Unknown,Transcriptomics,Genomics,Proteomics

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The stress kinase MKK7 couples oncogenic stress to p53 stability and tumor suppression


ABSTRACT: Transcriptional profiling of control and MKK7-deficient primary mouse pneumocytes after oncogenic KRasG12 induction Two-condition experiment, MKK7 proficient vs. MKK7 deficient pneumocytes. 3 Biological replicates: 3 control, 3 knock out, independently grown and harvested. 3 technical replicates per array (each sample was hybridized to 3 in-house arrays (47MM, 51MM and 46MM - see HybridisationInfo.xls) for a total of 54 hybridizations).

ORGANISM(S): Mus musculus

SUBMITTER: Daniel Schramek 

PROVIDER: E-GEOD-26763 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications


Most preneoplastic lesions are quiescent and do not progress to form overt tumors. It has been proposed that oncogenic stress activates the DNA damage response and the key tumor suppressor p53, which prohibits tumor growth. However, the molecular pathways by which cells sense a premalignant state in vivo are largely unknown. Here we report that tissue-specific inactivation of the stress signaling kinase MKK7 in KRas(G12D)-driven lung carcinomas and NeuT-driven mammary tumors markedly accelerates  ...[more]

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