CDH1 promoter methylation in patients with cervical carcinoma: a systematic meta-analysis with trial sequential analysis

被引:11
作者
Liu, Guanyuan [1 ]
机构
[1] Capital Med Univ, Beijing Chaoyang Hosp, Dept Gynaecol & Obstet, 8 Workers Stadium South Rd, Beijing 100020, Peoples R China
关键词
CDH1; cervical cancer; CIN lesions; histology; promoter methylation; INVASION-SUPPRESSOR GENE; SQUAMOUS-CELL CARCINOMA; E-CADHERIN; DNA-METHYLATION; BREAST-CANCER; EXPRESSION; HYPERMETHYLATION; RELEVANCE; SERUM; LINES;
D O I
10.2217/fon-2017-0267
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: This study was performed to evaluate the correlation between CDH1 promoter methylation and cervical cancer. Methods: Trial sequential analysis was conducted to evaluate the required information size. Results: A total of 15 studies with 950 cervical cancers and 829 controls were identified. CDH1 promoter methylation was higher in cervical cancer than in cervical intraepithelial neoplasia lesions and normal cervical tissues. Subgroup analysis of ethnicity showed that CDH1 promoter methylation correlated with cervical cancer in Caucasians, but not in Asians. CDH1 promoter methylation was higher in cervical cancer cytology samples than in normal cytology samples. It was higher in squamous cell carcinoma than adenocarcinoma, but was not correlated with tumor stage, grade and overall survival. Conclusion: CDH1 promoter methylation may be correlated with cervical cancer carcinogenesis, especially for Caucasians. It was associated with histological subtypes. Trial sequential analysis showed that more studies are needed.
引用
收藏
页码:51 / 63
页数:13
相关论文
共 56 条
  • [1] Clinical Relevance of CDH1 and CDH13 DNA-Methylation in Serum of Cervical Cancer Patients
    Abudukadeer, Abida
    Bakry, Rania
    Goebel, Georg
    Mutz-Dehbalaie, Irene
    Widschwendter, Andreas
    Bonn, Guenther K.
    Fiegl, Heidi
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2012, 13 (07): : 8353 - 8363
  • [2] [Anonymous], REPORT STAT MED ANNO
  • [3] E-cadherin is a tumour invasion suppressor gene mutated in human lobular breast cancers
    Berx, G
    CletonJansen, AM
    Nollet, F
    deLeeuw, WJF
    vandeVijver, MJ
    Cornelisse, C
    vanRoy, F
    [J]. EMBO JOURNAL, 1995, 14 (24) : 6107 - 6115
  • [4] Trial sequential analysis reveals insufficient information size and potentially false positive results in many meta-analyses
    Brok, Jesper
    Thorlund, Kristian
    Gluud, Christian
    Wetterslev, Jorn
    [J]. JOURNAL OF CLINICAL EPIDEMIOLOGY, 2008, 61 (08) : 763 - 769
  • [5] TRANSCRIPTIONAL REGULATION OF THE HUMAN E-CADHERIN GENE IN HUMAN PROSTATE-CANCER CELL-LINES - CHARACTERIZATION OF THE HUMAN E-CADHERIN GENE PROMOTER
    BUSSEMAKERS, MJG
    GIROLDI, LA
    VANBOKHOVEN, A
    SCHALKEN, JA
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 203 (02) : 1284 - 1290
  • [6] E-cadherin-integrin crosstalk in cancer invasion and metastasis
    Canel, Marta
    Serrels, Alan
    Frame, Margaret C.
    Brunton, Valerie G.
    [J]. JOURNAL OF CELL SCIENCE, 2013, 126 (02) : 393 - 401
  • [7] E-cadherin expression is silenced by DNA methylation in cervical cancer cell lines and tumours
    Chen, CL
    Liu, SS
    Ip, SM
    Wong, LC
    Ng, TY
    Ngan, HYS
    [J]. EUROPEAN JOURNAL OF CANCER, 2003, 39 (04) : 517 - 523
  • [8] Promoter Hypermethylation in White Blood Cell DNA and Breast Cancer Risk
    Cho, Yoon Hee
    McCullough, Lauren E.
    Gammon, Marilie D.
    Wu, Hui-Chen
    Zhang, Yu-Jing
    Wang, Qiao
    Xu, Xinran
    Teitelbaum, Susan L.
    Neugut, Alfred I.
    Chen, Jia
    Santella, Regina M.
    [J]. JOURNAL OF CANCER, 2015, 6 (09): : 819 - 824
  • [9] Comment on: heterogeneity in meta-analysis should be expected and appropriately quantified
    Coory, Michael D.
    [J]. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2010, 39 (03) : 932 - 932
  • [10] Promoter methylation of TIMP3 and CDH1 predicts better outcome in head and neck squamous cell carcinoma treated by radiotherapy only
    De Schutter, H.
    Geeraerts, H.
    Verbeken, E.
    Nuyts, S.
    [J]. ONCOLOGY REPORTS, 2009, 21 (02) : 507 - 513