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Stem Cells. 2016 Nov;34(11):2613-2624. doi: 10.1002/stem.2447. Epub 2016 Jul 11.

Positive Feedback Loop of OCT4 and c-JUN Expedites Cancer Stemness in Liver Cancer.

Author information

1
Department of Surgery.
2
Center of Stem Cell Research.
3
School of Dentistry.
4
Graduate Institute of Medicine.
5
Welgene Biotech. Inc, Taipei, Taiwan.
6
Department of Physiology, Keio University School of Medicine, Shinanomachi, Tokyo, 160-8582, Japan.
7
RIKEN BioResource Center, Tsukuba, 305-0074, Japan.
8
Saito Laboratory of Cell Technology, Yaita, Tochigi, 329-1571, Japan.
9
Department of Pathology.
10
Department of Biochemistry and Molecular Biology, Rutgers New Jersey Medical School, Rutgers, the State University of New Jersey, Newark, New Jersey, USA.
11
Department of Gastroenterology, Kaohsiung Medical University Hospital, Kaohsiung, 807, Taiwan.
12
Center of Infectious Diseases and Cancer Research.
13
Department of Internal Medicine, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung, 807, Taiwan.
14
Department of Biological Sciences, National Sun Yat-sen University, Kaohsiung, 804, Taiwan.
15
Research Center for Environmental Medicine, Kaohsiung Medical University, Kaohsiung, 807, Taiwan.
16
Faculty of Science and Engineering, Tokushima Bunri University, Sanuki, 763-2193, Japan.
17
Department of Molecular Preventive Medicine, Graduate School of Medicine, the University of Tokyo, Tokyo, 113-0033, Japan.

Abstract

The network of stemness genes and oncogenes in human patient-specific reprogrammed cancer stem cells (CSCs) remains elusive, especially in liver cancer. HepG2-derived induced pluripotent stem cell-like cells (HepG2-iPS-like cells) were generated by introducing Yamanaka factors and the knockdown vector shTP53. They exhibited features of stemness and a higher tumorigenesis after xenograft transplantation compared with HepG2 cells. The cancerous mass of severe combined immunodeficiency (SCID) mice derived from one colony was dissected and cultured to establish reprogrammed HepG2-derived CSC-like cells (designated rG2-DC-1C). A single colony exhibited 42% occurrence of tumors with higher proliferation capacities. rG2-DC-1C showed continuous expression of the OCT4 stemness gene and of representative tumor markers, potentiated chemoresistance characteristics, and invasion activities. The sphere-colony formation ability and the invasion activity of rG2-DC-1C were also higher than those of HepG2 cells. Moreover, the expression of the OCT4 gene and the c-JUN oncogene, but not of c-MYC, was significantly elevated in rG2-DC-1C, whereas no c-JUN expression was observed in HepG2 cells. The positive-feedback regulation via OCT4-mediated transactivation of the c-JUN promoter and the c-JUN-mediated transactivation of the OCT4 promoter were crucial for promoting cancer development and maintaining cancer stemness in rG2-DC-1C. Increased expression of OCT4 and c-JUN was detected in the early stage of human liver cancer. Therefore, the positive feedback regulation of OCT4 and c-JUN, resulting in the continuous expression of oncogenes such as c-JUN, seems to play a critical role in the determination of the cell fate decision from iPS cells to CSCs in liver cancer. Stem Cells 2016;34:2613-2624.

KEYWORDS:

Cancer stem cells; Liver cancer; OCT4; Pluripotency; Positive feedback; Reprogramming; c-JUN

PMID:
27341307
DOI:
10.1002/stem.2447
[Indexed for MEDLINE]
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