Prognostic significance of matrix metalloproteinase-2, cathepsin D, and tenascin-C expression in colorectal carcinoma
Matrix metalloproteinase-2 (MMP-2) and cathepsin D (CD) play a significant role in degrading the components of basement membrane and extracellular matrix (ECM), whereas tenascin-C (TN-C) is a glycoprotein of the ECM related to cell adhesion and detachment. These proteins have been implicated in tumo...
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Veröffentlicht in: | Pathology, research and practice research and practice, 2004-01, Vol.200 (5), p.379-387 |
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Sprache: | eng |
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Zusammenfassung: | Matrix metalloproteinase-2 (MMP-2) and cathepsin D (CD) play a significant role in degrading the components of basement membrane and extracellular matrix (ECM), whereas tenascin-C (TN-C) is a glycoprotein of the ECM related to cell adhesion and detachment. These proteins have been implicated in tumor invasion and metastasis. Therefore, we aimed at investigating the prognostic significance of MMP-2, CD, and TN-C expressions in primary colorectal cancer.
Overall, 112 colorectal adenocarcinomas were included in the present study. MMP-2, CD, and TN-C expressions were evaluated by immunohistochemistry and correlated with clinicopathologic prognostic parameters and survival.
Diffuse stromal TN-C immunostaining was found to be significantly correlated with advanced stage and shorter survival time (
p=0.002 and 0.02, respectively). MMP-2 expression was found to correlate with lymph vessel invasion (
p=0.006) and stage (
p=0.03). CD expression was related to depth of invasion (
p=0.005). No significant relationship was found between survival and MMP-2 and CD expression (
p>0.05). In multivariate analysis, stage and vascular invasion were independent prognostic factors, whereas TN-C did not retain a clear independent relationship to survival (
p>0.05).
Our findings suggest that TN-C expression may be a potential prognostic marker in colorectal carcinoma. However, MMP-2 and CD do not appear to be significant indicators of survival. |
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ISSN: | 0344-0338 1618-0631 |
DOI: | 10.1016/j.prp.2004.02.012 |