Extracellular LGALS3BP: a potential disease marker and actionable target for antibody–drug conjugate therapy in glioblastoma

Author:

Dufrusine Beatrice123ORCID,Capone Emily12,Ponziani Sara4,Lattanzio Rossano12,Lanuti Paola25,Giansanti Francesco4,De Laurenzi Vincenzo12,Iacobelli Stefano6,Ippoliti Rodolfo4,Mangiola Annunziato7,Trevisi Gianluca78ORCID,Sala Gianluca12ORCID

Affiliation:

1. Department of Innovative Technologies in Medicine & Dentistry University “G. D'Annunzio” of Chieti‐Pescara Italy

2. Center for Advanced Studies and Technology (CAST) Chieti Italy

3. Department of Bioscience and Technology for Food Agriculture and Environment University of Teramo Italy

4. Department of Life, Health and Environmental Sciences University of L'Aquila Coppito Italy

5. Department of Medicine and Aging Sciences University “G. D'Annunzio” of Chieti‐Pescara Chieti Italy

6. MediaPharma s.r.l. Chieti Italy

7. Department of Neurosciences, Imaging and Clinical Sciences “G. D'Annunzio” University Chieti Italy

8. Neurosurgical Unit Santo Spirito Hospital Pescara Italy

Abstract

Glioblastoma multiforme (GBM) is a lethal disease characterized by an overall survival of about 1 year, making it one of the most aggressive tumours, with very limited therapeutic possibilities. Specific biomarkers for early diagnosis as well as innovative therapeutic strategies are urgently needed to improve the management of this deadly disease. In this work, we demonstrated that vesicular galectin‐3‐binding protein (LGALS3BP), a glycosylated protein overexpressed in a variety of human malignancies, is a potential GBM disease marker and can be efficiently targeted by a specific antibody–drug conjugate (ADC). Immunohistochemical analysis on patient tissues showed that LGALS3BP is highly expressed in GBM and, compared with healthy donors, the amount of vesicular but not total circulating protein is increased. Moreover, analysis of plasma‐derived extracellular vesicles from mice harbouring human GBM revealed that LGALS3BP can be used for liquid biopsy as a marker of disease. Finally, an ADC targeting LGALS3BP, named 1959‐sss/DM4, specifically accumulates in tumour tissue, producing a potent and dose‐dependent antitumor activity. In conclusion, our work provides evidence that vesicular LGALS3BP is a potential novel GBM diagnostic biomarker and therapeutic target deserving further preclinical and clinical validation.

Funder

Associazione Italiana per la Ricerca sul Cancro

Publisher

Wiley

Subject

Cancer Research,Genetics,Molecular Medicine,General Medicine,Oncology

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