Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/115276
Author(s): Albuquerque, APB
Balmaña, M
Mereiter, S
Pinto, F
Reis, CA
Beltrão, EIC
Title: Hypoxia and serum deprivation induces glycan alterations in triple negative breast cancer cells
Publisher: De Gruyter
Issue Date: 2018-06-27
Abstract: Triple negative breast cancer (TNBC) is a major global public health problem. The lack of targeted therapy and the elevated mortality evidence the need for better knowledge of the tumor biology. Hypoxia and aberrant glycosylation are associated with advanced stages of malignancy, tumor progression and treatment resistance. Importantly, serum deprivation regulates the invasive phenotype and favors TNBC cell survival. However, in TNBC, the role of hypoxia and serum deprivation in the regulation of glycosylation remains largely unknown. The effects of hypoxia and serum deprivation on the expression of glycosyltransferases and glycan profile were evaluated in the MDA-MB-231 cell line. We showed that the overexpression of HIF-1α was accompanied by acquisition of epithelial-mesenchimal transition features. Significant upregulation of fucosyl- and sialyltransferases involved in the synthesis of tumor-associated carbohydrate antigens was observed together with changes in fucosylation and sialylation detected by Aleuria aurantia lectin and Sambucus nigra agglutinin lectin blots. Bioinformatic analysis further indicated a mechanism by which HIF-1α can regulate ST3GAL6 expression and the relationship within the intrinsic characteristics of TNBC tumors. In conclusion, our results showed the involvement of hypoxia and serum deprivation in glycosylation profile regulation of TNBC cells triggering breast cancer aggressive features and suggesting glycosylation as a potential diagnostic and therapeutic target.
Subject: Cancer cell biology
Glycosylation
Glycosyltransferases
Hypoxia
Serum deprivation
Triple negative breast cancer
URI: http://hdl.handle.net/10216/115276
Series: Biological chemistry, vol. 399(7), p. 661-672
Document Type: Artigo em Revista Científica Internacional
Rights: embargoedAccess
Embargo End Date: 2019-06-27
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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