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IMR90 ER:RAS: A cell model of oncogene-induced senescence
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Title: | IMR90 ER:RAS: A cell model of oncogene-induced senescence |
Authors: | Innes, AJ Gil, J |
Item Type: | Journal Article |
Abstract: | Oncogene-induced senescence (OIS) is a cellular response that limits the replication of cells expressing oncogenes. As a result, OIS is a potent tumor suppressor mechanism limiting cancer progression. Here we describe IMR90 ER:RAS, a widely used model to study OIS in cell culture. This model takes advantage of IMR90 human primary fibroblast infected with a 4-hydroxy-tamoxifen (4-OHT) inducible ER:RAS construct. RAS activation upon 4-OHT treatment results in a coordinated induction of senescence, recapitulating different aspects of the phenotype such as the growth arrest and the establishment of a senescence-associated secretory phenotype (SASP). |
Issue Date: | 31-Jan-2019 |
Date of Acceptance: | 1-Jan-2019 |
URI: | http://hdl.handle.net/10044/1/65506 |
DOI: | https://dx.doi.org/10.1007/978-1-4939-8931-7_9 |
ISSN: | 1940-6029 |
Publisher: | Humana Press |
Start Page: | 83 |
End Page: | 92 |
Journal / Book Title: | Methods in Molecular Biology |
Volume: | 1896 |
Copyright Statement: | © 2019 Springer Science+Business Media, LLC, part of Springer Nature. The final publication is available at Springer via https://dx.doi.org/10.1007/978-1-4939-8931-7_9 |
Keywords: | BrdU Growth arrest Oncogene-induced senescence SASP Senescence p16INK4a p21CIP1 p53 0601 Biochemistry And Cell Biology Developmental Biology |
Publication Status: | Published |
Conference Place: | United States |
Appears in Collections: | Department of Medicine (up to 2019) |