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Defining molecular phenotypes of human papillomavirus-associated oropharyngeal squamous cell carcinoma: Validation of three-class hypothesis

  • Paul M. Weinberger
    ,
  • Ziwei Yu
    ,
  • Panteleimon Kountourakis
    ,
  • Clarence Sasaki
    ,
  • Bruce G. Haffty
    ,
  • Diane Kowalski
*Corresponding author for this work
  • ,
  • Shanghai Jiao Tong University
    ,
  • Yale University
    ,
  • Medical College of Georgia
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Objective: The purpose of this study was to determine if oropharyngeal squamous cell carcinoma (OSCC) classified into three groups based on human papillomavirus (HPV) 16 DNA presence and p16 expression display different protein expression patterns. Study Design: Cross-sectional study. Setting: A laboratory-based study of patients with OSCC treated at a tertiary care academic medical center. Subjects and Methods: Paraffin-embedded OSCC specimens from 77 patients classified into the three-class model (HPV negative, HPV inactive [HPV16+/p16-], and HPV active [HPV16+/p16+]) were queried for the expression of 14 tumor progression proteins using AQUA (HistoRx, New Haven CT). Protein expression between groups was assessed by analysis of variance. Global expression patterns were determined by unsupervised hierarchical clustering. Results: There were significant differences in expression of β-catenin (P = 0.009), epidermal growth factor receptor (P = 0.009), and vascular endothelial growth factor (P = 0.028) between groups. HPV-active tumors had overexpression of β-catenin. Hierarchical clustering showed HPV-negative and HPV-inactive tumors displayed association patterns distinct from HPV-active tumors. Conclusions: Tumors classified by HPV DNA presence and p16 expression have different molecular phenotypes. This is the first demonstration of overexpression of β-catenin (also found in HPV-caused cervical cancer) in HPV-active OSCC. HPV-active OSCC may share a similar ontogeny to HPV-caused cervical cancer.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 382-389.e1

Journal (Volume, Issue Number)

Otolaryngology - Head and Neck Surgery (Volume 141, Issue 3)

Publication milestones

  • Published - 09/2009

Publication status

Published - 09/2009

ISSN

0194-5998

Publication IDs

  • Scopus: 68949212920
  • PubMed: 19716018

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
3.50
SciVal
Author count
10
SciVal
citations
40
SciVal
Paper percentile
86
Fractional count
1
Fractional count
0.10
Fractional count
9
Fractional count
0.90
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
34
Mentions
1
Citation count
41

Funding Details

Sponsorships : Supported by Yale School of Medicine Institutional startup funds (AP), the Virginia Alden Wright Fund (CS), and a CORE Resident Research Grant #2006–26357 from the American Academy of Otolaryngology/Head and Neck Surgery (PMW). The funding sources had no involvement in the study design, data collection and analysis, interpretation of the data, writing of the manuscript, or decision to submit for publication.
FundersFunding number
American Academy of Otolaryngology-Head
-
Virginia Alden Wright Fund
2006–26357
Yale School of Medicine Institutional startup funds
-