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

  • Danahe Mohammed (Erstautor/-in)
  • , Melanie Koehler (Co-Autor/-in)
  • , Andra C. Dumitru (Co-Autor/-in)
  • , Pavithra Aravamudhan (Co-Autor/-in)
  • , Danica M. Sutherland (Co-Autor/-in)
  • , Terence S. Dermody* (Co-Autor/-in)
  • , David Alsteens* (Letztautor/-in)
  • *Korrespondierende/r Autor/-in für diese Arbeit
  • University of Louvain
  • University of Pittsburgh School of Medicine
  • UPMC Children's Hospital of Pittsburgh
  • Walloon ExceLlence Research Institute

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

9 Zitate (Scopus)

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.

OriginalspracheEnglisch
Seiten (von - bis)9720-9728
Seitenumfang9
FachzeitschriftNano Letters
Jahrgang21
Ausgabenummer22
DOIs
PublikationsstatusVeröffentlicht - 24 Nov. 2021
Extern publiziertJa

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