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Preferential Antibody and Drug Conjugate Targeting of the ADAM10 Metalloprotease in Tumours.
Yan, Hengkang; Vail, Mary E; Hii, Linda; Guo, Nancy; McMurrick, Paul J; Oliva, Karen; Wilkins, Simon; Saha, Nayanendu; Nikolov, Dimitar B; Lee, Fook-Thean; Scott, Andrew M; Janes, Peter W.
Afiliação
  • Yan H; Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, VIC 3084, Australia.
  • Vail ME; School of Cancer Medicine, La Trobe University, Heidelberg, VIC 3084, Australia.
  • Hii L; Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, VIC 3084, Australia.
  • Guo N; Monash Biomedicine Discovery Institute, Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC 3800, Australia.
  • McMurrick PJ; Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, VIC 3084, Australia.
  • Oliva K; Cabrini Monash University Department of Surgery, Cabrini Hospital, Malvern, VIC 3144, Australia.
  • Wilkins S; Cabrini Monash University Department of Surgery, Cabrini Hospital, Malvern, VIC 3144, Australia.
  • Saha N; Cabrini Monash University Department of Surgery, Cabrini Hospital, Malvern, VIC 3144, Australia.
  • Nikolov DB; Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC 3004, Australia.
  • Lee FT; Structural Biology Program, Memorial Sloan-Kettering Cancer Centre, New York, NY 10065, USA.
  • Scott AM; Structural Biology Program, Memorial Sloan-Kettering Cancer Centre, New York, NY 10065, USA.
  • Janes PW; Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, VIC 3084, Australia.
Cancers (Basel) ; 14(13)2022 Jun 28.
Article em En | MEDLINE | ID: mdl-35804938
ABSTRACT
ADAM10 is a transmembrane metalloprotease that sheds a variety of cell surface proteins, including receptors and ligands that regulate a range of developmental processes which re-emerge during tumour development. While ADAM10 is ubiquitously expressed, its activity is normally tightly regulated, but becomes deregulated in tumours. We previously reported the generation of a monoclonal antibody, 8C7, which preferentially recognises an active form of ADAM10 in human and mouse tumours. We now report our investigation of the mechanism of this specificity, and the preferential targeting of 8C7 to human tumour cell xenografts in mice. We also report the development of novel 8C7 antibody-drug conjugates that preferentially kill cells displaying the 8C7 epitope, and that can inhibit tumour growth in mice. This study provides the first demonstration that antibody-drug conjugates targeting an active conformer of ADAM10, a widely expressed transmembrane metalloprotease, enable tumour-selective targeting and inhibition.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article