Publication: a1-acid glycoprotein (AGP): a possible carrier of
sialyl lewis X (slewis X) antigen in colorectal carcinoma
| dc.contributor.author | Croce, M.V. | es |
| dc.contributor.author | Sálice, V.C. | es |
| dc.contributor.author | Lacunza, E. | |
| dc.contributor.author | Segal-Eiras, A. | |
| dc.date.accessioned | 2011-06-30T11:59:48Z | |
| dc.date.available | 2011-06-30T11:59:48Z | |
| dc.date.issued | 2005 | |
| dc.description.abstract | Objectives: 1- to detect a1-acid glycoprotein (AGP) and sialyl Lewis x (sLex) in colorectal malignant, benign and normal samples; 2- to isolate AGP from colorectal cancer and 3- to study its immunoreactivity with an anti-sLex monoclonal antibody (MAb). Materials and methods: tissue and serum samples from 88 patients with colorectal cancer, 22 adenomas and 23 normal were included. Expression of AGP and sLex was studied by immunohistochemistry (IHC); isolation approach: AGP was precipitated with ammonium sulphate and immunoprecipitated with anti-AGP MAb. The immune complex formed was isolated by protein ASepharose CL-4B affinity chromatography and further eluted; fractions were analysed by SDS-PAGE and Western-blot. Statistical analysis was performed by means of Principal Component Analysis. Results: by Western blot employing anti-AGP MAb and sLex MAbs, isolated fractions from malignant samples showed a band at about 45kD. IHC revealed that AGP was expressed in 70% of colorectal carcinoma samples, 50% of benign and 35% of normals. SLex was detected in 31% of malignant samples, 41% of benign and in one normal sample. In malignant samples, AGP reaction comprised the whole specimen with a strong and homogeneous staining while normal and benign samples showed a restricted reaction. In cancer, sLex expression consisted in an intense reactivity in membrane, cellular debris and some cytoplasmic foci while normal and benign samples were occasionally stained. A statistically significant positive correlation was found between AGP and sLex expression. Serum AGP levels were measured by radial immunodiffusion and statistical comparative analysis with tissue expression did not show a correlation between both parameters. Conclusion: AGP may constitute a carrier of sLex in colorectal cancer. | es |
| dc.format | application/pdf | es |
| dc.format.extent | 7 | es |
| dc.identifier.issn | 0213-3911 | es |
| dc.identifier.uri | http://hdl.handle.net/10201/22441 | |
| dc.language | eng | es |
| dc.publisher | Murcia : F. Hernández | es |
| dc.relation.ispartof | Histology and histopathology | es |
| dc.rights | info:eu-repo/semantics/openAccess | es |
| dc.subject | Colorectal carcinoma | es |
| dc.subject | Metastasis | es |
| dc.subject.other | CDU::6 - Ciencias aplicadas::61 - Medicina | es |
| dc.title | a1-acid glycoprotein (AGP): a possible carrier of sialyl lewis X (slewis X) antigen in colorectal carcinoma | es |
| dc.type | info:eu-repo/semantics/article | es |
| dspace.entity.type | Publication | es |
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