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Breast cancer anti-estrogen resistance protein 3 (BCAR3) (BCAR3)

Target
BCAR3
Molecular classification
Adaptor protein, SH2 domain-containing protein
01

Overview

Breast cancer anti-estrogen resistance protein 3 (BCAR3), also known as SH2D3B or NSP2, is a scaffold protein that plays a critical role in mediating resistance to anti-estrogen therapies, such as tamoxifen, in breast cancer (UniProt Q9Y2S2; PMID: 10467404). It functions primarily as an adaptor protein, utilizing its SH2 domain and GEF-like domain to interact with other signaling molecules like p130Cas (BCAR1) and PTPN13 (PMID: 21167771). These interactions activate downstream pathways involving Src, focal adhesion kinase (FAK), and Rho GTPases, which promote cell proliferation, survival, and increased motility (PMID: 25403711). Beyond its role in oncology, genetic variants in the BCAR3 gene have been strongly associated with Paget's disease of bone, suggesting a role in osteoclast function and bone remodeling (NCBI Gene 8412; PMID: 21167771). As a therapeutic target, BCAR3 is of interest for overcoming endocrine resistance in ER-positive breast cancers, though no specific small-molecule inhibitors are currently in clinical use. Targeting BCAR3 mRNA via antisense oligonucleotides or siRNA represents a potential strategy to downregulate its expression and restore drug sensitivity in resistant tumors.

Other names
SH2 domain-containing protein 3BSH2D3BNovel SH2-containing protein 2NSP2
02

Mechanism of action

Downregulation of BCAR3 expression via RNA interference or antisense oligonucleotides to inhibit downstream signaling pathways.

03

Biological functions

Signal transductionCell migrationCell adhesionRegulation of Rho GTPase activityEstrogen signaling modulation
04

Disease associations

CancerPaget's disease of bone
05

Safety considerations

Potential disruption of normal cell adhesionPotential impact on bone homeostasis
06

Interacting drugs

None currently approved
07

Biomarkers

BCAR3 mRNA expression levelBCAR3 protein expression level

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