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MiR-200 family and cancer: From a meta-analysis view

期刊

MOLECULAR ASPECTS OF MEDICINE
卷 70, 期 -, 页码 57-71

出版社

ELSEVIER
DOI: 10.1016/j.mam.2019.09.005

关键词

miR-200; Cancer; meta-Analysis; Survival; Prognosis

资金

  1. China Scholarship Council
  2. National Natural Science Foundation of China [81772982]
  3. National Institutes of Health through the NIH Common Fund, Office of Strategic Coordination (OSC) [UH3TR00943-01]
  4. NCI [1R01 CA182905-01, 1R01CA222007-01A1]
  5. NIGMS [1R01GM122775-01]
  6. U54 grant [CA096297/CA096300]
  7. Team DOD grant [CA160445P1]
  8. Ladies Leukemia League grant
  9. Chronic Lymphocytic Leukemia Moonshot Flagship project
  10. Sister Institution Network Fund (SINF) 2017 grant
  11. Estate of C. G. Johnson Jr
  12. CDMRP [CA160445P1, 917395] Funding Source: Federal RePORTER

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The role of microRNAs (miRNAs) in cancer development was implicated as oncogene or tumor suppressor. One of the miRNA family, the miR-200 family, was mainly characterized as tumor suppressor. However, controversial results were reported. The associations between miR-200 family (consisting of five miRNAs: miR-141/200a/200b/200c/429) and cancer prognosis were inconsistent. Therefore, we conducted a meta-analysis by searching PubMed and Embase databases for studies assessing the association between the expression of miR-200 family and patients' survival of cancers. Hazard ratios (HRs) with 95% confidence intervals (CIs) were extracted from the studies and pooled HRs was determined to evaluate the association. This meta-analysis comprised 58 articles with 8107 cancer patients. The overall analysis showed that patients with higher expression of miR-200 family were associated with worse survival (HR = 1.206, 95% CI: 1.115-1.305, p < 0.001). In the stratified analysis, high level of miR-200b and miR-200c was associated with poor patients' survival. In the subgroup analysis, expression of miR-200a and miR-429 was associated with survival of breast cancer and liver cancer, respectively. Expression of miR-141 was found to be associated with favorable patients' survival in pancreatic cancer (HR = 0.275, 95% CI: 0.104-0.727, p = 0.009). In the subgroup analysis of sample type of miR-141, reverse associations with patients' survival were found from tissue (HR = 0.769, 95% CI: 0.597-0.990, p = 0.042) and blood (HR = 1.496, 95% CI: 1.183-1.893, p = 0.001). Our findings revealed that association between miR-200 family and prognosis of various cancer types was significant and the results needed specific interpretation.

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