A non-canonical SWI/SNF complex is a synthetic lethal target in cancers driven by BAF complex perturbation.
A non-canonical SWI/SNF complex is a synthetic lethal target in cancers driven by BAF complex perturbation.
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DOI:
10.1038/s41556-018-0221-1
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发表时间:
2018-12
影响因子:
21.3
通讯作者:
Kadoch C
中科院分区:
文献类型:
--
作者:
Michel BC;D'Avino AR;Cassel SH;Mashtalir N;McKenzie ZM;McBride MJ;Valencia AM;Zhou Q;Bocker M;Soares LMM;Pan J;Remillard DI;Lareau CA;Zullow HJ;Fortoul N;Gray NS;Bradner JE;Chan HM;Kadoch C
Mammalian SWI/SNF chromatin remodeling complexes exist in three distinct, final-form assemblies: canonical BAF (cBAF), PBAF, and a newly-characterized non-canonical complex, ncBAF. However, their complex-specific targeting on chromatin, functions and roles in disease remain largely undefined. Here, we comprehensively mapped complex assemblies on chromatin and found that ncBAF complexes uniquely localize to CTCF sites and promoters. We identified ncBAF subunits as synthetic lethal targets specific to synovial sarcoma (SS) and malignant rhabdoid tumor (MRT), which share in common cBAF complex (SMARCB1 subunit) perturbation. Chemical and biological depletion of the BRD9 subunit of ncBAF rapidly attenuates SS and MRT cell proliferation. Notably, in cBAF-perturbed cancers, ncBAF complexes maintain gene expression at retained CTCF-promoter sites, and function in a manner distinct from fusion oncoprotein-bound complexes. Taken together, these findings unmask the unique chromatin targeting and function of ncBAF complexes and present new cancer-specific therapeutic targets.
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DOI:
10.1093/bioinformatics/btu638
发表时间:
2015-01-15
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Anders S;Pyl PT;Huber W
通讯作者:
Huber W
影响因子:
48
作者:
Langmead, Ben;Salzberg, Steven L.
通讯作者:
Salzberg, Steven L.
影响因子:
30.8
作者:
Kadoch, Cigall;Hargreaves, Diana C.;Hodges, Courtney;Elias, Laura;Ho, Lena;Ranish, Jeff;Crabtree, Gerald R.
通讯作者:
Crabtree, Gerald R.
影响因子:
4.8
作者:
Kaeser, Matthias D.;Aslanian, Aaron;Emerson, Beverly M.
通讯作者:
Emerson, Beverly M.
影响因子:
64.8
作者:
Hark, AT;Schoenherr, CJ;Tilghman, SM
通讯作者:
Tilghman, SM