Source:http://linkedlifedata.com/resource/pubmed/id/18395971
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2008-5-27
|
pubmed:abstractText |
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.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0304-3835
|
pubmed:author |
pubmed-author:BaranyFrancisF,
pubmed-author:ChenChin-TungCT,
pubmed-author:CullifordAlfred TAT4th,
pubmed-author:D'AlessioMatthewM,
pubmed-author:ForslundAnnA,
pubmed-author:GimbelMarkM,
pubmed-author:KhanSajid ASA,
pubmed-author:KuntzEleanorE,
pubmed-author:NashGarrett MGM,
pubmed-author:PatyPhilip BPB,
pubmed-author:WeiserMartin RMR,
pubmed-author:YamaguchiYukaY,
pubmed-author:ZengZhao-ShiZS
|
pubmed:issnType |
Print
|
pubmed:day |
8
|
pubmed:volume |
265
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
258-69
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:18395971-Cell Line, Tumor,
pubmed-meshheading:18395971-Colorectal Neoplasms,
pubmed-meshheading:18395971-Female,
pubmed-meshheading:18395971-Gene Amplification,
pubmed-meshheading:18395971-Gene Dosage,
pubmed-meshheading:18395971-Humans,
pubmed-meshheading:18395971-Liver Neoplasms,
pubmed-meshheading:18395971-Male,
pubmed-meshheading:18395971-Middle Aged,
pubmed-meshheading:18395971-Polymerase Chain Reaction,
pubmed-meshheading:18395971-Proto-Oncogene Proteins c-met
|
pubmed:year |
2008
|
pubmed:articleTitle |
c-Met gene amplification is associated with advanced stage colorectal cancer and liver metastases.
|
pubmed:affiliation |
Department of Surgery, Colorectal Service, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
|