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dc.contributor.authorNeeb, A
dc.contributor.authorFigueiredo, I
dc.contributor.authorGurel, B
dc.contributor.authorNava Rodrigues, D
dc.contributor.authorRekowski, J
dc.contributor.authorRiisnaes, R
dc.contributor.authorFerreira, A
dc.contributor.authorMiranda, S
dc.contributor.authorCrespo, M
dc.contributor.authorWestaby, D
dc.contributor.authorde Los Dolores Fenor de La Maza, M
dc.contributor.authorGuo, C
dc.contributor.authorCarmichael, J
dc.contributor.authorGrochot, R
dc.contributor.authorTunariu, N
dc.contributor.authorCato, ACB
dc.contributor.authorPlymate, SR
dc.contributor.authorde Bono, JS
dc.contributor.authorSharp, A
dc.coverage.spatialUnited States
dc.date.accessioned2023-11-23T10:53:18Z
dc.date.available2023-11-23T10:53:18Z
dc.date.issued2023-08-29
dc.identifier100245
dc.identifierS0023-6837(23)00188-5
dc.identifier.citationLaboratory Investigation, 2023, 103 (11), pp. 100245 -
dc.identifier.issn0023-6837
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6066
dc.identifier.eissn1530-0307
dc.identifier.eissn1530-0307
dc.identifier.doi10.1016/j.labinv.2023.100245
dc.identifier.doi10.1016/j.labinv.2023.100245
dc.description.abstractBCL-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.
dc.formatPrint-Electronic
dc.format.extent100245 -
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCIENCE INC
dc.relation.ispartofLaboratory Investigation
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBAG-1L
dc.subjectadvanced prostate cancer
dc.subjectandrogen receptor
dc.subjectbiomarker
dc.subjectimmunohistochemistry
dc.subjecttreatment resistance
dc.titleDevelopment and Validation of a New BAG-1L-Specific Antibody to Quantify BAG-1L Protein Expression in Advanced Prostate Cancer.
dc.typeJournal Article
dcterms.dateAccepted2023-08-18
dc.date.updated2023-11-23T10:52:46Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.labinv.2023.100245
rioxxterms.licenseref.startdate2023-08-29
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37652207
pubs.issue11
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-groupICR/Primary Group/ICR Divisions/Cancer Therapeutics/Cancer Biomarkers
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Cancer Biomarkers
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Translational Therapeutics
pubs.organisational-groupICR/Students
pubs.organisational-groupICR/Students/PhD and MPhil
pubs.organisational-groupICR/Students/PhD and MPhil/18/19 Starting Cohort
pubs.organisational-groupICR/Students/PhD and MPhil/20/21 Starting Cohort
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.labinv.2023.100245
pubs.volume103
icr.researchteamCancer Biomarkers
icr.researchteamTranslational Therapeutic
icr.researchteamPrCa Targeted Therapy
dc.contributor.icrauthorGurel, Bora
dc.contributor.icrauthorMiranda, Susana
dc.contributor.icrauthorCrespo, Mateus
dc.contributor.icrauthorWestaby, Daniel
dc.contributor.icrauthorDe Bono, Johann
dc.contributor.icrauthorSharp, Adam
icr.provenanceDeposited by Mr Arek Surman on 2023-11-23. Deposit type is initial. No. of files: 1. Files: 1-s2.0-S0023683723001885-main.pdf


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