High-Throughput Functional Genetic and Compound Screens Identify Targets for Senescence Induction in Cancer

Senescence is a proliferation arrest that can result from a variety of stresses. Cancer cells can also undergo senescence, but the stresses that provoke cancer cells to undergo senescence are unclear. Here, we use both functional genetic and compound screens in cancer cells harboring a reporter that...

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Vydané v:Cell reports (Cambridge) Ročník 21; číslo 3; s. 773 - 783
Hlavní autori: Wang, Liqin, Leite de Oliveira, Rodrigo, Wang, Cun, Fernandes Neto, João M., Mainardi, Sara, Evers, Bastiaan, Lieftink, Cor, Morris, Ben, Jochems, Fleur, Willemsen, Lisa, Beijersbergen, Roderick L., Bernards, René
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States Elsevier Inc 17.10.2017
Elsevier
Predmet:
aurora kinase
Aurora Kinases - antagonists & inhibitors
Aurora Kinases - metabolism
Cell Line, Tumor
Cellular Senescence - drug effects
Cellular Senescence - genetics
compound screen
CRISPR-Cas Systems - genetics
Down-Regulation - genetics
Gene Knockout Techniques
Genes, Reporter
genetic screens
Genetic Testing
Green Fluorescent Proteins - metabolism
High-Throughput Screening Assays
Humans
Melanoma - genetics
Melanoma - pathology
miR146
Neoplasms - genetics
Neoplasms - pathology
Oncogenes
Protein Kinase Inhibitors - pharmacology
Receptor, Epidermal Growth Factor - metabolism
senescence
senolysis
SMARCB1 Protein - genetics
SOXE Transcription Factors - genetics
SOXE Transcription Factors - metabolism
SWI/SNF
senescence
miR146
SWI/SNF
aurora kinase
genetic screens
compound screen
senolysis
ISSN:2211-1247, 2211-1247
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Shrnutí:Senescence is a proliferation arrest that can result from a variety of stresses. Cancer cells can also undergo senescence, but the stresses that provoke cancer cells to undergo senescence are unclear. Here, we use both functional genetic and compound screens in cancer cells harboring a reporter that is activated during senescence to find targets that induce senescence. We show that suppression of the SWI/SNF component SMARCB1 induces senescence in melanoma through strong activation of the MAP kinase pathway. From the compound screen, we identified multiple aurora kinase inhibitors as potent inducers of senescence in RAS mutant lung cancer. Senescent melanoma and lung cancer cells acquire sensitivity to the BCL2 family inhibitor ABT263. We propose a one-two punch approach for the treatment of cancer in which a drug is first used to induce senescence in cancer cells and a second drug is then used to kill senescent cancer cells. [Display omitted] •CRISPR and chemical screens identify senescence inducers in cancer cells•SMARCB1 knockout induces senescence in melanoma•Aurora kinase inhibition induces senescence in multiple cancer types•Senescent cancer cells become vulnerable to killing by ABT263 Wang et al. find that CRISPR-mediated genetic screens and chemical screens serve as two types of high-throughput methods to identify senescence inducers in cancer cells. They also show that senescent cancer cells can be killed selectively by the BCL2-family inhibitor ABT263, providing a potential sequential drug treatment strategy for cancer.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2211-1247
2211-1247
DOI:10.1016/j.celrep.2017.09.085