CCND1 messenger RNA expression is correlated with EGFR mutation status in lung cancer

Clin Lung Cancer. 2007 Sep;8(8):493-6. doi: 10.3816/CLC.2007.n.034.

Abstract

Background: Epidermal growth factor receptor (EGFR) stimulation markedly increases cyclin D1 protein expression. Recently, it has been reported that cyclin D1 expression was increased in EGFR mutant cell lines; however, the expression status of CCND1 in EGFR mutant lung cancer tissues has not been reported.

Patients and methods: We have investigated the CCND1 messenger RNA (mRNA) levels and other clinicopathologic data in 74 lung cancers. The CCND1 mRNA levels were quantified by real-time reverse-transcriptase polymerase chain reaction using LightCycler.

Results: The CCND1/GAPDH mRNA levels were significantly higher in adenocarcinoma (35.125 +/- 37.387) than in non-adenocarcinoma (15.2 +/- 24.699; P = .0158), and CCND1/GAPDH mRNA levels were not significantly different among smoking status, sex, or pathologic stage. The CCND1/GAPDH mRNA levels were significantly higher in lung cancer with EGFR mutation (39.713 +/- 41.265) than in lung cancer without EGFR mutation (21.805 +/- 29.152; P = .0338). CCND/GAPDH mRNA expression did not correlate with prognosis of lung cancer.

Conclusion: Using the LightCycler real-time reverse-transcriptase polymerase chain reaction assay, CCND1 gene expression might correlate with EGFR mutation in lung cancer. However, further studies are needed to confirm the impact of cyclin D1 for a molecular target of lung cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / genetics
  • Adult
  • Aged
  • Aged, 80 and over
  • Cyclin D
  • Cyclins / genetics*
  • ErbB Receptors / genetics*
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Glyceraldehyde-3-Phosphate Dehydrogenases / genetics
  • Humans
  • Lung Neoplasms / genetics*
  • Male
  • Middle Aged
  • Mutation
  • Prognosis
  • RNA, Messenger / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Cyclin D
  • Cyclins
  • RNA, Messenger
  • Glyceraldehyde-3-Phosphate Dehydrogenases
  • ErbB Receptors