MED12 controls the response to multiple cancer drugs through regulation of TGF-β receptor signaling

Inhibitors of the ALK and EGF receptor tyrosine kinases provoke dramatic but short-lived responses in lung cancers harboring EML4-ALK translocations or activating mutations of EGFR, respectively. We used a large-scale RNAi screen to identify MED12, a component of the transcriptional MEDIATOR complex...

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Vydáno v:	Cell Ročník 151; číslo 5; s. 937
Hlavní autoři:	Huang, Sidong, Hölzel, Michael, Knijnenburg, Theo, Schlicker, Andreas, Roepman, Paul, McDermott, Ultan, Garnett, Mathew, Grernrum, Wipawadee, Sun, Chong, Prahallad, Anirudh, Groenendijk, Floris H, Mittempergher, Lorenza, Nijkamp, Wouter, Neefjes, Jacques, Salazar, Ramon, Ten Dijke, Peter, Uramoto, Hidetaka, Tanaka, Fumihiro, Beijersbergen, Roderick L, Wessels, Lodewyk F A, Bernards, René
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	United States 21.11.2012
Témata:	Antineoplastic Agents - therapeutic use Carcinoma, Non-Small-Cell Lung - drug therapy Drug Resistance, Neoplasm Epithelial-Mesenchymal Transition Humans Lung Neoplasms - drug therapy MAP Kinase Signaling System Mediator Complex - genetics Mediator Complex - metabolism Neoplasms - drug therapy Receptors, Transforming Growth Factor beta - metabolism Signal Transduction
ISSN:	1097-4172, 1097-4172
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