Wang Jin-Dao, Jin Ketao, Chen Xiao-Ying, Lv Jie-Qing, Ji Ke-Wei
Department of Gastrointestinal Surgery, Shaoxing People's Hospital, Shaoxing Hospital of Zhejiang University, Shaoxing City, Zhejiang Province, China.
Psychosomatic Second Division, Shaoxing 7th People's Hospital, Shaoxing City, Zhejiang Province, China.
Oncotarget. 2017 Mar 7;8(10):16704-16711. doi: 10.18632/oncotarget.14335.
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.
胰腺导管腺癌(PDAC)是癌症死亡的主要原因之一。尽管在理解PDAC的发病机制方面已取得进展,但结果仍然很差。本研究的目的是进行一项荟萃分析,以评估SMAD4缺失与PDAC临床病理意义之间的确切关联。在PubMed、科学网、谷歌学术和EMBASE中检索相关出版物。数据由两名审阅者独立提取和评估。进行汇总数据分析,计算并总结比值比或风险比及其相应的置信区间。纳入12篇相关文章进行详细的全面审查和荟萃分析。与非恶性胰腺组织相比,PDAC中SMAD4蛋白缺失的频率显著增加,比值比为0.05,95%置信区间为0.01-0.23,p<0.0001。SMAD4缺失与PDAC患者的总体生存不良显著相关,风险比为0.61,95%置信区间为0.38-0.99,p=0.05。SMAD4缺失与PDAC的大小、分级和淋巴结转移无关。总之,SMAD4是PDAC诊断的生物标志物。SMAD4缺失与PDAC患者的预后不良显著相关。