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A therapeutic antibody targeting annexin-A1 inhibits cancer cell growth in vitro and in vivo

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posted on 2024-05-29, 10:48 authored by David Butcher, Hussein Al-Ali, Christopher Parris, Fiona Dempsey, Scott Chrichton, Chris Pepper, Charlene Fabian

In this study we conducted the first investigation to assess the efficacy of a novel therapeutic antibody developed to target annexin-A1 (ANXA1). ANXA1 is an immunomodulatory protein which has been shown to be overexpressed in, and promote the development and progression of, several cancer types. In particular, high ANXA1 expression levels correlate with poorer overall survival in pancreatic and triple-negative breast cancers, two cancers with considerable unmet clinical need. MDX-124 is a humanised IgG1 monoclonal antibody which specifically binds to ANXA1 disrupting its interaction with formyl peptide receptors 1 and 2 (FPR1/2). Here we show that MDX-124 significantly reduced proliferation (p < 0.013) in a dose-dependent manner across a panel of human cancer cell lines expressing ANXA1. The anti-proliferative effect of MDX-124 is instigated by arresting cell cycle progression with cancer cells accumulating in the G1 phase of the cell cycle. Furthermore, MDX-124 significantly inhibited tumour growth in both the 4T1-luc triple-negative breast and Pan02 pancreatic cancer syngeneic mouse models (p < 0.0001). These findings suggest ANXA1-targeted therapy is a viable and innovative approach to treat tumours which overexpress ANXA1.

History

Refereed

  • Yes

Volume

43

Page range

608–614

Publication title

Oncogene

ISSN

0950-9232

Publisher

Springer Nature

File version

  • Published version

Item sub-type

Article, Rapid Communication

Affiliated with

  • School of Life Sciences Outputs