Non-self glycan structures as possible modulators of cancer progression: would polysaccharides from Cryptococcus spp. impact this phenomenon?

Braz J Microbiol. 2023 Jun;54(2):907-919. doi: 10.1007/s42770-023-00936-0. Epub 2023 Feb 25.

Abstract

Invasive fungal infections (IFI) are responsible for a large number of annual deaths. Most cases are closely related to patients in a state of immunosuppression, as is the case of patients undergoing chemotherapy. Cancer patients are severely affected by the worrisome proportions that an IFI can take during cancer progression, especially in an already immunologically and metabolically impaired patient. There is scarce knowledge about strategies to mitigate cancer progression in these cases, beyond conventional treatment with antifungal drugs with a narrow therapeutic range. However, in recent years, ample evidence has surfaced describing the possible interferences that IFI may have both on the progression of pre-existing cancers and in the induction of newly transformed cells. The leading gambit for modulation of tumor progression comes from the ability of fungal virulence factors to modulate the host's immune system, since they are found in considerable concentrations in the tumor microenvironment during infection. In this context, cryptococcosis is of particular concern, since the main virulence factor of the pathogenic yeast is its polysaccharide capsule, which carries constituents with high immunomodulatory properties and cytotoxic potential. Therefore, we open a discussion on what has already been described regarding the progression of cryptococcosis in the context of cancer progression, and the possible implications that fungal glycan structures may take in both cancer development and progression.

Keywords: Cancer; Cryptococcosis; Epithelial-mesenchymal transition process; Glycobiology; Glycoconjugates; Immunomodulation; Invasive fungal infection; Metastasis.

Publication types

  • Review

MeSH terms

  • Antifungal Agents
  • Cryptococcosis* / microbiology
  • Cryptococcus neoformans*
  • Humans
  • Neoplasms*
  • Polysaccharides
  • Tumor Microenvironment
  • Virulence Factors

Substances

  • Polysaccharides
  • Antifungal Agents
  • Virulence Factors