Molecular and cytogenetic subgroups of oropharyngeal squamous cell carcinoma

Federica Perrone, Simona Suardi, Elisa Pastore, Paola Casieri, Marta Orsenigo, Stefano Caramuta, Gianpaolo Dagrada, Marco Losa, Lisa Licitra, Paolo Bossi, Samantha Staurengo, Maria Oggionni, Laura Locati, Giulio Cantu, Massimo Squadrelli, Antonino Carbone, Marco A. Pierotti, Silvana Pilotti

Research output: Contribution to journalArticle


Purpose: The aim of this study was to acquire further insights into the pathogenetic pathways of head and neck squamous cell carcinomas (HNSCC) that may be useful for identifying new biomarkers instrumental in developing more specific treatment approaches. Experimental Design: Cell cycle regulators and epidermal growth factor receptor (EGFR) and BRAF genes were analyzed in a series of 90 oropharyngeal SCCs of a cohort of surgically treated patients from a single institution, and the results were matched with the presence of high-risk human papillomavirus (HR-HPV) DNA and the TP53 status. Results: At least four distinct groups of tumors were identified sharing a common histology but displaying different molecular/cytogenetic patterns: (a) 19% were HPV-positive SCCs whose lack of alterations of the investigated genes could explain their particular natural history, which requires less aggressive treatment; (b) 37% were HPV-negative SCCs carrying TP53 mutations, which may be more effectively treated by drugs acting through p53-independent apoptosis; (c) 34% were HPV-negative SCCs carrying wild-type TP53 and loss of 9p21 (p16INK4a and p15INK4b) and/or cyclin D1 overexpression that justify treatment with DNA-damaging drugs followed by cell cycle inhibitors; and (d) 10% were HPV-negative lacking tumor suppressor genes and cell cycle alterations. The second, third, and fourth groups also showed an increased copy number of EGFR and chromosome 7 (43%) that might justify the additional or alternative use of EGFR inhibitors. Conclusions: Our findings suggest that assessing HPV, TP53, 9p21, and EGFR status may be crucial to finding more tailored and beneficial treatments for oropharyngeal SCCs.

Original languageEnglish
Pages (from-to)6643-6651
Number of pages9
JournalClinical Cancer Research
Issue number22
Publication statusPublished - Nov 15 2006


ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Perrone, F., Suardi, S., Pastore, E., Casieri, P., Orsenigo, M., Caramuta, S., Dagrada, G., Losa, M., Licitra, L., Bossi, P., Staurengo, S., Oggionni, M., Locati, L., Cantu, G., Squadrelli, M., Carbone, A., Pierotti, M. A., & Pilotti, S. (2006). Molecular and cytogenetic subgroups of oropharyngeal squamous cell carcinoma. Clinical Cancer Research, 12(22), 6643-6651.