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pmid:26697357

Gene expression analysis of microtubule affinity-regulating kinase 2 in non-small cell lung cancer.

Erin A Marshall · Kevin W Ng · Christine Anderson · Roland Hubaux · Kelsie L Thu · Wan L Lam · Victor D Martinez

Genomics data · 2015 doi:10.1016/j.gdata.2015.08.011

Paper

complete

Experiment

partial

Data

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Analysis

partial

Execution

absent

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Gene expression analysis of microtubule affinity-regulating kinase 2 in non-small cell lung cancer.
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10.1016/j.gdata.2015.08.011
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Erin A Marshall
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Kevin W Ng
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Christine Anderson
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Roland Hubaux
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Kelsie L Thu
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Victor D Martinez
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2015
abstract
Lung cancer is the leading cause of cancer death worldwide, and has a five-year survival rate of 18% [1]. MARK2 is a serine/threonine-protein kinase, and is a key component in the phosphorylation of microtubule-associated proteins [2], [3]. A recent study published by Hubaux et al. found that microtubule affinity-regulating kinase 2 (MARK2) showed highly frequent DNA and RNA level disruption in lung cancer cell lines and independent non-small cell lung cancer (NSCLC) cohorts [4]. These alterations result in the acquisition of oncogenic properties in cell lines, such as increased viability and anchorage-independent growth. Furthermore, a microarray-based transcriptome analysis of three short hairpin RNA (shRNA)-mediated MARK2 knockdown lung adenocarcinoma cell lines (GEO#: GSE57966) revealed an association between MARK2 gene expression and cell cycle activation and DNA damage response. Here, we present a detailed description of transcriptome analysis to support the described role of MARK2 in promoting a malignant phenotype.
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