Oct-3/4 Expression Reflects Tumor Progression and Regulates Motility of Bladder Cancer Cells

Chao-Ching Chang(Institute of Physiology and Basic Medicine), Gia-Shing Shieh(Institute of Clinical Research), Pensée Wu(Imperial College London), Chia-Cheng Lin(Ministry of Health and Welfare), Ai‐Li Shiau(Institute of Physiology and Basic Medicine), Chao‐Liang Wu(Institute of Physiology and Basic Medicine)
Cancer Research
August 1, 2008
Cited by 154

Abstract

Cancer and embryonic stem cells exhibit similar behavior, including immortal, undifferentiated, and invasive activities. Here, we show that in clinical samples bladder tumors with intense expression of stem cell marker Oct-3/4 (also known as POU5F1) are associated with further disease progression, greater metastasis, and shorter cancer-related survival compared with those with moderate and low expressions. Expression of Oct-3/4 is detected in human bladder transitional cell carcinoma samples and cell lines. Overexpression of Oct-3/4 enhances, whereas knockdown of Oct-3/4 expression by RNA interference reduces, migration and invasion of bladder cancer cells. Oct-3/4 can up-regulate fibroblast growth factor-4 and matrix metalloproteinase-2 (MMP-2), MMP-9, and MMP-13 production, which may contribute to tumor metastasis. Finally, we show that Ad5WS4, an E1B-55 kD-deleted adenovirus driven by the Oct-3/4 promoter, exerts potent antitumor activity against bladder cancer in a syngeneic murine tumor model. Therefore, our results implicate that Oct-3/4 may be useful as a novel tumor biological and prognostic marker and probably as a potential therapeutic target for bladder cancer.


Related Papers

No related papers found

Powered by citation graph analysis