFN-γ and IL-2 were significantly increased (
P
<0.05). Compared with control group and pcDNA-NC group, the clone formation rate, scratch healing rate, the number of invasive cells, and protein expressions of IDO1 and PD-L1, mRNA and protein expressions of TIM3 and Gal-9 in both cell types of the pcDNA-TIM3 group were all significantly increased (
P
<0.05), while the proliferation inhibition rate, T cell killing rate, IFN-γ and IL-2 levels were significantly decreased (
P
<0.05). Compared with
L. barbarum
polysaccharides high-concentration group and high concentration of
L. barbarum
polysaccharides+pcDNA-NC group, the clone fo
rmation rate, scratch healing rate, the number of invasive cells, and protein expressions of IDO1 and PD-L1, mRNA and protein expressions of TIM3 and Gal-9 in both cell types of high concentration of
L. barbarum
polysaccharides+pcDNA-TIM3 group were significantly increased (
P
<0.05), while the proliferation inhibition rate, T cell killing rate, and the levels of IFN-γ and IL-2 were significantly decreased (
P
<0.05).
CONCLUSIONS
2
L. barbarum
polysaccharides may inhibit the proliferation, migration, and immune escape of oral cancer cells by suppressing TIM3/Gal-9 signaling pathway.
关键词
Keywords
references
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