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Differential Expression of Blood Group Precursor Antigen in Human Breast Cancer Tissue

There is a pressing need for biomarkers for targeted immunotherapy against breast cancer (BCA), the leading cause of cancer death in women. Previously, a blood group precursor O-core epitope gp(Cl) was found to be highly expressed in breast circulating tumor cells (BCTCs) and BCA cell lines with can...

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Detalles Bibliográficos
Autores principales: Jiang, Yi, Wang, Denong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462418/
https://www.ncbi.nlm.nih.gov/pubmed/32879924
http://dx.doi.org/10.31487/j.ijcst.2020.01.04
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author Jiang, Yi
Wang, Denong
author_facet Jiang, Yi
Wang, Denong
author_sort Jiang, Yi
collection PubMed
description There is a pressing need for biomarkers for targeted immunotherapy against breast cancer (BCA), the leading cause of cancer death in women. Previously, a blood group precursor O-core epitope gp(Cl) was found to be highly expressed in breast circulating tumor cells (BCTCs) and BCA cell lines with cancer stem cell (BCSC) features. In this pilot study, the breast tissue distribution of gp(C1) was examined using tissue microarrays (TMAs). Notably, gp(C1) positive cells were detected in the major histological types of neoplastic breast tissues. Conversely, none of the breast tissues derived from subjects without BCA were gp(C1) positive. Thus, gp(C1) expression seems to be tumor-specific but not histological type-dependent, reflecting perhaps its characteristics as a conserved epitope of oncofetal blood group precursor antigens.
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spelling pubmed-74624182020-09-01 Differential Expression of Blood Group Precursor Antigen in Human Breast Cancer Tissue Jiang, Yi Wang, Denong Int J Cancer Sci Ther Article There is a pressing need for biomarkers for targeted immunotherapy against breast cancer (BCA), the leading cause of cancer death in women. Previously, a blood group precursor O-core epitope gp(Cl) was found to be highly expressed in breast circulating tumor cells (BCTCs) and BCA cell lines with cancer stem cell (BCSC) features. In this pilot study, the breast tissue distribution of gp(C1) was examined using tissue microarrays (TMAs). Notably, gp(C1) positive cells were detected in the major histological types of neoplastic breast tissues. Conversely, none of the breast tissues derived from subjects without BCA were gp(C1) positive. Thus, gp(C1) expression seems to be tumor-specific but not histological type-dependent, reflecting perhaps its characteristics as a conserved epitope of oncofetal blood group precursor antigens. 2020-08-14 2020 /pmc/articles/PMC7462418/ /pubmed/32879924 http://dx.doi.org/10.31487/j.ijcst.2020.01.04 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Jiang, Yi
Wang, Denong
Differential Expression of Blood Group Precursor Antigen in Human Breast Cancer Tissue
title Differential Expression of Blood Group Precursor Antigen in Human Breast Cancer Tissue
title_full Differential Expression of Blood Group Precursor Antigen in Human Breast Cancer Tissue
title_fullStr Differential Expression of Blood Group Precursor Antigen in Human Breast Cancer Tissue
title_full_unstemmed Differential Expression of Blood Group Precursor Antigen in Human Breast Cancer Tissue
title_short Differential Expression of Blood Group Precursor Antigen in Human Breast Cancer Tissue
title_sort differential expression of blood group precursor antigen in human breast cancer tissue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462418/
https://www.ncbi.nlm.nih.gov/pubmed/32879924
http://dx.doi.org/10.31487/j.ijcst.2020.01.04
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