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Tamoxifen-resistant breast cancer cells exhibit reactivity with Wisteria floribunda agglutinin

Glycosylation is one of the most important post-translational modifications of cell surface proteins involved in the proliferation, metastasis and treatment resistance of cancer cells. However, little is known about the role of glycosylation as the mechanism of breast cancer cell resistance to endoc...

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Autores principales: Hlaing, May Thinzar, Horimoto, Yoshiya, Denda-Nagai, Kaori, Fujihira, Haruhiko, Noji, Miki, Kaji, Hiroyuki, Tomioka, Azusa, Ishizuka, Yumiko, Saeki, Harumi, Arakawa, Atsushi, Saito, Mitsue, Irimura, Tatsuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409572/
https://www.ncbi.nlm.nih.gov/pubmed/36006984
http://dx.doi.org/10.1371/journal.pone.0273513
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author Hlaing, May Thinzar
Horimoto, Yoshiya
Denda-Nagai, Kaori
Fujihira, Haruhiko
Noji, Miki
Kaji, Hiroyuki
Tomioka, Azusa
Ishizuka, Yumiko
Saeki, Harumi
Arakawa, Atsushi
Saito, Mitsue
Irimura, Tatsuro
author_facet Hlaing, May Thinzar
Horimoto, Yoshiya
Denda-Nagai, Kaori
Fujihira, Haruhiko
Noji, Miki
Kaji, Hiroyuki
Tomioka, Azusa
Ishizuka, Yumiko
Saeki, Harumi
Arakawa, Atsushi
Saito, Mitsue
Irimura, Tatsuro
author_sort Hlaing, May Thinzar
collection PubMed
description Glycosylation is one of the most important post-translational modifications of cell surface proteins involved in the proliferation, metastasis and treatment resistance of cancer cells. However, little is known about the role of glycosylation as the mechanism of breast cancer cell resistance to endocrine therapy. Herein, we aimed to identify the glycan profiles of tamoxifen-resistant human breast cancer cells, and their potential as predictive biomarkers for endocrine therapy. We established tamoxifen-resistant cells from estrogen receptor-positive human breast cancer cell lines, and their membrane-associated proteins were subjected to lectin microarray analysis. To confirm differential lectin binding to cellular glycoproteins, we performed lectin blotting analyses after electrophoretic separation of the glycoproteins. Mass spectrometry of the tryptic peptides of the lectin-bound glycoproteins was further conducted to identify glycoproteins binding to the above lectins. Finally, expression of the glycans that were recognized by a lectin was investigated using clinical samples from patients who received tamoxifen treatment after curative surgery. Lectin microarray analysis revealed that the membrane fractions of tamoxifen-resistant breast cancer cells showed increased binding to Wisteria floribunda agglutinin (WFA) compared to tamoxifen-sensitive cells. Glycoproteins seemed to be responsible for the differential WFA binding and the results of mass spectrometry revealed several membrane glycoproteins, such as CD166 and integrin beta-1, as candidates contributing to increased WFA binding. In clinical samples, strong WFA staining was more frequently observed in patients who had developed distant metastasis during tamoxifen treatment compared with non-relapsed patients. Therefore, glycans recognized by WFA are potentially useful as predictive markers to identify the tamoxifen-resistant and relapse-prone subset of estrogen receptor-positive breast cancer patients.
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spelling pubmed-94095722022-08-26 Tamoxifen-resistant breast cancer cells exhibit reactivity with Wisteria floribunda agglutinin Hlaing, May Thinzar Horimoto, Yoshiya Denda-Nagai, Kaori Fujihira, Haruhiko Noji, Miki Kaji, Hiroyuki Tomioka, Azusa Ishizuka, Yumiko Saeki, Harumi Arakawa, Atsushi Saito, Mitsue Irimura, Tatsuro PLoS One Research Article Glycosylation is one of the most important post-translational modifications of cell surface proteins involved in the proliferation, metastasis and treatment resistance of cancer cells. However, little is known about the role of glycosylation as the mechanism of breast cancer cell resistance to endocrine therapy. Herein, we aimed to identify the glycan profiles of tamoxifen-resistant human breast cancer cells, and their potential as predictive biomarkers for endocrine therapy. We established tamoxifen-resistant cells from estrogen receptor-positive human breast cancer cell lines, and their membrane-associated proteins were subjected to lectin microarray analysis. To confirm differential lectin binding to cellular glycoproteins, we performed lectin blotting analyses after electrophoretic separation of the glycoproteins. Mass spectrometry of the tryptic peptides of the lectin-bound glycoproteins was further conducted to identify glycoproteins binding to the above lectins. Finally, expression of the glycans that were recognized by a lectin was investigated using clinical samples from patients who received tamoxifen treatment after curative surgery. Lectin microarray analysis revealed that the membrane fractions of tamoxifen-resistant breast cancer cells showed increased binding to Wisteria floribunda agglutinin (WFA) compared to tamoxifen-sensitive cells. Glycoproteins seemed to be responsible for the differential WFA binding and the results of mass spectrometry revealed several membrane glycoproteins, such as CD166 and integrin beta-1, as candidates contributing to increased WFA binding. In clinical samples, strong WFA staining was more frequently observed in patients who had developed distant metastasis during tamoxifen treatment compared with non-relapsed patients. Therefore, glycans recognized by WFA are potentially useful as predictive markers to identify the tamoxifen-resistant and relapse-prone subset of estrogen receptor-positive breast cancer patients. Public Library of Science 2022-08-25 /pmc/articles/PMC9409572/ /pubmed/36006984 http://dx.doi.org/10.1371/journal.pone.0273513 Text en © 2022 Hlaing et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hlaing, May Thinzar
Horimoto, Yoshiya
Denda-Nagai, Kaori
Fujihira, Haruhiko
Noji, Miki
Kaji, Hiroyuki
Tomioka, Azusa
Ishizuka, Yumiko
Saeki, Harumi
Arakawa, Atsushi
Saito, Mitsue
Irimura, Tatsuro
Tamoxifen-resistant breast cancer cells exhibit reactivity with Wisteria floribunda agglutinin
title Tamoxifen-resistant breast cancer cells exhibit reactivity with Wisteria floribunda agglutinin
title_full Tamoxifen-resistant breast cancer cells exhibit reactivity with Wisteria floribunda agglutinin
title_fullStr Tamoxifen-resistant breast cancer cells exhibit reactivity with Wisteria floribunda agglutinin
title_full_unstemmed Tamoxifen-resistant breast cancer cells exhibit reactivity with Wisteria floribunda agglutinin
title_short Tamoxifen-resistant breast cancer cells exhibit reactivity with Wisteria floribunda agglutinin
title_sort tamoxifen-resistant breast cancer cells exhibit reactivity with wisteria floribunda agglutinin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409572/
https://www.ncbi.nlm.nih.gov/pubmed/36006984
http://dx.doi.org/10.1371/journal.pone.0273513
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