Abstract
It has been demonstrated that potassium channels (K + channels) play significant roles in some malignant phenotypes. Here, we provide the first evidence that treatment with glybenclamide, an ATP-sensitive K + channel blocker, inhibited cell migration in an ovarian clear cell carcinoma cell line, ES-2. Treatment with glybenclamide or knockdown by siRNA targeted against K + channel subunits demonstrated the suppression of ovarian cancer cell invasion, which occurred via inhibition of PDGF-AA secretion. Therefore, our findings suggest that K + channel blockers may be useful chemotherapeutic drugs for blocking the invasiveness of ovarian cancers.
Original language | English |
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Pages (from-to) | 1504-1509 |
Number of pages | 6 |
Journal | FEBS Letters |
Volume | 586 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2012 May 21 |
Keywords
- Glybenclamide
- Ovarian cancer
- Platelet-derived growth factor
- Potassium channel
- Trafficking
- Tumor invasion
ASJC Scopus subject areas
- Biophysics
- Structural Biology
- Biochemistry
- Molecular Biology
- Genetics
- Cell Biology