High expression of LEF1 correlates with poor prognosis in solid tumors, but not blood tumors: a meta-analysis

Biosci Rep. 2020 Sep 30;40(9):BSR20202520. doi: 10.1042/BSR20202520.

Abstract

Background: Previously published studies have indicated that lymphoid enhancer-binding factor 1 (LEF1) expression could be recognized as a valuable biomarker to evaluate clinical outcome for various types of malignant cancer, but the results remained controversial. Therefore, we conducted this meta-analysis to pool the published estimates and discuss the relationship of LEF1 expression with cancer prognosis.

Methods: Five electronic databases Pubmed, Web of Science, Embase, CNKI, and Wanfang were systematically searched for eligible literatures. Hazard ratios (HRs) and 95% confidence intervals (CIs) from the included studies were combined to estimate the effect of LEF1 expression on cancer patients' survival.

Results: Eleven original studies met the criteria and were enrolled for analysis. The results indicated that compared with patients in low LEF1 expression group, patients in high LEF1 expression group tended to have shorter overall survival (HR = 1.74, 95% CI: 1.06-2.86, P=0.029), especially for patients with solid tumors (HR = 2.39, 95% CI: 1.86-3.08, P=0.000).

Conclusions: Individual evidence about the prognostic value of LEF1 expression in human cancers was limited. Our meta-analysis supported the suggestion that elevated LEF1 expression could function as a promising biomarker to predict the clinical outcomes for malignant cancers, especially solid tumors. More high-quality clinical studies are warranted to highlight the prognostic value of LEF1 expression in human cancers.

Keywords: LEF1; cancer; meta-analysis; prognosis.

Publication types

  • Meta-Analysis

MeSH terms

  • Biomarkers, Tumor / metabolism*
  • Disease-Free Survival
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Lymphoid Enhancer-Binding Factor 1 / metabolism*
  • Neoplasm Recurrence, Local / epidemiology*
  • Neoplasm Recurrence, Local / genetics
  • Neoplasms / genetics
  • Neoplasms / mortality*
  • Neoplasms / pathology
  • Prognosis
  • Risk Assessment / methods

Substances

  • Biomarkers, Tumor
  • LEF1 protein, human
  • Lymphoid Enhancer-Binding Factor 1