SVEP1 PKHD1 P53在原发性肝癌组织中的表达及其临床意义

王雅蕾 邱志强 陈璐 程润芬 王靖怡 孙保存

王雅蕾, 邱志强, 陈璐, 程润芬, 王靖怡, 孙保存. SVEP1 PKHD1 P53在原发性肝癌组织中的表达及其临床意义[J]. 中国肿瘤临床, 2019, 46(3): 105-110. doi: 10.3969/j.issn.1000-8179.2019.03.163
引用本文: 王雅蕾, 邱志强, 陈璐, 程润芬, 王靖怡, 孙保存. SVEP1 PKHD1 P53在原发性肝癌组织中的表达及其临床意义[J]. 中国肿瘤临床, 2019, 46(3): 105-110. doi: 10.3969/j.issn.1000-8179.2019.03.163
Wang Yalei, Qiu Zhiqiang, Chen Lu, Cheng Runfen, Wang Jingyi, Sun Baocun. SVEP1, PKHD1, and P53 expression in primary liver cancer and its clinical significance[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2019, 46(3): 105-110. doi: 10.3969/j.issn.1000-8179.2019.03.163
Citation: Wang Yalei, Qiu Zhiqiang, Chen Lu, Cheng Runfen, Wang Jingyi, Sun Baocun. SVEP1, PKHD1, and P53 expression in primary liver cancer and its clinical significance[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2019, 46(3): 105-110. doi: 10.3969/j.issn.1000-8179.2019.03.163

SVEP1 PKHD1 P53在原发性肝癌组织中的表达及其临床意义

doi: 10.3969/j.issn.1000-8179.2019.03.163
基金项目: 

受国家自然科学基金 81402420

天津市自然科学基金 15JCQNJC12400

天津市卫生局科学基金 16KG125

天津市教委科学基金 2017KJ202

详细信息
    作者简介:

    王雅蕾专业方向为肿瘤血管生成、肿瘤复发转移研究。E-mail:wangyl1022@163.com

    通讯作者:

    孙保存, sunbaocun2014@163.com

SVEP1, PKHD1, and P53 expression in primary liver cancer and its clinical significance

Funds: 

the National Natural Science Foundation of China 81402420

Tianjin Natural Science Foundation 15JCQNJC12400

Tianjin Municipal Health Bureau Grant 16KG125

Tianjin Education Commission Science Foundation 2017KJ202

More Information
  • 摘要:   目的  使用免疫组化法检测SVEP1、PKHD1与P53在原发性肝癌组织中的表达, 结合临床病理因素分析其预测肝癌患者术后复发情况的临床意义。  方法  回顾性分析2013年1月至2014年1月于天津医科大学肿瘤医院行手术切除且随访资料完整的103例原发性肝癌患者的临床资料。以ROC曲线为主要统计方法探究不同指标的免疫组化评分对于患者预后的预测效果。根据其临界值将患者分为高危组和低危组, 以无瘤生存期主要研究指标比较两组间的差异。  结果  患者中位年龄为55(21~88)岁, 中位AFP水平70.6(1.03~718 840.0)μg/L, 中位CA19-9水平22.89(0.6~1 000.0) kU/L, 中位肿瘤大小4.5(1.0~27.0) cm。通过免疫组化法检测SVEP1、PKHD1、P53在原发性肝癌中的表达情况, 表达水平使用免疫组化评分进行量化, 三个指标免疫组化评分的ROC曲线中AUC面积分别为0.861、0.829、0.716, 临界值分别为4、4、1分(P < 0.001)。SVEP1高危组(≤4分)与低危组(>4分)3年无瘤生存率分别为4.1%和51.7%;PKHD1高危组(≤4分)与低危组(>4分)3年无瘤生存率分别为5.3%和51.9%;P53高危组(>1分)与低危组(≤1分)3年无瘤生存率分别为6.3%和27.3%, 每个指标两组间差异均有统计学意义(P < 0.001, < 0.001, 0.003)。PKHD1与SVEP1联合应用时, 其ROC曲线的AUC面积为0.897(P < 0.001), 敏感性为76.5%, 特异性为94.4%。  结论  P53预测原发性肝癌复发的准确性不足, 不推荐首选使用。SVEP1、PKHD1预测原发性肝癌复发准确性较高, SVEP1特异性较高, PKHD1敏感性较强, 两者联用效果更佳。

     

  • 图  1  免疫组织化学染色(SP染色法×200, 标尺表示200 μm)

    图  2  SVEP1、PKHD1、P53免疫组化评分的ROC曲线分析

    A:SVEP1;B:PKHD1;C:P53

    图  3  SVEP1、PKHD1、P53免疫组化评分高危组与低危组的生存分析

    A:SVEP1;B:PKHD1;C:P53

    图  4  SVEP1、PKHD1免疫组化评分联合应用的ROC曲线分析

    表  1  103例原发性肝癌患者的基线水平分析

  • [1] 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
    [2] 原发性肝癌诊疗规范(2011年版)[J].临床肝胆病杂志.2011, (11):1141-1159.DOI: 10.3969/j.issn.1001-5256.2011.11.004
    [3] Forner A, Reig M, Bruix J.Hepatocellular carcinoma[J].Lancet, 2018, 391(10127):1301-1314. doi: 10.1016/S0140-6736(18)30010-2
    [4] Glait-Santar C, Benayahu D.Regulation of SVEP1 gene expression by 17β-estradiol and TNFα in pre-osteoblastic and mammary adenocarcinoma cells[J].J Steroid Biochem Mol Biol, 2012, 130(1-2):36-44. doi: 10.1016/j.jsbmb.2011.12.015
    [5] Ward CJ, Wu Y, Johnson RA, et al.Germline PKHD1 mutations are protective against colorectal cancer[J].Hum Genet, 2011, 129(3):345- 349. doi: 10.1007/s00439-011-0950-8
    [6] Koifman G, Shetzer Y, Eizenberger S, et al.A mutant p53-dependent embryonic stem cell gene signature is associated with augmented tumorigenesis of stem cells[J].Cancer Res, 2018, 78(20):5833-5847.
    [7] Sasaki Y, Yamada T, Tanaka H, et al.Risk of recurrence in a long-term follow-up after surgery in 417 patients with hepatitis B-or hepatitis C-related hepatocellular carcinoma[J].Ann Surg, 2006, 244(5):771-780. doi: 10.1097/01.sla.0000225126.56483.b3
    [8] Nishio T, Hatano E, Sakurai T, et al.Impact of Hepatic Steatosis on Disease-Free Survival in Patients with Non-B Non-C Hepatocellular Carcinoma Undergoing Hepatic Resection[J].Ann Surg Oncol, 2015, 22(7):2226-2234. doi: 10.1245/s10434-014-4181-9
    [9] Jing JS, Ye W, Jiang YK, et al.The Value of GPC3 and GP73 in Clinical Diagnosis of Hepatocellular Carcinoma[J].Clin Lab, 2017, 63(11):1903- 1909.
    [10] Liu T, Zu CH, Wang SS, et al.PIK3C2A mRNA functions as a miR-124 sponge to facilitate CD151 expression and enhance malignancy of hepatocellular carcinoma cells[J].Oncotarget, 2016, 7(28):43376- 43389.
    [11] Ke AW, Zhang PF, Shen YH, et al.Generation and characterization of a tetraspanin CD151/integrin α6β1-binding domain competitively binding monoclonal antibody for inhibition of tumor progression in HCC[J].Oncotarget, 2016, 7(5):6314-6322.
    [12] Liu JJ, Li Y, Chen WS, et al.Shp2 deletion in hepatocytes suppresses hepatocarcinogenesis driven by oncogenic β-Catenin, PIK3CA and MET [J].J Hepatol, 2018, 69(1):79-88. doi: 10.1016/j.jhep.2018.02.014
    [13] Bleau AM, Redrado M, Nistal-Villan E, et al.miR-146a targets c-met and abolishes colorectal cancer liver metastasis[J].Cancer Lett, 2018, 414: 257-267. doi: 10.1016/j.canlet.2017.11.008
    [14] Karpanen T, Padberg Y, van de Pavert SA, et al.An evolutionarily conserved role for polydom/svep1 during lymphatic vessel formation [J].Circ Res, 2017, 120(8):1263-1275. doi: 10.1161/CIRCRESAHA.116.308813
    [15] Morooka N, Futaki S, Sato-Nishiuchi R, et al.Polydom is an extracellular matrix protein involved in lymphatic vessel remodeling[J].Circ Res, 2017, 120(8):1276-1288. doi: 10.1161/CIRCRESAHA.116.308825
    [16] Nakada TA, Russell JA, Boyd JH, et al.Identification of a nonsynonymous polymorphism in the SVEP1 gene associated with altered clinical outcomes in septic shock[J].Crit Care Med, 2015, 43(1):101-108. doi: 10.1097/CCM.0000000000000604
    [17] Shur I, Zemer-Tov E, Socher R, et al.SVEP1 expression is regulated in estrogen-dependent manner[J].J Cell Physiol, 2007, 210(3):732-739. doi: 10.1002/(ISSN)1097-4652
    [18] Zhang YL, Xing X, Cai LB, et al.Integrin α9 Suppresses hepatocellular carcinoma metastasis by rho GTPase signaling[J].J Immunol Res, 2018, 2018:4602570.
    [19] Huhn S, Bevier M, Pardini B, et al.Colorectal cancer risk and patients' survival:influence of polymorphisms in genes somatically mutated in colorectal tumors[J].Cancer Causes Control, 2014, 25(6):759-769. doi: 10.1007/s10552-014-0379-1
    [20] Dhar D, Antonucci L, Nakagawa H, et al.Liver cancer initiation requires p53 inhibition by CD44-enhanced growth factor signaling[J].Cancer Cell, 2018, 33(6):1061-1077. doi: 10.1016/j.ccell.2018.05.003
    [21] Liu X, Li Y, Meng L, et al.Reducing protein regulator of cytokinesis 1 as a prospective therapy for hepatocellular carcinoma[J].Cell Death Dis, 2018, 9(5):534. doi: 10.1038/s41419-018-0555-4
    [22] Cao P, Yang A, Wang R, et al.Germline duplication of SNORA18L5 increases risk for HBV-related hepatocellular carcinoma by altering localization of ribosomal proteins and decreasing levels of p53[J]. Gastroenterology, 2018, 155(2):542-556. doi: 10.1053/j.gastro.2018.04.020
    [23] Zhu H, Wang J, Yin J, et al.Downregulation of PRAME suppresses proliferation and promotes apoptosis in hepatocellular carcinoma through the activation of P53 mediated pathway[J].Cell Physiol Biochem, 2018, 45(3):1121-1135. doi: 10.1159/000487353
  • 加载中
图(4) / 表(1)
计量
  • 文章访问数:  61
  • HTML全文浏览量:  3
  • PDF下载量:  7
  • 被引次数: 0
出版历程
  • 收稿日期:  2018-10-31
  • 修回日期:  2019-02-01
  • 刊出日期:  2019-02-15

目录

    /

    返回文章
    返回