实用医学杂志 ›› 2025, Vol. 41 ›› Issue (10): 1480-1486.doi: 10.3969/j.issn.1006-5725.2025.10.008

• 专题报道:肝癌 • 上一篇    

三白草酮调控Krüppel样因子5-促红细胞生成素肝细胞A2通路对肝癌细胞生长和免疫逃逸的影响

王山,万金良,赵中华,杨静,赵杰,郝延璋()   

  1. 滨州医学院附属医院肿瘤科 (山东 滨州 256603 )
  • 收稿日期:2025-02-08 出版日期:2025-05-25 发布日期:2025-05-21
  • 通讯作者: 郝延璋 E-mail:hyz022@126.com
  • 基金资助:
    山东省医学会临床科研项目(YXH2022ZX02124)

Effects of sauchinone regulating KLF5⁃EphA2 pathway on the growth and immune escape of hepatocellular carcinoma cells

Shan WANG,Jinliang WAN,Zhonghua ZHAO,Jing YANG,Jie ZHAO,Yanzhang. HAO()   

  1. Department of Oncology,Affiliated Hospital of Binzhou Medical College,Binzhou 256603,Shandong,China
  • Received:2025-02-08 Online:2025-05-25 Published:2025-05-21
  • Contact: Yanzhang. HAO E-mail:hyz022@126.com

摘要:

目的 探讨三白草酮(Sch)调节Krüppel样因子5(KLF5)-促红细胞生成素肝细胞A2(EphA2)通路对肝癌细胞生长和免疫逃逸的影响。 方法 Huh-7细胞分为肝癌组、Sch低、中、高剂量组(Sch-L组、Sch-M组、Sch-H组)、Sch-H + KLF5激活剂的阴性对照(OE-NC)组、Sch-H + KLF5激活剂(OE-KLF5)组。5-溴-2-脱氧尿嘧啶(EdU)染色和CCK-8、划痕实验、Transwll分别检测Huh-7细胞增殖、迁移、侵袭;Western blot检测Huh-7细胞中增殖性细胞核抗原(PCNA)、迁移侵袭增强子(MIEN1)、基质金属蛋白酶(MMP)-2、程序性死亡受体-配体1(PD-L1)、KLF5、EphA2蛋白。将上述6组Huh-7细胞分别与处于激活状态的CD8+ T细胞共同培养在96孔板中,并命名为肝癌共培养组、Sch-L共培养组、Sch-M共培养组、Sch-H共培养组、Sch-H + OE-NC共培养组、Sch-H + OE-KLF5共培养组,检测共培养体系中CD8+T细胞杀伤率及上清液中γ干扰素(IFN-γ)、白细胞介素(IL)-4、肿瘤坏死因子-α(TNF-α)水平。 结果 与肝癌组相比,Sch-L组、Sch-M组、Sch-H组EdU阳性率、OD450值、细胞侵袭数及PCNA、MIEN1、MMP-2、PD-L1、KLF5、EphA2蛋白降低,迁移距离变短(P < 0.05);与Sch-H组、Sch-H + OE-NC组相比,Sch-H + OE-KLF5组EdU阳性率、OD450值、细胞侵袭数及PCNA、MIEN1、MMP-2、PD-L1、KLF5、EphA2蛋白升高,迁移距离变长(P < 0.05)。与肝癌共培养组相比,Sch-L共培养组、Sch-M共培养组、Sch-H共培养组CD8+ T细胞对Huh-7细胞的杀伤率及上清液中IFN-γ、TNF-α、IL-4水平升高(P < 0.05);与Sch-H共培养组、Sch-H + OE-NC共培养组相比,Sch-H + OE-KLF5共培养组CD8+ T细胞对Huh-7细胞的杀伤率及上清液中IFN-γ、TNF-α、IL-4水平降低(P < 0.05) 结论 Sch可能通过抑制KLF5-EphA2通路抑制肝癌细胞生长和免疫逃逸。

关键词: 三白草酮, 肝癌, 免疫逃逸, Krüppel样因子5-促红细胞生成素肝细胞A2通路

Abstract:

Objective To investigate the effects of sauchinone (Sch) on the growth and immune escape of liver cancer cells by regulating the Krüppel like factor 5 (KLF5)-erythropoietin-producing hepatocellular receptor A2 (EphA2) pathway. Methods Huh-7 cells were grouped into liver cancer group, Sch low, medium, and high-dose groups (Sch-L group, Sch-M group, Sch-H group), Sch-H + KLF5 activator negative control group (OE-NC), and Sch-H + KLF5 activator (OE-KLF5) group. 5-bromo-2-deoxyuracil (EdU) staining, CCK-8, scratch assay, and Transwll were used to detect the proliferation, migration, and invasion of Huh-7 cells, respectively. Western blot was applied to detect proliferative cell nuclear antigen (PCNA), migration invasion enhancer(MIEN1), matrix metalloproteinase-2 (MMP-2), programmed death receptor ligand 1 (PD-L1), KLF5, and EphA2 proteins in Huh-7 cells. The Huh-7 cells in above 6 groups were co cultured with activated CD8+ T cells in a 96 well plate and named as liver cancer co culture group, Sch-L co culture group, Sch-M co culture group, Sch-H co culture group, Sch-H + OE-NC co culture group, and Sch-H + OE-KLF5 co culture group. The killing rate of CD8+T cells in the co culture system and the levels of interferon-γ (IFN-γ), interleukin-4 (IL-4), and tumor necrosis factor-α (TNF-α) in the supernatant were detected. Results Compared with the liver cancer group, the EdU positive rate, OD450 value, cell invasion number, and PCNA, MIEN1, MMP-2, PD-L1, KLF5, and EphA2 proteins in the Sch-L, Sch-M, and Sch-H groups reduced, the migration distance shorten (P < 0.05). Compared with the Sch-H group and Sch-H + OE-NC group, the EdU positive rate, OD450 value, cell invasion number, and PCNA, MIEN1, MMP-2, PD-L1, KLF5, and EphA2 proteins in the Sch-H + OE-KLF5 group increased, the migration distance prolonged (P < 0.05). Compared with the liver cancer co culture group, the killing rate of CD8+T cells on Huh-7 cells and the levels of IFN-γ, TNF-α, and IL-4 in the supernatant in the Sch-L co culture group, Sch-M co culture group, and Sch-H co culture group increased (P < 0.05). Compared with the Sch-H co culture group and the Sch-H + OE-NC co culture group, the killing rate of CD8+ T cells on Huh-7 cells and the levels of IFN-γ, TNF-α, and IL-4 in the supernatant in the Sch-H + OE-KLF5 co culture group decreased (P < 0.05). Conclusion Sch may inhibit growth and immune escape of liver cancer cells by inhibiting the KLF5-EphA2 pathway.

Key words: sauchinone, liver cancer, immune escape, krüppel like factor 5-erythropoietin-producing hepatocellular receptor A2 pathway

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