miR-375 is activated by ASH1 and inhibits YAP1 in a lineage-dependent manner in lung cancer.
basic_science · Level V
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- Record sourced from PubMed, PMID 21856745.
- Also identified by DOI 10.1158/0008-5472.CAN-11-1020.
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Abstract
Lung cancers with neuroendocrine (NE) features are often very aggressive but the underlying molecular mechanisms remain elusive. The transcription factor ASH1/ASCL1 is a master regulator of pulmonary NE cell development that is involved in the pathogenesis of lung cancers with NE features (NE-lung cancers). Here we report the definition of the microRNA miR-375 as a key downstream effector of ASH1 function in NE-lung cancer cells. miR-375 was markedly induced by ASH1 in lung cancer cells where it was sufficient to induce NE differentiation. miR-375 upregulation was a prerequisite for ASH1-mediated induction of NE features. The transcriptional coactivator YAP1 was determined to be a direct target of miR-375. YAP1 showed a negative correlation with miR-375 in a panel of lung cancer cell lines and growth inhibitory activities in NE-lung cancer cells. Our results elucidate an ASH1 effector axis in NE-lung cancers that is functionally pivotal in controlling NE features and the alleviation from YAP1-mediated growth inhibition.
Medical subject headings
- Adaptor Proteins, Signal Transducing
- Adenocarcinoma
- Basic Helix-Loop-Helix Proteins
- Carcinoma, Small Cell
- Lung Neoplasms
- MicroRNAs
- Phosphoproteins