Prognostic value of microvessel density, matrix metalloproteinase-9 and p53 protein expression in esophageal cancer
Background : Worldwide, esophageal carcinoma is one of the most aggressive cancers. It is relatively common in many countries and characterized by poor prognosis and rapid clinical progression. Purpose : In this study, we aimed to evaluate the role of CD34, the marker of vascular endothelial cells,...
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Veröffentlicht in: | Journal of Egyptian National Cancer Institute 2004-12, Vol.16 (4), p.224-230 |
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Zusammenfassung: | Background : Worldwide, esophageal carcinoma is
one of the most aggressive cancers. It is relatively common
in many countries and characterized by poor prognosis
and rapid clinical progression.
Purpose : In this study, we aimed to evaluate the role
of CD34, the marker of vascular endothelial cells, MMP-
9 (matrix metalloproteinase type 9) and p53 in esophageal
carcinoma.
Materials and Methods : Forty-four archival tissue
specimens, 38 cases with esophageal carcinoma and six
cases with normal mucosa, were immunohistochemically
stained with monoclonal antibodies against CD34, MMP-
9 and p53. In addition, flow cytometric DNA analysis was
carried out for patients and controls.
Results : The results showed that the DNA content
was diploid in all normal esophageal mucosa, whereas
aneuploidy was detected in twenty cases (52.6%) out of
38. The thirty-eight cases showed positive expression of
CD34 antigen. The expression of MMP-9 was identified
mainly in the cytoplasm in most of cancer cells in 27
cases (71%) out of 38. On the other hand, 28 (73.7%) out
of 38 were positive for p53 expression. There was a
statistical significance for CD34, MMP-9 and p53 expressions
with tumor stage. Micro vessel density in patients
with highly positive staining for MMP-9 was higher than
in those with negative and weak staining for MMP-9 (p=
0.002).
Conclusion : Our data suggest that the expression of
CD34 and MMP-9 is associated with tumor progression
and possibly seems to be valuable markers and could offer
additional information about the aggressiveness and activity
of esophageal carcinoma lesions. |
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ISSN: | 1110-0362 1687-9996 |