c-Met gene amplification is associated with advanced stage colorectal cancer and liver metastases Academic Article uri icon


MeSH Major

  • Colorectal Neoplasms
  • Gene Amplification
  • Liver Neoplasms
  • Proto-Oncogene Proteins c-met


  • The c-Met proto-oncogene encodes a receptor tyrosine kinase (TK) that promotes invasive tumor growth and metastasis. Recent studies show that the presence of c-Met gene amplification is predictive for selective c-Met TK inhibitors in gastric cancer and lung cancer. In this study, we utilized a highly quantitative PCR/ligase detection reaction technique to quantify c-Met gene copy number in primary colorectal cancer (CRC) (N=247), liver metastases (N=147), and paired normal tissues. We identified no differences in c-Met gene copy number between normal colonic mucosa and liver tissue. However, mean c-Met gene copy number was significantly elevated in CRC compared with normal mucosa (P<0.001), and in liver metastases compared with normal liver (P<0.001). Furthermore, a significant increase in c-Met was seen in liver metastases compared with primary CRC (P<0.0001). c-Met gene amplification was observed in 2% (3/177) of localized cancers, 9% (6/70) of cancers with distant metastases (P<0.02), and 18% (25/147) of liver metastases (P<0.01). Among patients treated by liver resection, there was a trend toward poorer 3-year survival in association with c-Met gene amplification (P=0.07). Slight increases in c-Met copy number can be detected in localized CRCs, but gene amplification is largely restricted to Stage IV primary cancers and liver metastases. c-Met gene amplification is linked to metastatic progression, and is a viable target for a significant subset of advanced CRC.

publication date

  • July 8, 2008



  • Academic Article



  • eng

PubMed Central ID

  • PMC4367187

Digital Object Identifier (DOI)

  • 10.1016/j.canlet.2008.02.049

PubMed ID

  • 18395971

Additional Document Info

start page

  • 258

end page

  • 69


  • 265


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