Circulating high mobility group AT-hook 2 and pleomorphic adenoma gene 1 in blood of patients with oral squamous cell carcinoma

J Oral Pathol Med. 2017 Nov;46(10):998-1003. doi: 10.1111/jop.12609. Epub 2017 Jul 24.

Abstract

Background: High mobility group AT-hook 2 (HMGA2) and pleomorphic adenoma gene 1(PLAG1) have been demonstrated to be elevated in many malignant tumors. However, the aim of this study was to evaluate HMGA2 and PLAG1 levels in blood as a non-invasive biomarker for oral squamous cell carcinoma (OSCC) diagnosis.

Methods: qRT-PCR was performed to measure circulating HMGA2 and PLAG1 levels in OSCC patients (n=43) and matched cancer-free blood control group (n=21). Clinical data of all patients were recorded.

Results: Circulating HMGA2 and PLAG1 in the 43 OSCC patients was significantly higher than in control group (P<.001, P=.038, respectively). Furthermore, HMGA2 expression in OSCC patients with poor-moderate differentiation was increased compared with well-differentiated group. However, no significant differences in PLAG1 expression were detected when differentiation was considered. In addition, the receiver operating characteristic (ROC) curve analysis for circulating HMGA2 revealed an area under the ROC curve of 0.876 (95% confidence interval, 0.793-0.959; P<.001) with 65.1% sensitivity and 100% specificity in discriminating OSCC from controls at a cutoff value of 14.380, demonstrating significant diagnostic value for OSCC.

Conclusion: Circulating HMGA2 levels are increased in OSCC patients and may potentially serve as a significant index to evaluate OSCC diagnosis.

Keywords: biomarker; diagnosis; high mobility group A2; oral squamous cell carcinoma; pleomorphic adenoma gene 1.

MeSH terms

  • Biomarkers, Tumor / blood
  • Carcinoma, Squamous Cell / blood*
  • Carcinoma, Squamous Cell / diagnosis*
  • Cell Cycle Proteins / blood*
  • Female
  • HMGA2 Protein / blood*
  • Humans
  • Male
  • Middle Aged
  • Mouth Neoplasms / blood*
  • Mouth Neoplasms / diagnosis*
  • Transcription Factors / blood*
  • Tumor Suppressor Proteins / blood*

Substances

  • Biomarkers, Tumor
  • Cell Cycle Proteins
  • HMGA2 Protein
  • PLAGL1 protein, human
  • Transcription Factors
  • Tumor Suppressor Proteins