Comprehensive characterization and clinical relevance of the SWI/SNF copy number aberrations across human cancers
Abstract Background Alterations in genes encoding chromatin regulatory proteins are prevalent in cancers and may confer oncogenic properties and molecular changes linked to therapy resistance. However, the impact of copy number alterations (CNAs) of the SWItch/Sucrose NonFermentable (SWI/SNF) comple...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2021-10-01
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Series: | Hereditas |
Subjects: | |
Online Access: | https://doi.org/10.1186/s41065-021-00203-y |