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Heparan Sulfate Mimetics Differentially Affect Homologous Chemokines and Attenuate Cancer Development.

Chethan D ShanthamurthyShani Leviatan Ben-AryeNanjundaswamy Vijendra KumarSharon YehudaRon AmonRobert J WoodsVered Padler-KaravaniRagahvendra Kikkeri
Published in: Journal of medicinal chemistry (2021)
Achieving selective inhibition of chemokine activity by structurally well-defined heparan sulfate (HS) or HS mimetic molecules can provide important insights into their roles in individual physiological and pathological cellular processes. Here, we report a novel tailor-made HS mimetic, which furnishes an exclusive iduronic acid (IdoA) scaffold with different sulfation patterns and oligosaccharide chain lengths as potential ligands to target chemokines. Notably, highly sulfated-IdoA tetrasaccharide (I-45) exhibited strong binding to CCL2 chemokine thereby blocking CCL2/CCR2-mediated in vitro cancer cell invasion and metastasis. Taken together, IdoA-based HS mimetics offer an alternative HS substrate to generate selective and efficient inhibitors for chemokines and pave the way to a wide range of new therapeutic applications in cancer biology and immunology.
Keyphrases
  • papillary thyroid
  • squamous cell
  • dna damage
  • squamous cell carcinoma
  • liver fibrosis
  • liver injury
  • risk assessment
  • dendritic cells
  • regulatory t cells
  • structural basis