Clinicopathological significance of SMAD4 loss in pancreatic ductal adenocarcinomas: a systematic review and meta-analysis

被引:34
|
作者
Wang, Jin-Dao [1 ]
Jin, Ketao [1 ]
Chen, Xiao-Ying [2 ]
Lv, Jie-Qing [1 ]
Ji, Ke-Wei [1 ]
机构
[1] Zhejiang Univ, Shaoxing Hosp, Shaoxing Peoples Hosp, Dept Gastrointestinal Surg, Shaoxing City, Zhejiang, Peoples R China
[2] Shaoxing 7th Peoples Hosp, Psychosomat Div 2, Shaoxing City, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
PDAC; SMAD4; DPC4; diagnosis; prognosis; TGF-BETA; GROWTH-FACTOR; IMMUNOHISTOCHEMICAL EVALUATION; INTRAEPITHELIAL NEOPLASIA; DISEASE PROGRESSION; POOR-PROGNOSIS; CANCER CELLS; IN-VITRO; EXPRESSION; DPC4;
D O I
10.18632/oncotarget.14335
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) is one of the leading causes of cancer mortality. Although advances have been made in understanding the pathogenesis of PDAC, the outcome still remains poor. The aim of this study is to conduct a meta-analysis to evaluate the precise association between SMAD4 loss and clinicopathological significance in PDAC. A literature search was made in PubMed, Web of Science, Google scholar, and EMBASE for related publications. The data were extracted and assessed by two reviewers independently. Analysis of pooled data was performed, Odds Ratio or Hazard Ratio with corresponding confidence intervals was calculated and summarized. 12 relevant articles were included for full review in detail and meta-analysis. The frequency of SMAD4 protein loss was significantly increased in PDAC than in nonmalignant pancreatic tissue, Odd Ratio was 0.05 with 95% confidence interval 0.01-0.23, p<0.0001. SMAD4 loss was significantly associated with poor overall survival in patients with PDAC, Hazard Ratio was 0.61 with 95% confidence interval 0.38-0.99, p=0.05. SMAD4 loss was not correlated with the size, grades, and lymph node metastasis of PDAC. In conclusion, SMAD4 is a biomarker for the diagnosis of PDAC. SMAD4 loss is significantly related to poor prognosis in patients with PDAC.
引用
收藏
页码:16704 / 16711
页数:8
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