Prognostic and clinicopathological value of Twist expression in breast cancer: A meta-analysis

PLoS One. 2017 Oct 9;12(10):e0186191. doi: 10.1371/journal.pone.0186191. eCollection 2017.

Abstract

Background: Despite initial indications that the transcription factor Twist could be used as a breast cancer prognostic marker, there still exists some controversy about its reliability. Thus, the aim of the present study was to assess the relationship between Twist expression and prognosis in breast carcinoma.

Materials and methods: We identified eligible studies that reported an association between Twist expression and breast cancer prognosis by searching the literature in PubMed, Embase, the Cochrane Library, and Web of Science databases, through June 5, 2017. Studies investigating Twist protein or mRNA expression as well as reporting survival data in breast cancer were included. The pooled hazard ratio (HR) and odds radio (OR) with a 95% confidence interval (95% CI) were used to estimate associations.

Results: A total of 2,671 patients from seven included studies were assessed, and the data indicated that increased Twist expression significantly correlated with poor overall survival (OS) (HR, 1.15; 95% CI, 1.00-1.33; P = 0.04) in breast cancer. In addition, we also observed a significant correlation of elevated Twist expression with larger tumor size (OR, 1.92; 95% CI, 1.31-2.81; P = 0.0009), lymph node involvement (OR, 3.81; 95% CI, 1.16-12.54; P = 0.03), higher nuclear grade (OR, 1.45; 95% CI, 1.06-2.00; P = 0.02), and positive human epidermal growth factor receptor 2 (HER2) status (OR, 1.49; 95% CI, 1.06-2.09; P = 0.02). However, no correlation between Twist expression and disease-free survival (DFS), age, estrogen receptor (ER) status, and progesterone receptor (PR) status was observed.

Conclusions: Our results demonstrate that Twist over-expression is a statistically significant indicator of OS in breast cancer. In addition, our meta-analysis shows that increased Twist expression is significantly associated with larger tumor size, lymph node involvement, higher nuclear grade, and positive HER2 status.

Publication types

  • Meta-Analysis

MeSH terms

  • Biomarkers, Tumor / biosynthesis
  • Biomarkers, Tumor / genetics*
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology
  • Disease-Free Survival
  • Estrogen Receptor alpha / genetics
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Lymphatic Metastasis / genetics
  • Prognosis*
  • Receptor, ErbB-2 / genetics
  • Receptors, Progesterone / genetics
  • Twist-Related Protein 1 / biosynthesis
  • Twist-Related Protein 1 / genetics*

Substances

  • Biomarkers, Tumor
  • Estrogen Receptor alpha
  • Receptors, Progesterone
  • Twist-Related Protein 1
  • ERBB2 protein, human
  • Receptor, ErbB-2

Grants and funding

This work was supported by the Program for Science &Technology Innovation teams in Universities of Henan Province (#181RTSTHN026), the innovation team of Henan University of Science and Technology (#2015XTD003) and Henan province’s Key Project of tackle key problems of science and technology (#172102310693). The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.