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Oncotarget. 2014 Oct 15;5(19):9514-29.

FOXF1 mediates mesenchymal stem cell fusion-induced reprogramming of lung cancer cells.

Author information

1
Graduate Institute of Biomedical Materials and Engineering, College of Oral Medicine, Taipei Medical University, Taipei 110, Taiwan. Stem Cell Research Center, Taipei Medical University, Taipei 110, Taiwan.
2
Department of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO 80523, USA.
3
Stem Cell Research Center, Taipei Medical University, Taipei 110, Taiwan.
4
Department of Neurosurgery, Taipei Medical University Hospital, Taipei 110, Taiwan. School of Medicine, Taipei Medical University, Taipei 110, Taiwan.
5
Graduate Institute of Biomedical Materials and Engineering, College of Oral Medicine, Taipei Medical University, Taipei 110, Taiwan.
6
Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei 100, Taiwan.
7
Institute of Biochemistry and Molecular Biology, National Yang Ming University, Taipei 112, Taiwan.
8
Wake Forest Institute of Regenerative Medicine, Winston-Salem, NC 27157, USA.
9
Department of Biomedical Engineering, College of Engineering and School of Medicine, Wayne State University, Detroit, MI 48201, USA Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI 48201, USA.

Abstract

Several reports suggest that malignant cells generate phenotypic diversity through fusion with various types of stromal cells within the tumor microenvironment. Mesenchymal stem cell (MSC) is one of the critical components in the tumor microenvironment and a promising fusogenic candidate, but the underlying functions of MSC fusion with malignant cell have not been fully examined. Here, we demonstrate that MSCs fuse spontaneously with lung cancer cells, and the latter is reprogrammed to slow growth and stem-like state. Transcriptome profiles reveal that lung cancer cells are reprogrammed to a more benign state upon MSC fusion. We further identified FOXF1 as a reprogramming mediator that contributes not only to the reprogramming toward stemness but also to the p21-regulated growth suppression in fusion progeny. Collectively, MSC fusion does not enhance the intrinsic malignancy of lung cancer cells. The anti-malignant effects of MSC fusion-induced reprogramming on lung cancer cells were accomplished by complementation of tumorigenic defects, including restoration of p21 function and normal terminal differentiation pathways as well as up-regulation of FOXF1, a putative tumor suppressor. Such fusion process raises the therapeutic potential that MSC fusion can be utilized to reverse cellular phenotypes in cancer.

PMID:
25237908
PMCID:
PMC4253450
DOI:
10.18632/oncotarget.2413
[Indexed for MEDLINE]
Free PMC Article

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