Altered Glycosylation in Progression and Management of Bladder Cancer.
Magdalena WilczakMagdalena SurmanMałgorzata PrzybyłoPublished in: Molecules (Basel, Switzerland) (2023)
Bladder cancer (BC) is the 10th most common malignancy worldwide, with an estimated 573,000 new cases and 213,000 deaths in 2020. Available therapeutic approaches are still unable to reduce the incidence of BC metastasis and the high mortality rates of BC patients. Therefore, there is a need to deepen our understanding of the molecular mechanisms underlying BC progression to develop new diagnostic and therapeutic tools. One such mechanism is protein glycosylation. Numerous studies reported changes in glycan biosynthesis during neoplastic transformation, resulting in the appearance of the so-called tumor-associated carbohydrate antigens (TACAs) on the cell surface. TACAs affect a wide range of key biological processes, including tumor cell survival and proliferation, invasion and metastasis, induction of chronic inflammation, angiogenesis, immune evasion, and insensitivity to apoptosis. The purpose of this review is to summarize the current information on how altered glycosylation of bladder cancer cells promotes disease progression and to present the potential use of glycans for diagnostic and therapeutic purposes.
Keyphrases
- cell surface
- end stage renal disease
- oxidative stress
- newly diagnosed
- chronic kidney disease
- risk factors
- ejection fraction
- peritoneal dialysis
- dendritic cells
- prognostic factors
- spinal cord injury
- endothelial cells
- cell migration
- signaling pathway
- cell death
- endoplasmic reticulum stress
- cell cycle arrest
- type diabetes
- vascular endothelial growth factor
- healthcare
- cell proliferation
- small molecule
- risk assessment
- amino acid
- social media
- cell wall
- drug induced
- climate change