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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.
Afiliação
  • Saldova R; NIBRT GlycoScience Group, National Institute for Bioprocessing Research and Training, Dublin, Ireland.
  • Haakensen VD; Department of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, Norway.
  • Rødland E; Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, Norway.
  • Walsh I; Bioprocessing Technology Institute, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
  • Stöckmann H; NIBRT GlycoScience Group, National Institute for Bioprocessing Research and Training, Dublin, Ireland.
  • Engebraaten O; Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, Norway.
  • Børresen-Dale AL; Department of Oncology, Oslo University Hospital, Norway.
  • Rudd PM; Department of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, Norway.
Mol Oncol ; 11(10): 1361-1379, 2017 10.
Article em En | MEDLINE | ID: mdl-28657165
ABSTRACT
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polissacarídeos / Neoplasias da Mama / Glicoproteínas Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polissacarídeos / Neoplasias da Mama / Glicoproteínas Idioma: En Ano de publicação: 2017 Tipo de documento: Article