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Cancer Research 68, 6533-6540, August 15, 2008. doi: 10.1158/0008-5472.CAN-07-6642
© 2008 American Association for Cancer Research

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Cell, Tumor, and Stem Cell Biology

Octamer 4 Small Interfering RNA Results in Cancer Stem Cell–Like Cell Apoptosis

Tingsong Hu1, Shanrong Liu1, Deborah R. Breiter3, Fang Wang1, Ying Tang2 and Shuhan Sun1

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]







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
Copyright © 2008 by the American Association for Cancer Research.