Target intelligence / Profile preview

BAF chromatin remodeling complex subunit BCL7B (BCL7B)

Target
BCL7B
Molecular classification
Other, Chromatin remodeling complex subunit
01

Overview

BAF chromatin remodeling complex subunit BCL7B (BCL7B) is a highly conserved protein and a member of the BCL7 protein family, including BCL7A and BCL7C[2][3]. It functions as an integral component of the BAF (SWI/SNF) chromatin remodeling complexes, which are responsible for modulating chromatin structure and regulating gene expression[1][2]. BCL7B lacks well-defined functional domains beyond a short conserved N-terminal region, but it plays a significant role in chromatin remodeling, cellular differentiation, maintenance of nuclear structure, regulation of apoptosis, and the Wnt signaling pathway[2][3]. Loss or downregulation of BCL7B is implicated in cancer, particularly lymphomas and sarcomas, and frequently associated with reduced tumor suppressor activity and poor prognosis[2][3]. Additionally, BCL7B is often deleted in Williams-Beuren syndrome, which may contribute both to developmental phenotypes and increased cancer risk in this disorder[2][3]. While BCL7B is not itself a classical therapeutic target such as a receptor or enzyme, its importance as a chromatin remodeling factor and tumor suppressor makes it potentially relevant as a disease biomarker and indirect cancer treatment target[3].

Other names
B-cell CLL/lymphoma 7 protein family member BSMARCJ2BCL tumor suppressor 7BB-cell CLL/lymphoma 7BBAF complex component BCL7BBCL7B_HUMAN
02

Biological functions

Chromatin remodelingRegulation of transcriptionCell cycle progressionApoptosisWnt signaling pathwayNuclear structure maintenanceStem cell differentiation
03

Disease associations

CancerLymphomaWilliams-Beuren syndromeDevelopmental disordersSarcoma
04

Safety considerations

Loss of BCL7B associated with increased malignancy/aggressiveness in cancerDeletion may contribute to Williams-Beuren syndrome phenotypes
05

Biomarkers

Potential biomarker for sarcoma prognosisPossibly involved in Williams-Beuren syndrome diagnosis

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