中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

癌旁组织二酯酰甘油激酶γ表达水平对肝细胞癌患者术后生存的影响

钱相君 郭正阳 王莉 聂涵笑 贺涛 王效谦 万百顺 姚明解 张玲

引用本文:
Citation:

癌旁组织二酯酰甘油激酶γ表达水平对肝细胞癌患者术后生存的影响

DOI: 10.3969/j.issn.1001-5256.2021.05.023
基金项目: 

河南省基础与前沿技术研究计划项目 (162300410108)

利益冲突声明:本研究不存在研究者、伦理委员会成员、受试者监护人以及与公开研究成果有关的利益冲突。
作者贡献声明:钱相君、郭正阳负责课题设计,收集数据,资料分析和撰写论文;王莉、聂涵笑参与收集数据;贺涛、王效谦、万百顺参与修改论文;姚明解、张玲负责拟定写作思路,指导撰写文章并最后定稿。
详细信息
    作者简介:

    钱相君(1990—),男,博士,主要从事病毒性肝炎和肝癌相关的研究

    郭正阳(1993—),女,博士,助理研究员,主要从事肝癌分子机制研究

    通信作者:

    姚明解,ymjnew@163.com

    张玲,zhanglily561@126.com

    二人对本文贡献相同,同为第一作者

  • 中图分类号: R735.7

Effect of the expression level of diacylglycerol kinase gamma in paracancerous tissue on postoperative survival in patients with hepatocellular carcinoma

  • 摘要:   目的  探究肝癌患者癌旁组织中二酯酰甘油激酶γ(DGKγ)的表达水平对术后生存的影响及临床价值。  方法  收集2008年12月—2012年8月郑州大学附属肿瘤医院收治的78例行手术切除的肝癌患者资料。实时荧光定量PCR检测癌旁组织中DGKγmRNA的表达水平,将78例患者分为低表达组(DGKγ<0.0862,简称LEP组)和高表达组(DGKγ≥0.0862,简称HEP组),比较2组间的基本资料特征。计量资料2组间比较使用t检验与Mann-Whitney U检验;计数资料2组间比较使用χ2检验。单因素和多因素Cox回归分析患者生存预后的独立影响因素;Kaplan-Meier法分析所有患者和巴塞罗那(BCLC)分期各亚组中LEP组和HEP组的生存情况。  结果  多因素Cox分析显示:癌旁DGKγ表达水平(HR=1.913,95%CI:1.111~3.296,P=0.019)、HBsAg(HR=2.645,95%CI:1.264~5.537,P=0.010)、Alb(HR=0.952,95%CI:0.916~0.990,P=0.013)、BCLC分期(HR=1.702,95%CI:1.267~2.286,P<0.001)、肿瘤大小(HR=1.083,95%CI:1.019~1.152,P=0.011)是肝癌患者术后长期生存的独立影响因素。78例患者中,LEP组的中位生存时间为45.0个月,显著高于HEP组的22.9个月(P=0.0025)。分层分析显示,BCLC A期中,LEP组的远期生存情况显著的优于HEP组(P=0.0345);B和C期中,LEP组和HEP组中位生存时间分别为16.5个月和10.8个月,2组间的近期和远期生存差异无统计学意义(P>0.05)。  结论  癌旁组织中DGKγ的表达水平可能是一种新的能够预测和评估肝癌患者术后长期生存风险的指标,具有一定的临床应用价值。

     

  • 图  1  癌旁DGKγ预测患者生存状态的ROC曲线

    图  2  Kaplan-Meier生存曲线比较

    注:a、c、d分别为所有患者、BCLC A期、BCLC B和C期中的LEP组与HEP组生存曲线;b为BCLC各期患者的生存曲线。

    表  1  癌旁组织DGKγ LEP组与HEP组的临床资料比较

    指标 总患者(n=78) LEP组(n=41) HEP组(n=37) 统计值 P
    年龄(岁) 54.32±10.74 55.17±10.62 53.38±10.94 t=0.734 0.465
    性别(男/女) 67/11 33/8 34/3 χ2=1.253 0.263
    HBsAg(阳性/阴性) 60/18 28/13 32/5 χ2=2.674 0.102
    AFP(ng/μl) 420.2(12.7~1210.0) 237.6(4.3~1039.0) 532.4(21.1~1210.0) Z=-1.621 0.105
    ALT(U/L) 38.0(25.0~63.3) 38.0(24.5~55.0) 38.0(25.5~70.5) Z=-0.280 0.779
    AST(U/L) 44.0(31.0~66.0) 42.0(32.0~60.0) 49.0(28.5~72.0) Z=-0.756 0.450
    ALP(U/L) 113.5(86.8~147.0) 123.0(90.0~153.0) 100.0(85.5~126.0) Z=-1.501 0.133
    GGT(U/L) 96.0(56.8~179.0) 117.0(50.5~191.7) 87.0(60.5~150.9) Z=-1.046 0.296
    TBil(μmol/L) 15.4(10.9~20.6) 15.5(11.4~20.5) 14.4(9.9~20.7) Z=-0.530 0.596
    Alb(g/L) 39.88±6.61 39.71±7.77 40.08±5.11 t=-0.247 0.806
    Glb(g/L) 29.56±6.34 30.07±5.79 28.99±6.93 t=0.751 0.455
    RBC(×1012/L) 4.31±0.63 4.36±0.59 4.25±0.66 t=0.775 0.441
    PLT(×109/L) 151(104~200) 167(113~212) 140(102~186) Z=-1.256 0.209
    PT(s) 13.4(12.1~14.4) 13.0(11.7~14.4) 13.7(12.7~14.7) Z=-1.987 0.047
    INR 1.15(1.02~1.23) 1.10(0.99~1.25) 1.16(1.08~1.23) Z=-1.392 0.164
    FIB(g/L) 3.00±0.85 3.02±0.93 2.97±0.76 t=0.097 0.767
    Child-Pugh分级(A/B) 69/9 38/3 31/6 χ2=0.763 0.382
    术中输血(是/否) 26/52 12/29 14/23 χ2=0.643 0.423
    BCLC分期(A/B/C) 44/10/24 27/4/10 17/6/14 χ2=3.143 0.208
    肿瘤大小(cm) 7.0(5.0~11.0) 7.0(4.5~12.0) 8.0(5.0~10.5) Z=-0.431 0.666
    肿瘤数目(1个/≥2个) 58/20 33/8 25/12 χ2=1.703 0.192
    切缘(是/否) 48/30 26/15 22/15 χ2=0.129 0.720
    下载: 导出CSV

    表  2  所有患者生存预后的单因素分析

    指标 HR(95%CI) P
    年龄(岁) 0.984(0.960~1.008) 0.186
    性别(男/女) 0.775(0.381~1.577) 0.482
    HBsAg(阳性/阴性) 2.376(1.198~4.710) 0.013
    AFP(ng/μl) 1.001(1.000~1.001) 0.016
    ALT(U/L) 1.001(1.000~1.001) 0.293
    AST(U/L) 1.001(1.000~1.001) 0.088
    ALP(U/L) 1.004(1.000~1.008) 0.080
    GGT(U/L) 1.002(1.000~1.004) 0.063
    TBil(μmol/L) 0.994(0.966~1.022) 0.660
    Alb(g/L) 0.953(0.926~0.981) 0.001
    Glb(g/L) 1.007(0.967~1.048) 0.749
    RBC(×1012/L) 0.817(0.508~1.314) 0.405
    PLT(×109/L) 1.003(1.000~1.006) 0.037
    PT(s) 1.059(0.945~1.186) 0.324
    INR 2.649(0.825~8.508) 0.102
    FIB(g/L) 1.338(0.999~1.791) 0.051
    Child-Pugh分级(A/B) 1.517(0.718~3.203) 0.275
    术中输血(是/否) 2.430(1.437~4.111) 0.001
    BCLC分期(A/B/C) 2.033(1.532~2.699) <0.001
    肿瘤大小(cm) 1.088(1.030~1.148) 0.002
    肿瘤数目(1个/≥2个) 1.814(1.039~3.167) 0.036
    切缘(是/否) 1.859(1.112~3.107) 0.018
    癌旁DGKγ (HEP/LEP) 2.188(1.302~3.677) 0.003
    下载: 导出CSV
  • [1] BRAY F, FERLAY J, SOERJOMATARAM I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J]. CA Cancer J Clin, 2018, 68(6): 394-424. DOI: 10.3322/caac.21492.
    [2] TORRE LA, BRAY F, SIEGEL RL, et al. Global cancer statistics, 2012[J]. CA Cancer J Clin, 2015, 65(2): 87-108. DOI: 10.3322/caac.21262.
    [3] ZHOU M, WANG H, ZENG X, et al. Mortality, morbidity, and risk factors in China and its provinces, 1990-2017: A systematic analysis for the Global Burden of Disease Study 2017[J]. Lancet, 2019, 394(10204): 1145-1158. DOI: 10.1016/S0140-6736(19)30427-1.
    [4] LIU AX, WANG HQ, BO WT, et al. Clinical efficacy and prognostic factors analysis of hepatectomy for hepatocellular carcinoma[J]. Chin J Dig Surg, 2019, 18(4): 368-374. DOI: 10.3760/cma.j.issn.1673-9752.2019.04.012.

    刘爱祥, 王海清, 薄文滔, 等. 肝细胞癌肝切除术的临床疗效及预后因素分析[J]. 中华消化外科杂志, 2019, 18(4): 368-374. DOI: 10.3760/cma.j.issn.1673-9752.2019.04.012.
    [5] European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma[J]. J Hepatol, 2018, 69(1): 182-236. DOI: 10.1016/j.jhep.2018.03.019.
    [6] Bureau of Medical Administration, National Health Commission of The People's Republic of China. Guidelines for diagnosis and treatment of primary liver cancer in China (2019 edition)[J]. J Clin Hepatol, 2020, 36(2): 277-292. DOI: 10.3969/j.issn.1001-5256.2020.02.007.

    中华人民共和国国家卫生健康委员会医政医管局. 原发性肝癌诊疗规范(2019年版)[J]. 临床肝胆病杂志, 2020, 36(2): 277-292. DOI: 10.3969/j.issn.1001-5256.2020.02.007.
    [7] QIAN XJ, QU CF, LU FM. The tumor markers of hepatocellular carcinoma play an indispensable role in ultrasound screening and monitoring early hepatocellular carcinoma[J]. Liver, 2019, 24(8): 851-853. DOI: 10.3969/j.issn.1008-1704.2019.08.003.

    钱相君, 曲春枫, 鲁凤民. 肝癌肿瘤标记物在超声筛查监测早期肝细胞癌中的作用不可或缺[J]. 肝脏, 2019, 24(8): 851-853. DOI: 10.3969/j.issn.1008-1704.2019.08.003.
    [8] HUANG C, FRETER C. Lipid metabolism, apoptosis and cancer therapy[J]. Int J Mol Sci, 2015, 16(1): 924-949. DOI: 10.3390/ijms16010924.
    [9] ARRANZ-NICOLÁS J, MÉRIDA I. Biological regulation of diacylglycerol kinases in normal and neoplastic tissues: New opportunities for cancer immunotherapy[J]. Adv Biol Regul, 2020, 75: 100663. DOI: 10.1016/j.jbior.2019.100663.
    [10] MÉRIDA I, TORRES-AYUSO P, ÁVILA-FLORES A, et al. Diacylglycerol kinases in cancer[J]. Adv Biol Regul, 2017, 63: 22-31. DOI: 10.1016/j.jbior.2016.09.005.
    [11] KAI M, YAMAMOTO E, SATO A, et al. Epigenetic silencing of diacylglycerol kinase gamma in colorectal cancer[J]. Mol Carcinog, 2017, 56(7): 1743-1752. DOI: 10.1002/mc.22631.
    [12] GUO Z, JIA J, YAO M, et al. Diacylglycerol kinase γ predicts prognosis and functions as a tumor suppressor by negatively regulating glucose transporter 1 in hepatocellular carcinoma[J]. Exp Cell Res, 2018, 373(1-2): 211-220. DOI: 10.1016/j.yexcr.2018.11.001.
    [13] HE Z, CHEN J, WANG J, et al. Expression of hepatitis B surface antigen in liver tissues can serve as a predictor of prognosis for hepatitis B virus-related hepatocellular carcinoma patients after liver resection[J]. Eur J Gastroenterol Hepatol, 2021, 33(1): 76-82. DOI: 10.1097/MEG.0000000000001698.
    [14] WANG L, LI Q, ZHANG J, et al. A novel prognostic scoring model based on albumin and γ-glutamyltransferase for hepatocellular carcinoma prognosis[J]. Cancer Manag Res, 2019, 11: 10685-10694. DOI: 10.2147/CMAR.S232073.
    [15] YAN X, YAO M, WEN X, et al. Elevated apolipoprotein B predicts poor postsurgery prognosis in patients with hepatocellular carcinoma[J]. Onco Targets Ther, 2019, 12: 1957-1964. DOI: 10.2147/OTT.S192631.
    [16] WU G, WU J, WANG B, et al. Importance of tumor size at diagnosis as a prognostic factor for hepatocellular carcinoma survival: A population-based study[J]. Cancer Manag Res, 2018, 10: 4401-4410. DOI: 10.2147/CMAR.S177663.
    [17] WU XF, LIU YW, ZHANG H, et al. Application value of different Barcelona clinical liver cancer Kinki staging in radical resection of liver cancer[J]. Chin J Dig Surg, 2020, 19(12): 1266-1272. DOI: 10.3760/cma.j.cn115610-20201102-00691.

    吴晓峰, 刘一纬, 张慧, 等. 不同巴塞罗那临床肝癌Kinki分期在肝癌根治术中的应用价值[J]. 中华消化外科杂志, 2020, 19(12): 1266-1272. DOI: 10.3760/cma.j.cn115610-20201102-00691.
    [18] MASSART J, ZIERATH JR. Role of diacylglycerol kinases in glucose and energy homeostasis[J]. Trends Endocrinol Metab, 2019, 30(9): 603-617. DOI: 10.1016/j.tem.2019.06.003.
    [19] RAINERO E, CIANFLONE C, PORPORATO PE, et al. The diacylglycerol kinase α/atypical PKC/β1 integrin pathway in SDF-1α mammary carcinoma invasiveness[J]. PLoS One, 2014, 9(6): e97144. DOI: 10.1371/journal.pone.0097144.
    [20] FILIGHEDDU N, SAMPIETRO S, CHIANALE F, et al. Diacylglycerol kinase α mediates 17-β-estradiol-induced proliferation, motility, and anchorage-independent growth of Hec-1A endometrial cancer cell line through the G protein-coupled estrogen receptor GPR30[J]. Cell Signal, 2011, 23(12): 1988-1996. DOI: 10.1016/j.cellsig.2011.07.009.
    [21] DOMINGUEZ CL, FLOYD DH, XIAO A, et al. Diacylglycerol kinase α is a critical signaling node and novel therapeutic target in glioblastoma and other cancers[J]. Cancer Discov, 2013, 3(7): 782-797. DOI: 10.1158/2159-8290.CD-12-0215.
    [22] BACCHIOCCHI R, BALDANZI G, CARBONARI D, et al. Activation of alpha-diacylglycerol kinase is critical for the mitogenic properties of anaplastic lymphoma kinase[J]. Blood, 2005, 106(6): 2175-2182. DOI: 10.1182/blood-2005-01-0316.
    [23] KONG Y, ZHENG Y, JIA Y, et al. Decreased LIPF expression is correlated with DGKA and predicts poor outcome of gastric cancer[J]. Oncol Rep, 2016, 36(4): 1852-1860. DOI: 10.3892/or.2016.4989.
    [24] MCMURRAY HR, SAMPSON ER, COMPITELLO G, et al. Synergistic response to oncogenic mutations defines gene class critical to cancer phenotype[J]. Nature, 2008, 453(7198): 1112-1116. DOI: 10.1038/nature06973.
    [25] TAKEISHI K, TAKETOMI A, SHIRABE K, et al. Diacylglycerol kinase alpha enhances hepatocellular carcinoma progression by activation of Ras-Raf-MEK-ERK pathway[J]. J Hepatol, 2012, 57(1): 77-83. DOI: 10.1016/j.jhep.2012.02.026.
  • 加载中
图(2) / 表(2)
计量
  • 文章访问数:  561
  • HTML全文浏览量:  111
  • PDF下载量:  34
  • 被引次数: 0
出版历程
  • 收稿日期:  2020-10-02
  • 录用日期:  2020-12-14
  • 出版日期:  2021-05-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回