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
- oxidative stress
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- endothelial cells
- signaling pathway
- prognostic factors
- risk factors
- peritoneal dialysis
- spinal cord injury
- cardiovascular events
- health information
- type diabetes
- vascular endothelial growth factor
- coronary artery disease
- cardiovascular disease
- immune response
- social media
- case control
- cell cycle arrest