Plasma LncRNA-ATB, a Potential Biomarker for Diagnosis of Patients with Coal Workers' Pneumoconiosis: A Case-Control Study

Int J Mol Sci. 2016 Aug 22;17(8):1367. doi: 10.3390/ijms17081367.

Abstract

LncRNA-ATB (lncRNA was activated by transforming growth factor-β) has been reported to be involved in specific physiological and pathological processes in human diseases, and could serve as biomarkers for cancers. However, the role of lncRNA-ATB in coal workers' pneumoconiosis (CWP) is still unknown. This study aimed to investigate the association between lncRNA-ATB and CWP. Quantitative real-time polymerase chain reaction was performed to detect plasma lncRNA-ATB expression in 137 CWP patients, 72 healthy coal miners and 168 healthy controls. LncRNA-ATB was significantly upregulated in CWP (p < 0.05). Compared with the healthy controls and healthy coal miners, the odds ratios (ORs) (95% confidence interval (CI)) for CWP were 2.57 (1.52-4.33) and 2.17 (1.04-4.53), respectively. LncRNA-ATB was positively associated with transforming growth factor-β1 (TGF-β1) (r = 0.30, p = 0.003) and negative correlated with vital capacity (VC) (r = -0.18, p = 0.033) and forced vital capacity (FVC) (r = -0.18, p = 0.046) in CWP patients. Compared with healthy controls, the area under the curve (AUC) was 0.84, resulting in a 71.17% sensitivity and 88.14% specificity. When compared with healthy coal miners, the AUC was 0.83, the sensitivity and specificity were 70.07% and 86.36%, respectively. LncRNA-ATB expression is commonly increased in CWP and significantly correlates with the TGF-β1 in CWP patients. Furthermore, elevated lncRNA-ATB was associated with CWP risk and may serve as a potential biomarker for CWP.

Keywords: biomarker; coal workers’ pneumoconiosis (CWP); epithelial-mesenchymal transition (EMT); lncRNA-ATB; long noncoding RNA.

MeSH terms

  • Anthracosis / blood*
  • Anthracosis / diagnosis*
  • Biomarkers / blood*
  • Case-Control Studies
  • Collagen Type I / blood
  • Collagen Type III / blood
  • Epithelial-Mesenchymal Transition / physiology
  • Humans
  • Matrix Metalloproteinase 2 / blood
  • Matrix Metalloproteinase 9 / blood
  • Middle Aged
  • RNA, Long Noncoding / blood*
  • Real-Time Polymerase Chain Reaction
  • Transforming Growth Factor beta / genetics

Substances

  • Biomarkers
  • Collagen Type I
  • Collagen Type III
  • RNA, Long Noncoding
  • Transforming Growth Factor beta
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9