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Identification of the cis­molecular neighbours of the immune checkpoint protein B7­H4 in the breast cancer cell­line SK­BR­3 by proteomic proximity labelling.
Rees, Johanna S; Cheung, Lawrence C C; Hamaia, Samir W; Davies, Gareth; Sandercock, Alan; Lilley, Kathryn S; Tigue, Natalie; Jackson, Antony P.
Affiliation
  • Rees JS; Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, United Kingdom.
  • Cheung LCC; Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, United Kingdom.
  • Hamaia SW; Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, United Kingdom.
  • Davies G; Oncology R&D, AstraZeneca, Cambridge, CB21 6GP, United Kingdom.
  • Sandercock A; Antibody Discovery and Protein Engineering, R&D, AstraZeneca, Cambridge, CB21 6GP, United Kingdom.
  • Lilley KS; Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, United Kingdom.
  • Tigue N; Antibody Discovery and Protein Engineering, R&D, AstraZeneca, Cambridge, CB21 6GP, United Kingdom.
  • Jackson AP; Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, United Kingdom.
Int J Oncol ; 57(1): 87-99, 2020 07.
Article in En | MEDLINE | ID: mdl-32319587
ABSTRACT
The immune checkpoint protein B7­H4 plays an important role in the positive as well as the negative regulation of immune T­cell responses. When expressed on cancer cells, B7­H4 inhibits T­cell activity, and numerous types of cancer cells use upregulation of B7­H4 as a survival strategy. Thus, B7­H4 is a potential target for anticancer drug therapy. Unfortunately, the cell biology of this molecule has yet to be fully elucidated. Even basic properties, such as the nature of B7­H4 interactors, are controversial. In particular, the cis­interactors of B7­H4 on cancer cell plasma membranes have not been investigated to date. The present study used a proteomic proximity­labelling assay to investigate the molecular neighbours of B7­H4 on the surface of the human breast cancer cells SK­BR­3. By comparison to a comprehensive proteome analysis of SK­BR­3 cells, the proximity method detected a relatively small number of low abundance plasma membrane proteins highly enriched for proteins known to modulate cell adhesion and immune recognition. It may be inferred that these molecules contribute to the immunosuppressive behaviour that is characteristic of B7­H4 on cancer cells.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Protein Interaction Mapping / V-Set Domain-Containing T-Cell Activation Inhibitor 1 Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans Language: En Journal: Int J Oncol Journal subject: NEOPLASIAS Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Protein Interaction Mapping / V-Set Domain-Containing T-Cell Activation Inhibitor 1 Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans Language: En Journal: Int J Oncol Journal subject: NEOPLASIAS Year: 2020 Document type: Article Affiliation country: