Altered Glycan Expression on Breast Cancer Cells Facilitates Infection by T3 Seroptype Oncolytic Reovirus

Danahe Mohammed (First Author), Melanie Koehler (Co-Author), Andra C. Dumitru (Co-Author), Pavithra Aravamudhan (Co-Author), Danica M. Sutherland (Co-Author), Terence S. Dermody* (Co-Author), David Alsteens* (Last Author)

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Breast cancer is the most common cancer in women. Although current therapies have increased survival rates for some breast cancer types, other aggressive invasive breast cancers remain difficult to treat. As the onset of breast cancer is often associated with the appearance of extracellular markers, these could be used to better target therapeutic agents. Here, we demonstrated by nanobiophysical approaches that overexpression of α-sialylated glycans in breast cancer provides an opportunity to combat cancer cells with oncolytic reoviruses. Notably, a correlation between cellular glycan expression and the mechanical properties of reovirus attachment and infection is observed in a serotype-dependent manner. Furthermore, we enhance the infectivity of reoviruses in malignant cells by the coinjection of α-sialylated glycans. In conclusion, this study supports both the use of reoviruses as an oncolytic agent in nanomedicine and the role of α-sialylated glycans as adjuvants in oncolysis, offering new perspective in oncolytic cancer therapy.

Original languageEnglish
Pages (from-to)9720-9728
Number of pages9
JournalNano Letters
Volume21
Issue number22
DOIs
StatePublished - 24 Nov 2021
Externally publishedYes

Keywords

  • Atomic force microscopy
  • breast cancer cells
  • cell mechanics
  • reovirus
  • sialylated glycans

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