Cyclin D1, p53, MIB1, intratumoral microvessel density, and human papillomavirus in advanced laryngeal carcinoma: association with nodal metastasis

Otolaryngol Head Neck Surg. 2004 Oct;131(4):509-13. doi: 10.1016/j.otohns.2004.03.029.

Abstract

Objective: We sought to study various parameters in laryngeal squamous cell carcinoma (LSCC) that might predict nodal metastasis.

Study design and setting: Sixty-four LSCCs were examined with respect to their histopathology and, using immunohistochemistry, their proliferative capacity (MIB1), p53 and cyclin D1 status, and intratumoral microvessel density. The presence of human papillomavirus was ascertained by the polymerase chain reaction.

Results: Histopathologically, most tumors had an infiltrating/mixed growth pattern and a diminished inflammatory reaction at the growing margin. In addition, 56% of the tumors were positive for MIB1, with 64% showing p53 overexpression; 70% were positive for cyclin D1; and 59% showed increased tumor microvessel density. Of 42 cases analyzed, 9.5% were positive for human papillomavirus 16.

Conclusions: Of the parameters studied, a diminished lymphocytic inflammatory response at the periphery (P < 0.05) and cyclin D1 overexpression (P < 0.001) correlated significantly with cervical nodal metastasis at presentation.

Significance: Cyclin D1 overexpression, easily assessed on biopsy samples, may thus help in optimizing therapy at the outset.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Carcinoma, Squamous Cell / blood supply
  • Carcinoma, Squamous Cell / pathology*
  • Carcinoma, Squamous Cell / virology
  • Cyclin D1 / analysis*
  • DNA-Binding Proteins / analysis*
  • Female
  • Humans
  • Immunohistochemistry
  • Laryngeal Neoplasms / blood supply
  • Laryngeal Neoplasms / chemistry
  • Laryngeal Neoplasms / pathology*
  • Laryngeal Neoplasms / virology
  • Lymphatic Metastasis / diagnosis*
  • Male
  • Middle Aged
  • Papillomaviridae / isolation & purification*
  • Polymerase Chain Reaction
  • Transcription Factors
  • Tumor Suppressor Protein p53 / analysis*

Substances

  • DNA-Binding Proteins
  • Transcription Factors
  • Tumor Suppressor Protein p53
  • Cyclin D1
  • HIVEP2 protein, human