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• W2607363971 abstract "SEs are large regulatory elements enabling cell-type-specific gene regulation and the maintenance of cell identity. SEs regulate cancer cell proliferation and survival as well as cell identity through the transcriptional regulation of genes that confer oncogenic traits and lineage specificity. SEs integrate diverse oncogenic signaling pathways to effectively modulate gene expression. Oncogenic SEs are acquired de novo during cellular transformation, often by still undefined processes. Targeted inhibition of SE assembly and function hinders tumor viability and growth through selective abrogation of key transcriptional regulators. Transcriptional deregulation is one of the core tenets of cancer biology and is underpinned by alterations in both protein-coding genes and noncoding regulatory elements. Large regulatory elements, so-called super-enhancers (SEs), are central to the maintenance of cancer cell identity and promote oncogenic transcription to which cancer cells become highly addicted. Such dependence on SE-driven transcription for proliferation and survival offers an Achilles heel for the therapeutic targeting of cancer cells. Indeed, inhibition of the cellular machinery required for the assembly and maintenance of SEs dampens oncogenic transcription and inhibits tumor growth. In this article, we review the organization, function, and regulation of oncogenic SEs and their contribution to the cancer cell state. Transcriptional deregulation is one of the core tenets of cancer biology and is underpinned by alterations in both protein-coding genes and noncoding regulatory elements. Large regulatory elements, so-called super-enhancers (SEs), are central to the maintenance of cancer cell identity and promote oncogenic transcription to which cancer cells become highly addicted. Such dependence on SE-driven transcription for proliferation and survival offers an Achilles heel for the therapeutic targeting of cancer cells. Indeed, inhibition of the cellular machinery required for the assembly and maintenance of SEs dampens oncogenic transcription and inhibits tumor growth. In this article, we review the organization, function, and regulation of oncogenic SEs and their contribution to the cancer cell state." @default.
• W2607363971 created "2017-04-28" @default.
• W2607363971 creator A5002000126 @default.
• W2607363971 creator A5056006147 @default.
• W2607363971 date "2017-04-01" @default.
• W2607363971 modified "2023-10-05" @default.
• W2607363971 title "Super-Enhancer-Driven Transcriptional Dependencies in Cancer" @default.
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• W2607363971 doi "https://doi.org/10.1016/j.trecan.2017.03.006" @default.
• W2607363971 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5546010" @default.
• W2607363971 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28718439" @default.

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