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Serum N‐glycome alterations in breast cancer during multimodal treatment and follow‐up

Using our recently developed high‐throughput automated platform, N‐glycans from all serum glycoproteins from patients with breast cancer were analysed at diagnosis, after neoadjuvant chemotherapy, surgery, radiotherapy and up to 3 years after surgery. Surprisingly, alterations in the serum N‐glycome...

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Autores principales: Saldova, Radka, Haakensen, Vilde D., Rødland, Einar, Walsh, Ian, Stöckmann, Henning, Engebraaten, Olav, Børresen‐Dale, Anne‐Lise, Rudd, Pauline M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623820/
https://www.ncbi.nlm.nih.gov/pubmed/28657165
http://dx.doi.org/10.1002/1878-0261.12105
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author Saldova, Radka
Haakensen, Vilde D.
Rødland, Einar
Walsh, Ian
Stöckmann, Henning
Engebraaten, Olav
Børresen‐Dale, Anne‐Lise
Rudd, Pauline M.
author_facet Saldova, Radka
Haakensen, Vilde D.
Rødland, Einar
Walsh, Ian
Stöckmann, Henning
Engebraaten, Olav
Børresen‐Dale, Anne‐Lise
Rudd, Pauline M.
author_sort Saldova, Radka
collection PubMed
description Using our recently developed high‐throughput automated platform, N‐glycans from all serum glycoproteins from patients with breast cancer were analysed at diagnosis, after neoadjuvant chemotherapy, surgery, radiotherapy and up to 3 years after surgery. Surprisingly, alterations in the serum N‐glycome after chemotherapy were pro‐inflammatory with an increase in glycan structures associated with cancer. Surgery, on the other hand, induced anti‐inflammatory changes in the serum N‐glycome, towards a noncancerous phenotype. At the time of first follow‐up, glycosylation in patients with affected lymph nodes changed towards a malignant phenotype. C‐reactive protein showed a different pattern, increasing after first line of neoadjuvant chemotherapy, then decreasing throughout treatment until 1 year after surgery. This may reflect a switch from acute to chronic inflammation, where chronic inflammation is reflected in the serum after the acute phase response subsides. In conclusion, we here present the first time‐course serum N‐glycome profiling of patients with breast cancer during and after treatment. We identify significant glycosylation changes with chemotherapy, surgery and follow‐up, reflecting the host response to therapy and tumour removal.
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spelling pubmed-56238202017-10-04 Serum N‐glycome alterations in breast cancer during multimodal treatment and follow‐up Saldova, Radka Haakensen, Vilde D. Rødland, Einar Walsh, Ian Stöckmann, Henning Engebraaten, Olav Børresen‐Dale, Anne‐Lise Rudd, Pauline M. Mol Oncol Research Articles Using our recently developed high‐throughput automated platform, N‐glycans from all serum glycoproteins from patients with breast cancer were analysed at diagnosis, after neoadjuvant chemotherapy, surgery, radiotherapy and up to 3 years after surgery. Surprisingly, alterations in the serum N‐glycome after chemotherapy were pro‐inflammatory with an increase in glycan structures associated with cancer. Surgery, on the other hand, induced anti‐inflammatory changes in the serum N‐glycome, towards a noncancerous phenotype. At the time of first follow‐up, glycosylation in patients with affected lymph nodes changed towards a malignant phenotype. C‐reactive protein showed a different pattern, increasing after first line of neoadjuvant chemotherapy, then decreasing throughout treatment until 1 year after surgery. This may reflect a switch from acute to chronic inflammation, where chronic inflammation is reflected in the serum after the acute phase response subsides. In conclusion, we here present the first time‐course serum N‐glycome profiling of patients with breast cancer during and after treatment. We identify significant glycosylation changes with chemotherapy, surgery and follow‐up, reflecting the host response to therapy and tumour removal. John Wiley and Sons Inc. 2017-07-24 2017-10 /pmc/articles/PMC5623820/ /pubmed/28657165 http://dx.doi.org/10.1002/1878-0261.12105 Text en © 2017 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Saldova, Radka
Haakensen, Vilde D.
Rødland, Einar
Walsh, Ian
Stöckmann, Henning
Engebraaten, Olav
Børresen‐Dale, Anne‐Lise
Rudd, Pauline M.
Serum N‐glycome alterations in breast cancer during multimodal treatment and follow‐up
title Serum N‐glycome alterations in breast cancer during multimodal treatment and follow‐up
title_full Serum N‐glycome alterations in breast cancer during multimodal treatment and follow‐up
title_fullStr Serum N‐glycome alterations in breast cancer during multimodal treatment and follow‐up
title_full_unstemmed Serum N‐glycome alterations in breast cancer during multimodal treatment and follow‐up
title_short Serum N‐glycome alterations in breast cancer during multimodal treatment and follow‐up
title_sort serum n‐glycome alterations in breast cancer during multimodal treatment and follow‐up
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623820/
https://www.ncbi.nlm.nih.gov/pubmed/28657165
http://dx.doi.org/10.1002/1878-0261.12105
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