E2/E6 ratio and L1 immunoreactivity as biomarkers to determine HPV16-positive high-grade squamous intraepithelial lesions (CIN2 and 3) and cervical squamous cell carcinoma

J Gynecol Oncol. 2018 May;29(3):e38. doi: 10.3802/jgo.2018.29.e38. Epub 2018 Feb 1.

Abstract

Objective: Human papillomavirus (HPV) 16 is the most carcinogenic HPV genotype. We investigated if HPV16 L1 capsid protein and E2/E6 ratio, evaluated by cervical cytology, may be used as biomarkers of ≥cervical intraepithelial neoplasia (CIN) 2 lesions.

Methods: Cervical specimens were obtained from 226 patients with HPV16 single infection. Using cytology specimen, L1 capsid protein and E2/E6 ratio were detected and the results were compared with those of the conventional histologic analysis of cervical tissues (CIN1-3 and squamous cell carcinoma [SCC]) to evaluate the association.

Results: The L1 positivity of CIN2/3 was significantly lower than that of normal cervical tissue (p<0.001) and SCC demonstrated significantly lower L1 positivity than CIN1 (p<0.001). The mean E2/E6 ratios of specimens graded as SCC (0.356) and CIN2/3 (0.483) were significantly lower than those of specimens graded as CIN1 (0.786) and normal (0.793) (p<0.05). We observed that area under the receiver operating characteristic curve (AUC) for E2/E6 ratio (0.844; 95% confidence interval [CI]=0.793-0.895) was higher than that for L1 immunochemistry (0.636; 95% CI=0.562-0.711). A combination of E2/E6 ratio and L1 immunocytochemistry analyses showed the highest AUC (0.871; 95% CI=0.826-0.917) for the prediction of ≥CIN2 lesions.

Conclusion: To our knowledge, this is the first study to validate HPV L1 capsid protein expression and decreased HPV E2/E6 ratio as valuable predictive markers of ≥CIN2 cervical lesions. Cervical cytology may be analyzed longitudinally on an outpatient basis with noninvasive procedures as against invasive conventional histologic analysis.

Keywords: Cervical Intraepithelial Neoplasia; Human Papillomavirus Type 16 L1 Protein; Immunocytochemistry; Uterine Cervical Neoplasms; Viral Integration.

MeSH terms

  • Adult
  • Biomarkers, Tumor
  • Capsid Proteins / analysis*
  • Cervix Uteri / pathology
  • DNA-Binding Proteins / analysis*
  • Female
  • Human papillomavirus 16 / isolation & purification*
  • Humans
  • Immunohistochemistry
  • Middle Aged
  • Oncogene Proteins, Viral / analysis*
  • Repressor Proteins / analysis*
  • Squamous Intraepithelial Lesions of the Cervix / diagnosis*
  • Squamous Intraepithelial Lesions of the Cervix / pathology
  • Squamous Intraepithelial Lesions of the Cervix / virology
  • Uterine Cervical Neoplasms / diagnosis*
  • Uterine Cervical Neoplasms / pathology
  • Uterine Cervical Neoplasms / virology
  • Virus Integration

Substances

  • Biomarkers, Tumor
  • Capsid Proteins
  • DNA-Binding Proteins
  • E2 protein, Human papillomavirus type 16
  • E6 protein, Human papillomavirus type 16
  • HPV L1 protein, Human papillomavirus
  • Oncogene Proteins, Viral
  • Repressor Proteins