Volume 9 Issue 2
Mar.  2018
Turn off MathJax
Article Contents
Li Hui, Wang Genshu, Zheng Jun, et al. Effect of high expression of Zwint on the proliferation of hepatoma cells and the prognosis of liver transplantation for hepatocellular carcinoma[J]. ORGAN TRANSPLANTATION, 2018, 9(2): 122-129. doi: 10.3969/j.issn.1674-7445.2018.02.006
Citation: Li Hui, Wang Genshu, Zheng Jun, et al. Effect of high expression of Zwint on the proliferation of hepatoma cells and the prognosis of liver transplantation for hepatocellular carcinoma[J]. ORGAN TRANSPLANTATION, 2018, 9(2): 122-129. doi: 10.3969/j.issn.1674-7445.2018.02.006

Effect of high expression of Zwint on the proliferation of hepatoma cells and the prognosis of liver transplantation for hepatocellular carcinoma

doi: 10.3969/j.issn.1674-7445.2018.02.006
More Information
  • Corresponding author: Wang Genshu, Email: wgsh168@163.com
  • Received Date: 2018-01-03
    Available Online: 2021-01-19
  • Publish Date: 2018-03-15
  •   Objective  To investigate the expression of zeste white 10 interactor (Zwint) in primary hepatocellular carcinoma (HCC) and its effect on the prognosis of liver transplantation for HCC.  Methods  HCC tissues, paracancerous tissues and clinical data of 50 liver transplant recipients for HCC were collected. The expression levels of Zwint messenger RNA (mRNA) and Zwint protein in 20 pairs of HCC tissues and paracancerous tissues of 20 liver transplant recipients for HCC were compared using real-time fluorescence quantitative polymerase chain reaction (PCR), Western Blot and immunohistochemistry (IHC). Two HCC cell lines HepG-2 which interfered with the expression of Zwint successfully were selected as si-Zwint-1 group and si-Zwint-2 group, and the blank control was taken as si-NC group. The cell proliferation and cell cycle of various groups were compared using cell counting kit (CCK) -8 experiment, flatcloning assay and cell cycle experiment. The consistency of the expression of Zwint and cyclin D1 in HCC tissues and cells was analyzed using Western Blot and IHC. The enrolled patients were divided into high expression group (22 cases) and low expression group (28 cases) based on the median of Zwint protein expression level, and the relationship of the expression level of Zwint protein and clinical characteristics, overall survival rate and disease free survival rate of liver transplant recipients for HCC was analyzed.  Results  The results of real-time fluorescence quantitative PCR showed that the expression level of Zwint mRNA in HCC tissues was higher than that of paracancerous tissues (P=0.03). The results of Western Blot and IHC showed that the expression level of Zwint protein in HCC tissues was higher than that of paracancerous tissues (both P < 0.05). After the Zwint gene of HCC cell line HepG-2 was interfered, CCK-8 and flatcloning assay showed that the cell proliferation potential was significantly weakened (all P < 0.01), and the cell cycle arrested at stage G1 (all P < 0.05). The expression level of Zwint protein was closely related to tumor diameter and tumor, node, metastasis (TNM) staging (all P < 0.05). The overall survival rate of liver transplant recipients for HCC in the high Zwint expression group was lower than that of the low expression group (P=0.02).  Conclusions  Zwint is highly expressed in HCC tissues, and it can promote the proliferation of HCC cells through regulating cell cycle. The expression level of Zwint is negatively correlated with the prognosis of liver transplantation for HCC.

     

  • loading
  • [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]
    MALUCCIO M, COVEY A. Recent progress in understanding, diagnosing, and treating hepatocellular carcinoma[J]. CA Cancer J Clin, 2012, 62(6): 394-399. DOI: 10.3322/caac.21161.
    [3]
    YANG JD, ROBERTS LR. Hepatocellular carcinoma: a global view[J]. Nat Rev Gastroenterol Hepatol, 2010, 7(8): 448-458. DOI: 10.1038/nrgastro.2010.100.
    [4]
    蔡燕, 黄俊琪.肝癌转移相关标志物的研究进展[J].实用医学杂志, 2017, 33(12): 2059-2061. DOI: 10.3969/j.issn.1006-5725.2017.12.045.

    CAI Y, HUANG JQ. Research on markers related to metastasis of hepatocellular carcinoma[J]. J Pract Med, 2017, 33(12): 2059-2061. DOI: 10.3969/j.issn.1006-5725.2017.12.045.
    [5]
    HWANG S, MOON DB, AHN CS, et al. Risk-based long-term screening for hepatocellular carcinoma recurrence after living donor liver transplantation[J]. Transplant Proc, 2013, 45(8): 3076-3084. DOI: 10.1016/j.transproceed.2013.08.068.
    [6]
    WOO SEO D, YEOP YOU S, CHUNG WJ, et al. Zwint-1 is required for spindle assembly checkpoint function and kinetochore-microtubule attachment during oocyte meiosis[J]. Sci Rep, 2015, 5:15431. DOI: 10.1038/srep15431.
    [7]
    XU Z, ZHOU Y, CAO Y, et al. Identification of candidate biomarkers and analysis of prognostic values in ovarian cancer by integrated bioinformatics analysis[J]. Med Oncol, 2016, 33(11): 130. doi: 10.1007/s12032-016-0840-y
    [8]
    CHEN L, LI Y, LIN CH, et al. Recoding RNA editing of AZIN1 predisposes to hepatocellular carcinoma[J]. Nat Med, 2013, 19(2): 209-216. DOI: 10.1038/nm.3043.
    [9]
    SARASWAT S, ROUT PK, KHARCHE SD, et al. Molecular expression of caprine estrogen receptor gene 1 in reproductive and non-reproductive tissues[J]. Reprod Domest Anim, 2016, 51(6): 1049-1054. DOI: 10.1111/rda.12774.
    [10]
    XIONG Y, HU B, WEI L, et al. Upregulated expression of polycomb protein Ring1 contributes to poor prognosis and accelerated proliferation in human hepatocellular carcinoma[J]. Tumour Biol, 2015, 36(12): 9579-9588. DOI: 10.1007/s13277-015-3721-7.
    [11]
    XING C, ZHOU W, DING S, et al. Reversing effect of ring finger protein 43 inhibition on malignant phenotypes of human hepatocellular carcinoma[J]. Mol Cancer Ther, 2013, 12(1): 94-103. DOI: 10.1158/1535-7163.MCT-12-0672.
    [12]
    WANG H, HU X, DING X, et al. Human Zwint-1 specifies localization of Zeste White 10 to kinetochores and is essential for mitotic checkpoint signaling[J].J Biol Chem, 2004, 279(52): 54590-54598. doi: 10.1074/jbc.M407588200
    [13]
    BARTKOVA J, HOREJSÍ Z, KOED K, et al. DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis[J]. Nature, 2005, 434(7035): 864-870. doi: 10.1038/nature03482
    [14]
    GORGOULIS VG, VASSILIOU LV, KARAKAIDOS P, et al. Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions[J]. Nature, 2005, 434(7035): 907-913. doi: 10.1038/nature03485
    [15]
    KOPS GJ, WEAVER BA, CLEVELAND DW. On the road to cancer: aneuploidy and the mitotic checkpoint[J]. Nat Rev Cancer, 2005, 5(10): 773-785. doi: 10.1038/nrc1714
    [16]
    BRENDLE A, BRANDT A, JOHANSSON R, et al. Single nucleotide polymorphisms in chromosomal instability genes and risk and clinical outcome of breast cancer: a Swedish prospective case-control study[J]. Eur J Cancer, 2009, 45(3): 435-442. DOI: 10.1016/j.ejca.2008.10.001.
    [17]
    ZHONG Z, YEOW WS, ZOU C, et al. Cyclin D1/cyclin-dependent kinase 4 interacts with filamin A and affects the migration and invasion potential of breast cancer cells[J]. Cancer Res, 2010, 70(5): 2105-2114. DOI: 10.1158/0008-5472.CAN-08-1108.
    [18]
    LI Z, QU L, LUO W, et al. Mig-6 is down-regulated in HCC and inhibits the proliferation of HCC cells via the P-ERK/Cyclin D1 pathway[J]. Exp Mol Pathol, 2017, 102(3): 492-499. DOI: 10.1016/j.yexmp.2017.05.004.
    [19]
    COCO MARTIN JM, BALKENENDE A, VERSCHOOR T, et al. Cyclin D1 overexpression enhances radiation-induced apoptosis and radiosensitivity in a breast tumor cell line[J]. Cancer Res, 1999, 59(5): 1134-1140. https://www.researchgate.net/profile/Francois_Lallemand/publication/13219816_Cyclin_D1_overexpression_enhances_radiation-induced_apoptosis_and_radiosensitivity_in_a_breast_tumor_cell_line/links/54e343d90cf2d618e19630af.pdf
    [20]
    LING L, WEI T, HE L, et al. Low-intensity pulsed ultrasound activates ERK1/2 and PI3K-Akt signalling pathways and promotes the proliferation of human amnion-derived mesenchymal stem cells[J]. Cell Prolif, 2017, 50(6): e12383. DOI: 10.1111/cpr.12383.
    [21]
    李文梅, 刘佳佳, 张印坡, 等.乳腺癌组织中周期素依赖性激酶10基因启动子甲基化状态检测的临床意义[J].转化医学杂志, 2017, 6(1): 20-21, 31. DOI: 10.3969/j.issn.2095-3097.2017.01.005

    LI WM, LIU JJ, ZHANG YP, et al. Clinical significance of the cyclin-dependent kinase 10 gene promoter methylation in breast cancer[J]. Translat Med J, 2017, 6(1): 20-21, 31. DOI: 10.3969/j.issn.2095-3097.2017.01.005.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(4)  / Tables(1)

    Article Metrics

    Article views (146) PDF downloads(9) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return