肝脏 ›› 2025, Vol. 30 ›› Issue (12): 1642-1646.

• 肝肿瘤 • 上一篇    下一篇

肝细胞癌组织中PRMT5、ADAM17表达及临床意义分析

戴译萱, 朱洁, 杨晶晶, 王秋蕾   

  1. 215600 张家港 张家港市第一人民医院病理科
  • 收稿日期:2025-03-19 发布日期:2026-02-10
  • 通讯作者: 朱洁,Email:570100804@qq.com
  • 基金资助:
    苏州市医疗卫生科技创新项目(SKYD2023053)

An analysis on the expression and clinical significance of PRMT5 and ADAM17 in hepatocellular carcinoma tissue

DAI Yi-xuan, ZHU Jie, YANG Jing-jing, WANG Qiu-lei   

  1. Department of Pathology, Zhangjiagang First People's Hospital, Zhangjiagang 215600, China
  • Received:2025-03-19 Published:2026-02-10
  • Contact: ZHU Jie, Email : 570100804@qq.com

摘要: 目的 分析肝细胞癌(HCC)组织中组蛋白精氨酸甲基转移酶5(PRMT5)、去整合素金属蛋白酶17(ADAM17)表达及临床意义。方法 收集我院2018年9月至2021年9月病理科存档的HCC患者术后癌组织98例及对应癌旁组织77例。免疫组化法检测HCC组织及癌旁组织PRMT5、ADAM17表达,并进一步分析其临床意义。结果 PRMT5在HCC组织中的阳性表达率为56.12%(55/98),癌旁组织中为15.58%(12/77),ADAM17在HCC组织中的阳性表达率为65.31%(64/98),癌旁组织中为9.09%(7/77),两者在HCC组织中的阳性表达率均较癌旁组织显著升高(P<0.001)。HCC患者PRMT5、ADAM17均与肿瘤直径、分化程度、淋巴结转移、TNM分期、AFP水平相关,且PRMT5表达还与肝硬化有关(P<0.05)。PRMT5阳性表达患者3年生存率为18.18%(10/55),阴性表达患者为58.14%(25/43),ADAM17阳性表达患者3年生存率为26.56%(17/64),阴性表达患者为52.94%(18/34),PRMT5、ADAM17阳性表达患者3年生存率均较阴性表达患者明显降低(P<0.05)。多因素Cox回归分析显示,分化程度(OR=1.892,95%CI:1.063~3.345,P<0.001)、淋巴结转移(OR=1.964,95%CI:1.102~3.457,P<0.001)、TNM分期(OR=2.011,95%CI:1.473~4.152,P<0.001)、PRMT5表达(OR=2.100,95%CI:1.657~3.410,P<0.001)及ADAM17表达(OR=2.457,95%CI:1.974~3.469,P<0.001)均可独立影响HCC患者预后。经Pearson相关性分析发现,HCC患者癌组织PRMT5与ADAM17呈正相关(r=0.549,P<0.05)。结论 HCC组织中PRMT5、ADAM17均呈阳性表达,且与肿瘤直径、分化程度等临床病理特征相关。PRMT5、ADAM17阳性表达HCC患者生存率较低,有望作为评估患者预后的重要指标。

关键词: 肝细胞癌, 组蛋白精氨酸甲基转移酶5, 去整合素金属蛋白酶17, 临床病理特征, 预后

Abstract: Objective To analyze the expression and clinical significance of histone arginine methyltransferase 5 (PRMT5) and disintegrin metalloproteinase 17 (ADAM17) in hepatocellular carcinoma (HCC) tissues. Methods Ninety-eight postoperative cancer tissues and 77 corresponding adjacent tissues from HCC patients archived in the department of pathology of Zhangjiagang First People's Hospital from September 2018 to September 2021 were collected. The expression of PRMT5 and ADAM17 in HCC and adjacent tissues was detect with Immunohistochemistry, and their clinical significance was further analyzed. Results The positive expression rate of PRMT5 and ADAM17 was 56.12% (55/98) and 65.31% (64/98) in HCC tissues and 15.58% (12/77) and 9.09% (7/77) in para-cancerous tissues, res[ectively, both of which were significantly higher in HCC tissues compared with para-cancerous tissues (P<0.001). Both PRMT5 and ADAM17 in HCC patients were correlated with tumor diameter, degree of differentiation, lymph node metastasis, Tumor-Lymph nodes-Metastasis (TNM) stage, and alpha-fetoprotein (AFP) level. Moreover, PRMT5 expression was associated with cirrhosis (P<0.05). The 3-year survival rates of patients with positive expression of PRMT5 and ADAM17 were 18.18% (10/55) and 26.56% (17/64), respectively, which were significantly lower than those of 58.14% (25/43) and 52.94% (18/34) in patients with negative expression (P<0.05). Multifactorial Cox regression analysis showed that the degree of differentiation (OR=1.892, 95% CI: 1.063~3.345, P<0.001), lymph node metastasis (OR=1.964, 95%CI: 1.102~3.457, P<0.001), TNM stage (OR=2.011, 95%CI: 1.473~4.152, P<0.001), PRMT5 expression (OR=2.100, 95%CI: 1.657~3.410, P<0.001) and ADAM17 expression (OR=2.457, 95%CI: 1.974~3.469, P<0.001) were independent factors associated with the prognosis of HCC patients. Pearson correlation analysis found that in cancer tissues of HCC patients, The expression level of PRMT5 was positively correlated with that of ADAM17 (r=0.549, P<0.05). Conclusion PRMT5 and ADAM17 are both positively expressed in HCC tissues and are correlated with clinical pathological features such as tumor diameter and differentiation degree. Patients with HCC who positively express PRMT5 and ADAM17 have a lower survival rate and thus they may serve as important indicators for evaluating patient prognosis.

Key words: Hepatocellular carcinoma, Protein arginine methyltransferases 5, A disintegrin and metalloprotease 17, Clinical and pathological features, Prognosis