Journal
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
Volume 128, Issue 2, Pages 224-233Publisher
WILEY
DOI: 10.1111/bcpt.13487
Keywords
bufalin; cisplatin; HIF-1 alpha; mTOR; ovarian cancer
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Bufalin, extracted from natural product Chansu, has been tested as an antitumour agent in ovarian cancer. It inhibits cell growth and migration by suppressing mTOR activation and HIF-1 alpha induction, potentially enhancing the efficacy of cisplatin in patients.
Ovarian cancer is a severe health threat for women with increased incidence and stymied development in diagnosis and therapy. Drug resistance is still a big challenge. Bufalin is a multi-functional steroid-like compound extracted from natural product Chansu and has been tested as antitumour agent recently. The application and mechanism of bufalin in ovarian cancer remain unclear yet. Bufalin was first examined in ovarian epithelial cancer cell as well as primary ovarian tissue to evaluate its inhibitory activity in cell growth and migration, followed by the validation in xenograft tumour model and the patient samples. Bufalin is well tolerated by normal ovarian tissue at up to 40 mu M and suppresses the cell growth and migration at 10 mu M and xenograft tumour growth at 0.1mg/kg dosage. Bufalin inhibits the mammalian target of rapamycin (mTOR) activation and subsequently decreases hypoxia-induced factor 1 alpha (HIF-1 alpha) level. Overexpression of HIF-1 alpha could abolish the pro-apoptotic and antimigration activity of bufalin in cell culture. Strikingly, low HIF-1 alpha level was correlated with improved responsiveness to cisplatin treatment in ovarian cancer patients. Bufalin was a potent inhibitor of cell growth and migration in ovarian cancer cells through suppression of mTOR activation and HIF-1 alpha induction. Bufalin could be used to enhance the efficacy of cisplatin in ovarian cancer patients.
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