Amplification of the EGFR and CCND1 are coordinated and play important roles in the progression of oral squamous cell carcinomas

Huei Tzu Chien, Sou De Cheng, Chun Ta Liao, Hung Ming Wang, Shiang Fu Huang*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

25 Scopus citations


Oral squamous cell carcinoma (OSCC) is a common cancer in Taiwan and worldwide. To provide some clues for clinical management of OSCC, 72 advanced-stage OSCCs were analyzed using two microarray platforms (26 cases with Affymetrix 500 K and 46 cases with Affymetrix SNP 6.0). Genomic identification of significant targets in cancer analyses were used to identify significant copy number alterations (CNAs) using a q-value cutoff of 0.25. Among the several significant regions, 12 CNAs were common between these two platforms. Two gain regions contained the well-known oncogenes EGFR (7p11.2) and CCND1 (11q13.3) and several known cancer suppressor genes, such as FHIT (3p14.2–p12.1), FAT1 (4q35.1), CDKN2A (9p21.3), and ATM (11q22.3–q24.3), reside within the 10 deletion regions. Copy number gains of EGFR and CCND1 were further confirmed by fluorescence in situ hybridization and TaqMan CN assay, respectively, in 257 OSCC cases. Our results indicate that EGFR and CCND1 CNAs are significantly associated with clinical stage, tumor differentiation, and lymph node metastasis. Furthermore, EGFR and CCND1 CNAs have an additive effect on OSCC tumor progression. Thus, current genome-wide CNA analysis provides clues for future characterization of important oncogenes and tumor suppressor genes associated with the behaviors of the disease.

Original languageEnglish
Article number760
Issue number6
StatePublished - 06 2019

Bibliographical note

Publisher Copyright:
© 2019 by the authors. Licensee MDPI, Basel, Switzerland.


  • Amplification
  • CCND1
  • Copy number analysis
  • EGFR
  • Oral squamous cell carcinoma


Dive into the research topics of 'Amplification of the EGFR and CCND1 are coordinated and play important roles in the progression of oral squamous cell carcinomas'. Together they form a unique fingerprint.

Cite this