Repository logo
 
Publication

Staining of E-Selectin Ligands on Paraffin-Embedded Sections of Tumor Tissue

dc.contributor.authorCarrascal, M
dc.contributor.authorTalina, C
dc.contributor.authorBorralho, P
dc.contributor.authorGonçalo Mineiro, A
dc.contributor.authorHenriques, AR
dc.contributor.authorPen, C
dc.contributor.authorMartins, M
dc.contributor.authorBraga, S
dc.contributor.authorSackstein, R
dc.contributor.authorVideira, P
dc.date.accessioned2018-08-07T10:11:33Z
dc.date.available2018-08-07T10:11:33Z
dc.date.issued2018-05-02
dc.description.abstractBACKGROUND: The E-selectin ligands expressed by cancer cells mediate adhesion of circulating cancer cells to endothelial cells, as well as within tissue microenvironments important for tumor progression and metastasis. The identification of E-selectin ligands within cancer tissue could yield new biomarkers for patient stratification and aid in identifying novel therapeutic targets. The determinants of selectin ligands consist of sialylated tetrasaccharides, the sialyl Lewis X and A (sLeX and sLeA), displayed on protein or lipid scaffolds. Standardized procedures for immunohistochemistry make use of the antibodies against sLeX and/or sLeA. However, antibody binding does not define E-selectin binding activity. METHODS: In this study, we developed an immunohistochemical staining technique, using E-selectin-human Ig Fc chimera (E-Ig) to characterize the expression and localization of E-selectin binding sites on paraffin-embedded sections of different cancer tissue. RESULTS: E-Ig successfully stained cancer cells with high specificity. The E-Ig staining show high reactivity scores in colon and lung adenocarcinoma and moderate reactivity in triple negative breast cancer. Compared with reactivity of antibody against sLeX/A, the E-Ig staining presented higher specificity to cancer tissue with better defined borders and less background. CONCLUSIONS: The E-Ig staining technique allows the qualitative and semi-quantitative analysis of E-selectin binding activity on cancer cells. The development of accurate techniques for detection of selectin ligands may contribute to better diagnostic and better understanding of the molecular basis of tumor progression and metastasis.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBMC Cancer. 2018 May 2;18(1):495.pt_PT
dc.identifier.doi10.1186/s12885-018-4410-xpt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/3018
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherBioMed Centralpt_PT
dc.subjectCHLC ANPATpt_PT
dc.subjectBiomarkerspt_PT
dc.subjectE-Selectin/geneticspt_PT
dc.subjectE-Selectin/metabolismpt_PT
dc.subjectImmunohistochemistrypt_PT
dc.subjectLigands
dc.subjectNeoplasms/genetics
dc.subjectNeoplasms/metabolism
dc.subjectNeoplasms/pathology
dc.subjectParaffin Embedding
dc.titleStaining of E-Selectin Ligands on Paraffin-Embedded Sections of Tumor Tissuept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue1pt_PT
oaire.citation.startPage495pt_PT
oaire.citation.titleBMC Cancerpt_PT
oaire.citation.volume18pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
BMC Cancer 495.pdf
Size:
8.84 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description:

Collections