| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Cell, Tumor, and Stem Cell Biology |
1 Department of Medical Genetics and 2 Institute of Biophysics, Second Military Medical University, Shanghai, China; and 3 Department of Biochemistry and Chemistry, Rockford College, Rockford, Illinois
Requests for reprints: Shanrong Liu and Shuhan Sun, Department of Medical Genetics, Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, China. Phone: 86-21-25070331; Fax: 86-21-25070331; E-mail: liushanrong{at}hotmail.com (S. Liu) and shsun{at}vip.sina.com (S. Sun).
Key Words: Oct4 stem cell tumor
Octamer 4 (Oct4), a member of the POU family of transcription factors, plays a key role in the maintenance of pluripotency and proliferation potential of embryonic stem cells. Cancer stem cell–like cells (CSCLC) are reported to be a minor population in tumors or even in tumor cell lines which also express Oct4. The role of Oct4 in CSCLCs still remains to be defined. In our study, we show that, in vitro, almost all murine Lewis lung carcinoma 3LL cells and human breast cancer MCF7 cells express Oct4 at high levels. This expression of Oct4 is successfully reduced by small interfering RNA, which eventually results in cell apoptosis. The signal pathway Oct4/Tcl1/Akt1 has been observed to be involved in this event. The repression of Oct4 reduces Tcl1 expression and further down-regulates the level of p-Ser.473-Akt1. In vivo, only
5% of tumor cells were detected to express Oct4 in established 3LL and MCF7 tumor models, respectively. Small interfering RNA against Oct4 successfully decreases the CSCLCs and markedly inhibits tumor growth. In summary, we show that Oct4 might maintain the survival of CSCLCs partly through Oct4/Tcl1/Akt1 by inhibiting apoptosis, which strongly indicates that targeting Oct4 may have important clinical applications in cancer therapy. [Cancer Res 2008;68(16):6533–40]
This article has been cited by other articles:
![]() |
C. R. Jeter, M. Badeaux, G. Choy, D. Chandra, L. Patrawala, C. Liu, T. Calhoun-Davis, H. Zaehres, G. Q. Daley, and D. G. Tang Functional Evidence that the Self-Renewal Gene NANOG Regulates Human Tumor Development Stem Cells, May 1, 2009; 27(5): 993 - 1005. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Karoubi, M. Gugger, R. Schmid, and A. Dutly OCT4 expression in human non-small cell lung cancer: implications for therapeutic intervention,, Interactive CardioVascular and Thoracic Surgery, April 1, 2009; 8(4): 393 - 397. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Cancer Research | Clinical Cancer Research |
| Cancer Epidemiology Biomarkers & Prevention | Molecular Cancer Therapeutics |
| Molecular Cancer Research | Cancer Prevention Research |
| Cancer Prevention Journals Portal | Cancer Reviews Online |
| Annual Meeting Education Book | Meeting Abstracts Online |