Development and Validation of a New BAG-1L-Specific Antibody to Quantify BAG-1L Protein Expression in Advanced Prostate Cancer.


Journal

Laboratory investigation; a journal of technical methods and pathology
ISSN: 1530-0307
Titre abrégé: Lab Invest
Pays: United States
ID NLM: 0376617

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 28 03 2023
revised: 15 08 2023
accepted: 18 08 2023
medline: 20 11 2023
pubmed: 1 9 2023
entrez: 31 8 2023
Statut: ppublish

Résumé

BCL-2-associated athanogene-1L (BAG-1L) is a critical co-regulator that binds to and enhances the transactivation function of the androgen receptor, leading to prostate cancer development and progression. Studies investigating the clinical importance of BAG-1L protein expression in advanced prostate cancer have been limited by the paucity of antibodies that specifically recognize the long isoform. In this study, we developed and validated a new BAG-1L-specific antibody using multiple orthogonal methods across several cell lines with and without genomic manipulation of BAG-1L and all BAG-1 isoforms. Following this, we performed exploratory immunohistochemistry to determine BAG-1L protein expression in normal human, matched castration-sensitive prostate cancer (CSPC) and castration-resistant prostate cancer (CRPC), unmatched primary and metastatic CRPC, and early breast cancer tissues. We demonstrated higher BAG-1L protein expression in CRPC metastases than in unmatched, untreated, castration-sensitive prostatectomies from men who remained recurrence-free for 5 years. In contrast, BAG-1L protein expression did not change between matched, same patient, CSPC and CRPC biopsies, suggesting that BAG-1L protein expression may be associated with more aggressive biology and the development of castration resistance. Finally, in a cohort of patients who universally developed CRPC, there was no association between BAG-1L protein expression at diagnosis and time to CRPC or overall survival, and no association between BAG-1L protein expression at CRPC biopsy and clinical outcome from androgen receptor targeting therapies or docetaxel chemotherapy. The limitations of this study include the requirement to validate the reproducibility of the assay developed, the potential influence of pre-analytical factors, timing of CRPC biopsies, relatively small patient numbers, and heterogenous therapies on BAG-1L protein expression, and the clinical outcome analyses performed. We describe a new BAG-1L-specific antibody that the research community can further develop to elucidate the biological and clinical significance of BAG-1L protein expression in malignant and nonmalignant diseases.

Identifiants

pubmed: 37652207
pii: S0023-6837(23)00188-5
doi: 10.1016/j.labinv.2023.100245
pii:
doi:

Substances chimiques

BCL2-associated athanogene 1 protein 0
Receptors, Androgen 0
Transcription Factors 0
Antibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100245

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Antje Neeb (A)

Institute of Cancer Research, London, United Kingdom.

Ines Figueiredo (I)

Institute of Cancer Research, London, United Kingdom.

Bora Gurel (B)

Institute of Cancer Research, London, United Kingdom.

Daniel Nava Rodrigues (D)

Institute of Cancer Research, London, United Kingdom.

Jan Rekowski (J)

Institute of Cancer Research, London, United Kingdom.

Ruth Riisnaes (R)

Institute of Cancer Research, London, United Kingdom.

Ana Ferreira (A)

Institute of Cancer Research, London, United Kingdom.

Susana Miranda (S)

Institute of Cancer Research, London, United Kingdom.

Mateus Crespo (M)

Institute of Cancer Research, London, United Kingdom.

Daniel Westaby (D)

Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom.

Maria de Los Dolores Fenor de La Maza (M)

Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom.

Christina Guo (C)

Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom.

Juliet Carmichael (J)

Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom.

Rafael Grochot (R)

Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom.

Nina Tunariu (N)

Royal Marsden NHS Foundation Trust, London, United Kingdom.

Andrew C B Cato (ACB)

Karlsruhe Institute of Technology (KIT), Institute for Biological and Chemical Systems-Biological Information Processing (IBCS-BIP), Eggenstein-Leopoldshafen, Germany.

Stephen R Plymate (SR)

University of Washington, Seattle, Washington; Geriatrics Research, Education and Clinical Center, VAPSHCS, Seattle, Washington.

Johann S de Bono (JS)

Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom. Electronic address: johann.de-bono@icr.ac.uk.

Adam Sharp (A)

Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom. Electronic address: adam.sharp@icr.ac.uk.

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