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Control of alveolar differentiation by the lineage transcription factors GATA6 and HOPX inhibits lung adenocarcinoma metastasis.
- Source :
-
Cancer cell [Cancer Cell] 2013 Jun 10; Vol. 23 (6), pp. 725-38. Date of Electronic Publication: 2013 May 23. - Publication Year :
- 2013
-
Abstract
- Molecular programs that mediate normal cell differentiation are required for oncogenesis and tumor cell survival in certain cancers. How cell-lineage-restricted genes specifically influence metastasis is poorly defined. In lung cancers, we uncovered a transcriptional program that is preferentially associated with distal airway epithelial differentiation and lung adenocarcinoma (ADC) progression. This program is regulated in part by the lineage transcription factors GATA6 and HOPX. These factors can cooperatively limit the metastatic competence of ADC cells, by modulating overlapping alveolar differentiation and invasogenic target genes. Thus, GATA6 and HOPX are critical nodes in a lineage-selective pathway that directly links effectors of airway epithelial specification to the inhibition of metastasis in the lung ADC subtype.<br /> (Copyright © 2013 Elsevier Inc. All rights reserved.)
- Subjects :
- Adenocarcinoma genetics
Adenocarcinoma of Lung
Cell Differentiation
Cell Line, Tumor
Cell Lineage
Cluster Analysis
Epithelium pathology
GATA6 Transcription Factor genetics
GATA6 Transcription Factor metabolism
Gene Expression Regulation
Homeodomain Proteins genetics
Homeodomain Proteins metabolism
Humans
Lung Neoplasms genetics
Neoplasm Invasiveness
Neoplasm Metastasis genetics
Pulmonary Alveoli cytology
Pulmonary Alveoli pathology
Tumor Suppressor Proteins genetics
Tumor Suppressor Proteins metabolism
Adenocarcinoma pathology
GATA6 Transcription Factor physiology
Homeodomain Proteins physiology
Lung Neoplasms pathology
Neoplasm Metastasis pathology
Tumor Suppressor Proteins physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1878-3686
- Volume :
- 23
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Cancer cell
- Publication Type :
- Academic Journal
- Accession number :
- 23707782
- Full Text :
- https://doi.org/10.1016/j.ccr.2013.04.009