Bittersweet Sugars: How Unusual Glycan Structures May Connect Epithelial-to-Mesenchymal Transition and Multidrug Resistance in Cancer.
Leonardo Marques da FonsecaIsrael Diniz-LimaMarcos André Rodrigues da Costa SantosTatiany Nunes FranklimKelli Monteiro da CostaAriely Costa Dos SantosAlexandre MorrotDebora Decote-RicardoRaphael do Carmo ValenteCelio Geraldo Freire-de-LimaJhenifer Santos Dos ReisLeonardo Freire-de-LimaPublished in: Medicines (Basel, Switzerland) (2023)
Cancer cells are characterized by metabolic reprogramming, which enables their survival in of-ten inhospitable conditions. A very well-documented example that has gained attraction in re-cent years and is already considered a hallmark of transformed cells is the reprogramming of carbohydrate metabolism. Such a feature, in association with the differential expression of en-zymes involved in the biosynthesis of glycoconjugates, generically known as glycosyltransfer-ases, contributes to the expression of structurally atypical glycans when compared to those ex-pressed in healthy tissues. The latest studies have demonstrated that glycophenotypic alterations are capable of modulating multifactorial events essential for the development and/or progres-sion of the disease. Herein, we will address the importance of glycobiology in modern medi-cine, focusing on the ability of unusual/truncated O -linked glycans to modulate two complex and essential phenomena for cancer progression: the acquisition of the multidrug resistance (MDR) phenotype and the activation of molecular pathways associated with the epithelial-mesenchymal transition (EMT) process, an event deeply linked with cancer metastasis.
Keyphrases
- papillary thyroid
- epithelial mesenchymal transition
- squamous cell
- machine learning
- poor prognosis
- induced apoptosis
- signaling pathway
- squamous cell carcinoma
- high resolution
- lymph node metastasis
- young adults
- deep learning
- childhood cancer
- cell death
- cell proliferation
- long non coding rna
- single molecule
- free survival
- pi k akt