The Ki67+ proliferation index correlates with increased cellular retinol-binding protein-1 and the coordinated loss of plakophilin-1 and desmoplakin during progression of cervical squamous lesions

Histopathology. 2007 Jul;51(1):87-97. doi: 10.1111/j.1365-2559.2007.02724.x.

Abstract

Aims: To investigate the modulation of cellular retinol-binding protein (CRBP)-1 and the desmosomal plaque proteins plakophilin (PKP)-1 and desmoplakin (DP) in correlation with the Ki67+ proliferation index (PI) during the progression of cervical squamous intraepithelial lesions (SIL) to squamous cell carcinoma (SCC).

Methods: Using in situ imaging by brightfield and confocal laser scanning microscopy, the expression of CRBP-1 protein and transcripts, PKP-1, DP and the Ki67 PI were analysed in 38 low-grade (L) SIL, 56 high-grade (H) SIL, 49 SCC, 30 control cervices and 10 human papillomavirus-positive condylomatous lesions.

Results: CRBP-1+ cells increased from 11.4% in the normal cervix to 80.3% in LSILs, 92.3% in HSILs and slightly decreased to 78.3% in invasive SCCs (P = 0.0001) in close association with the Ki67 PI (r =0.41; P < 0.0001). PKP-1+ and DP+ cells were correlated (0.32; P < 0.0001) and decreased from normal (81% versus 92.3%) to LSIL (53.1% versus 85.3%), to HSIL (46.4% versus 67.5%) and SCC (35.1% versus 35.9%). The Ki67+ PI was inversely correlated with DP (-0.20, P = 0.0014) and PKP-1 (-0.19, P = 0.015). Condylomata retained low CRBP-1 and high expression of PKP-1 and DP.

Conclusions: The gain of CRBP-1 and the loss of desmosomal proteins occur early in cervical carcinogenesis.

MeSH terms

  • Carcinoma, Squamous Cell / metabolism*
  • Carcinoma, Squamous Cell / pathology
  • Case-Control Studies
  • Cell Proliferation
  • Cell Transformation, Neoplastic / genetics
  • Cervix Uteri / metabolism
  • Cervix Uteri / pathology
  • Condylomata Acuminata / metabolism
  • Condylomata Acuminata / pathology
  • Desmoplakins / genetics
  • Desmoplakins / metabolism*
  • Disease Progression
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Ki-67 Antigen / genetics
  • Ki-67 Antigen / metabolism*
  • Plakophilins / genetics
  • Plakophilins / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Retinol-Binding Proteins / genetics
  • Retinol-Binding Proteins / metabolism*
  • Retinol-Binding Proteins, Cellular
  • Uterine Cervical Neoplasms / metabolism*
  • Uterine Cervical Neoplasms / pathology

Substances

  • Desmoplakins
  • Ki-67 Antigen
  • Plakophilins
  • RNA, Messenger
  • Retinol-Binding Proteins
  • Retinol-Binding Proteins, Cellular