Abstract
c-Met, the receptor of hepatocyte growth factor is known to be responsible for the motility and mitogenesis of epithelial cells including cancer cells. To investigate the significance of c-Met expression in human colorectal cancer (CRC), total cellular protein, extracted from 130 CRCs were examined by Western blot analysis. The signal was quantitated by ChemiImager™ 4000 Low Light Imaging System. c-Met expression was analyzed as the ratio of tumor to matched normal tissue (T/N) and expressed as fold-increase. The cellular localization of c-Met was assessed by immunohistochemistry. The T/N fold increase of c-Met varied from 0.2 to 10.7 with a mean of 3.41 ± 0.23 (mean ± SE). 69% primary CRC showed overexpression (T/N >2.0) of c-Met. Significantly higher c-Met levels were found in CRC with blood vessel invasion (P = 0.04), and in advanced stage (P = 0.04). No relationship was noted between c-Met expression and age, tumor size, location, differentiation. C-Met immunoreactivity was observed in the membrane and cytoplasm of cancer cells. Positive staining of endothelial cells of blood vessels within normal submucosa and tumor was also evident. C-Met protein is expressed at levels significantly higher than adjacent mucosa in most primary adenocarcinomas of the colon. Our results support an important role for c-Met in human CRC progression and metastasis.
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Abbreviations
- BVI:
-
blood vessel invasion
- c-Met:
-
receptor of hepatocyte growth factor
- CRC:
-
colorectal cancer
- HGF:
-
hepatocyte growth factor
- LVI:
-
lymphatic vessel invasion
- MMPs:
-
matrix metalloproteinases
- SF:
-
scatter factor
- u-PA:
-
urokinase-type plasminogen activator
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Zeng, Z., Weiser, M.R., D’Alessio, M. et al. Immunoblot analysis of c-Met expression in human colorectal cancer: Overexpression is associated with advanced stage cancer. Clin Exp Metastasis 21, 409–417 (2004). https://doi.org/10.1007/s10585-005-1617-4
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DOI: https://doi.org/10.1007/s10585-005-1617-4