Inhibition of thromboxane synthase induces lung cancer cell death via increasing the nuclear p27
- Department of Surgery, The Chinese University of Hong Kong, Shatin, New Territories (Hong Kong)
- Department of Clinical Oncology, The Chinese University of Hong Kong, Shatin, New Territories (Hong Kong)
- The William Harvey Research Institute, Queen Mary University of London, London (United Kingdom)
The role of thromboxane in lung carcinogenesis is not clearly known, though thromboxane B2 (TXB{sub 2}) level is increased and antagonists of thromboxane receptors or TXA2 can induce apoptosis of lung cancer cells. p27, an atypical tumor suppressor, is normally sequestered in the nucleus. The increased nuclear p27 may result in apoptosis of tumor cells. We hypothesize that the inhibition of thromboxane synthase (TXS) induces the death of lung cancer cells and that such inhibition is associated with the nuclear p27 level. Our experiment showed that the inhibition of TXS significantly induced the death or apoptosis in lung cancer cells. The activity of TXS was increased in lung cancer. The nuclear p27 was remarkably reduced in lung cancer tissues. The inhibition of TXS caused the cell death and apoptosis of lung cancer cells, likely via the elevation of the nuclear p27 since the TXS inhibition promoted the nuclear p27 level and the inhibition of p27 by its siRNA recovered the cell death induced by TXS inhibition. Collectively, lung cancer cells produce high levels of TXB{sub 2} but their nuclear p27 is markedly reduced. The inhibition of TXS results in the p27-related induction of cell death in lung cancer cells.
- OSTI ID:
- 22209830
- Journal Information:
- Experimental Cell Research, Journal Name: Experimental Cell Research Journal Issue: 17 Vol. 315; ISSN 0014-4827; ISSN ECREAL
- Country of Publication:
- United States
- Language:
- English
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